Beruflich Dokumente
Kultur Dokumente
AIPMT Syllabus
1. Introduction
2. Spermatogenesis
3. Structure of sperm
Oogenesis
5. types of Egg
6. Fertilisation
7. Parthenogenesis
9. Implantation
Exercise # 1…….………………………………….209
Exercise # 2 …….…………………………………049
*** Students are advised to solve the questions of exercises in the same sequence or as
directed by the faculty members.
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1
Index : Preparing your own list of Important/Difficult Questions
Instruction to fill
(A) Write down the Question Number you are unable to solve in column A below, by Pen.
(B) After discussing the Questions written in column A with faculties, strike off them in the
manner so that you can see at the time of Revision also, to solve these questions again.
(C) Write down the Question Number you feel are important or good in the column B.
COLUMN :A COLUMN :B
EXERCISE NO.
Questions I am unable
Good/Important questions
to solve in first attempt
Exercise # 1
Exercise # 2
Advantages
1. It is advised to the students that they should prepare a question bank for the revision as it is
very difficult to solve all the questions at the time of revision.
2. Using above index you can prepare and maintain the questions for your revision.
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EMBRYOLOGY
INTRODUCTION :
Embryology is the branch of biology which involves the study of all those processes, which take place
during the development of an adult from the egg.
FORMATION OF GAMETES :
Follicle stimulating hormone stimulates gametogenesis. Besides this hormone vitamin E is also essential
for gametogenesis. Deficiency of vitamin E leads to sterility. Vitamin A is also required for the
formation of healthy gametes.
Gemetogenesis is divided in three stages :
As there are two types of gametes, the spermatozoa and ova, gametogenesis can be studied under two
broad headings : spermatogenesis and oogenesis. Spermatogenesis is the formation of spermatozoa,
whereas oogenesis is the formation of ova. Both spermatozoa and ova originate from primordial germ
cells or PGCs, which are extra-gonadal in origin. In humans, the PGCs originate during early
embryonic development from the extra-embryonic mesoderm. Eventually, they migrate to the yolk sac
endoderm, and ultimately, to the gonads of the developing embryo, where they undergo further
development. You can recall that spermatogenesis occurs in the seminiferous tubules of the testes of
oogenesis occurs in the follicles of ovary. Formation of gametes starts at puberty.
SPERMATOGENESIS :
Spermoatogenesis : i.e. formation of sperms. In most of the animals spermatogenesis takes place in
testes, (exception-earthworm). Mammalian testes contain seminiferous tubules and wall of seminiferous
tubule is composed of germinal epithelium. It contains some special types of cells called primordial
germ cells and these cells start spermatogenesis. On the basis of origin, primordial germ cells are extra
embryonic mesodermal. Besides these cells, germinal epithelium contains some large sized cell called
sertoli cells. Occurrence of sertoli cells is the unique feature of mammalian testis. Sertoli cells provide
nutrition of developing sperm i.e. developing sperms are embedded in cytoplasm of sertoli cells and
absorb nutrition. After maturation sperms comes out from sertoli cells and librate in seminiferous
tubules.
Mammalian sperms are transferred to vagina of female by the process called insemination.
Sertoli cells form 'blood testes barrier' and protect the sperm from immune system of the body. because
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antibody may attach on haploid cells and destroy them. (Sperms are haploid and other cells of body are
diploid).
Sertoli cells function as an endocrine gland i.e. secrete three type of hormones :
(i) Antimullerian hormone : function of this hormone is degradation of female gonads in male embryo.
(In male seminal vesicle is the ruminant part of oviduct of female).
(ii) Inhibin hormone : Function of this hormone is to control excess secretion of pituitary gland
to prevent the over-production of sperms.
(iii) Androgen binding protein : Function of this hormone is to concentrate testosterone in seminiferous
tubules because testosterone is must for spermatogenesis in seminiferous tubules.
STEPS OF SPERMATOGENESIS :
Spermatozoa are formed in the wall of the seminiferous tubules of the testes. The various cell-stages in
spermatogenesis are as follows (the number of chromosomes at each stage is given in brackets)
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An adult male produces over 1012 to 1013 sperm cells each day. These gradually move into the
epididymis and the first portion of the vas deferens, where they undergo further maturation and are
stored.
A. The spermatogonia (type A) or germ cells (44 X + Y) divide mitotically, to give rise to more
spermatogonia of type A (spermatogenic lineage) and also spermatogonia of type B.
C. The primary spermatocytes (44 + X + Y) now divide so that each of them forms two secondary
spermatocytes. This is the first meiotic division. it reduces the number of chromosomes to half.
E. Each spermatid (22 + X or 22 + Y) gradually changes its shape to become a spermatozoon. This process
of transformation of a circular spermatid to a spermatozoon is called spermiogenesis/spermateleosis
Spermiogenesis
In spermiogenesis first, of all nucleus of spermatid shift at one side. Except chromatin material, all
the structures come out from nucleus as a result nucleus become small and light in weight. Then several golgi
vesicles gathered just above the nucleus. Some of the Golgi vesicles develop granules called
proacrosomal granules, such granule containing vesicle is called proacroblast. Rest of the golgi
vesicles are called golgirest, the golgirest dissolve in cytoplasm. All the proacroblast fuse and form large
vesicle called acroblast and it's granule is called acrosomal granule. Acroblast arranged just above the
nucleus. Then cytoplasm of spermatid starts moving towards posterior side. As a result, plasma membrane
shrinks and gets attached to acroblast and nucleus. Due to this head of sperm is formed. Now centriole starts
forming axonema, then all the mitochondria of spermatid are arranged in spiral order around axonema. In
this way middle piece of sperm is formed. Now axonema elongates towards posterior side and forms tail.
Cytoplasm of spermatid continuously flows towards posterior side.
Structure of sperm :
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The spermatozoon has a head, a middle piece and a tail. The head is covered by cap the acrosomic cap,
anterior nuclear cap, or galea capitis. Acrosome is a bag like structure filled with lytic enzymes called
spermlysins. In the anterior part of middle piece neck is present. The neck is narrow : it contains a
proximal & distal centriole (or Basal body). An axial filament begins just behind this centriole, it passes
through the middle piece and extends into the tail. At the point where the middle piece joins the tail, this
axial filament passes through a ring-like structure called the annulus (or ring centriole or zensons ring).
That part of the axial filament which lies in the middle piece, is surrounding by a spiral sheath made up
of mitochondria. (Nebenkern sheath)
HEAD
Nucleus forms Head
NECK
Mitochondria form the a heath
of the Midpiece
MIDDLE PIECE
Proximal centriole comes to lie
in the neck
Nuclear part of head of spermatozoa consist of chromatin (mostly DNA) that is extremely condensed. It
contains a basic nature protein called protamin.
The basal body is made up of nine segmented rod like structures each of which is continuous distally
with one coarse fibril of the axial filament.
The axial filament, that passes through the middle piece and most of the tail, is actually composed of
several fibrils arranged. There is a pair of central fibrils, surrounded by nine pairs (doublets) arranged in
a circle around the central pair (9+ 2). This arrangement of one central pair of fibrils surrounded by nine
doublets is covered by nine solid protein (making the arrangement as 9 + 9+ 2).
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STRUCTURE OF A MATURE SPERMATOZOA
Structure of sperm
In the proximal tail part it is covered by only two solid protein fibres (therefore arrangement is 2 + 9 + 2),
while end part of tail has no protein covering (therefore arrangement is 9 +2). Immediately outside the
fibrils there is a fibrous health.
Middle piece (also called as the energy chamber) is surrounded by spirally arranged mitochondria
(Nebenkern sheath). Finally, the entire sperm is enclosed in a plasma membrane.
OOGENESIS :
Fig. 2
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Like spermatogenesis oogenesis process also can be divided into three stages :
(A) Multiplication (B) Growth phase (C) Maturation phase
(A) Multiplication phase : In this stage primordial germ cells or ovum mother cells repeatedly divide by
mitosis to form large number of diploid oogonia.
This process completes in embryo stage of female in most higher animals.
(B) Growth phase : Like spermatogenesis, in this process oogonia grow in size and form primary oocytes.
The growth phase is the longest phase oogenesis (except humans). During growth phase size of egg
increases many times.
During growth phase several changes occur in egg and all these changes are classified in 2 sub-stages
– Previtellogenesis
– Vitellogenesis
Previtellogenesis :
Activity of DNA increases in nucleus, as a result DNA become highly active and rapidly synthesizes
different types of RNA. Increased activity of DNA is called as Gene redundancy/Gene amplification.
Due to all these changes, size of nucleus increases and nucleus becomes vesicular. This vasicular nucleus is
called germinal vesicle .
Changes in cytoplasm :
In cytoplasm, rate of protein synthesis increases. Cytoplasm rapidly synthesises different type of protein
and enzyme. Due to more availability of protein and enzymes, synthesis of new protoplasm takes place
and size of egg increases.
Number of cell organelles increase in cytoplasm, specially endoplasmic reticulum, golgi-body and mitochondria
Mitochondria become very large in number so mitochondrial clouds are found in cytoplasm of egg.
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Later on all these 3 cell organelle (golgi body, endoplasmic reticulum, mitochondria) are arranged in the
form of ring around the nucleus, it is called as Balbiani vitelline ring. In the stage golgi body of egg
secretes a membrane around the egg which is it called as vitelline membrane. A space appears in
between plasma membrane of egg and vitelline membrane called as perivitelline space, It is filled with a
fluid called perivitelline fluid.
At the end of previtellongenesis endoplasmic reticulum disappear. Golgi bodies gets converted into
corticle granule. Corticle granules are filled with mucopolysacharide. Large number of change occur in
mitochondria also.
So mitochondria of egg with the help of kinase enzyme make the yolk more viscous and insoluble.
2 types of yolk is found :
(C) Maturation phase : Oogenesis (Fig. 2) takes place in the ovaries. In contrast to males the initial
steps in egg production occur prior to birth. By the time the foetus is 25 weeks old, all the oogonia
that she will ever produce, are already formed by mitosis. Hundreds of these diploid cells develop
into primary oocytes, begin the first steps of the first meiotic division, proceed up to diakinesis,
and them stop any further development. The oocytes grows much larger and completes the meiosis
I, forming a large secondary oocyte and a small polar body that receives very little amount of
cytoplasm but one full set of chromosomes.
In humans (and most vertebrates), the first polar body does not undergo meiosis II, whereas the
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secondary oocyte proceeds as far as the metaphase stage of meiosis II. However, it then stops
advancing any further, it awaits the arrival of the spermatozoa for completion of second meiotic
division. Entry of the sperm restarts the cell cycle breaking down MPF (M-phase promoting factor
and turning on the APC (Anaphase promoting complex). Completion of meiosis II converts the
secondary oocyte into a fertilized egg or zygote (and also a second polar body)
Ova are derived from oogonia present in the cortex of ovary. Some important differences between
oogenesis and spermatogenesis are
(i) Whereas one primary spermatocyte gives rise to four spermatozoa, one primary oocyte forms only one
ovum.
(ii) When the primary spermatocyte divides, its cytoplasm is equally distributed between the two secondary
spermatocytes formed. However, when the primary occyte divides, almost all its cytoplasm goes to the
daughter cell which forms the secondary oocyte. The other daughter cell (first polar body), receives half
the chromosomes of the primary oocyte, but almost no cytoplasm.
The first polar body is, therefore, formed merely to get rid of unwanted chromosomes.
TYPES OF EGGS :
- The amount of yolk is very small or absent in these types of eggs. (oligolecithal, or microlecithal or
alecithal).
- The term 'alecithal' (absence of yolk eg. Man) was given by Kent. And term microlecithal' (eg.
Urchin) was given by Tori.
Examples :- Egg of Amphioxus, Eutheria, Metatheria and sea – urchin.
(ii) Mesolecthal Eggs : - In this type of egg, the amount of yolk is moderate i.e medium ,neither more
nor less.
Example : - Eggs of Amphibia, Petromyzon and lung-fishes.
(i) Isolecithal or homolecithal eggs : The yolk is evenly or homogenously distributed in these eggs.
eg. : micro, oligo or alecithal eggs.
(ii) Telolecithal eggs : The yolk is concentrated in one part of the egg.
eg. Mesolecithal eggs of amphibia. (Moderately telolecithal)
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Discoidal eggs : A type of telolecithal and megalecithal eggs. Where the yolk is in enormous quantity
and concentrated in one part of the egg. Thus only a disc of cytoplasm called germinal disc remains
in the egg which is located at the other pole of egg. (Heavily telolecithal)
eg. : Eggs of reptiles, birds and prototherian mammals.
(iii) Centrolecithal eggs : Megalecithal eggs where the enormous amount of yolk is located in the
centre an cytoplasm is in the form of superficial layer around the yolk.
eg. : Insects egg.
(C) Classification of Eggs on the basis of Shell : -
On the basis of shell, eggs are of 2 types : -
(i) Cleidoic eggs : -
Eggs surrounded by a hard shell are known as cleidoic eggs. These eggs are found in those animal
which have a terrestrial mode of life or which lay eggs on land.
These eggs have more amount of yolk. These are adaptations to terrestrial mode of life. Shell
prevents the egg from dessication.
e.g. : - eggs of ''Reptiles'', ''Birds'', ''Insects'' and ''Prototherians''.
(ii) Non-Cleidoic eggs : -
Eggs which are not surrounded by a hard shell are called non-cleidoic eggs.
eg. : - all viviparous animals (Mammals) and all oviparous animals which lay eggs in water
(Amphibians). Reptilia eggs are called leathery eggs.
STRUCTURE OF AN OOCYTE :
The nucleus of egg is also called germinal vesicle.
Majority eggs are oval but the eggs of insects are long and cylindrical. Smallest eggs are of 50 in
polychaeta and the largest eggs are of an Ostrich.
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Functions of Egg-membranes
(i) To provide protection (ii) To check polyspermy (iii) To provide buoyancy to the amphibian eggs
Eggs of insects are megalecithal or polylecithal in them yolk is present in the centre, so the eggs are
also centrolecithal.
Two egg membranes are present here, inner vitelline membrane (primary) and outer chorian (secondary).
The sperm enters the egg through micropyle because on the head of insect sperm acrosome is absent.
Frog's Egg
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Two types of egg membranes are found in frogs egg :
(i) Vitelline membrane : This is primary egg membrane which is secreted by the ovum around itself.
(ii) Jelly coat : This is tertiary egg membrane, secreted by oviduct. Jelly coat has air bubbles trapped in
it due to which it floats on water. This group of frogs egg is called spawn, Jelly coat is bitter in taste
so enemies do not eat it.
(i) Animal pole : This part has cytoplasm, egg nucleus in also located in this part. In the cytoplasm
melanin granules are found which prevent the egg from harmfull radiations. They also help in
protection of egg by camouflage.
A sperm always enters into the ovum at some point in animal hemisphere. This point is normally other
than the animal pole itself.
As the sperm enters into the ovum, taking some pigment granules with it, a grey, crescent shaped region
appears in the equatorial zone geometrically opposite the sperm entrance point. This region is called
grey crescent. It is formed due to movement of some pigment granules away from it towards sperm
entrance point.
(It marks the dorsal side of future embryo). This area of sperm entrance point marks the anterior side of
future embryo. The side diagonally opposite to it in the vegetal hemisphere marks the future posterior
side. Thus the sperm entrance establishes the anteroposterior and dorsoventral axis as well as bilateral
symmetry of future embryo.
In these eggs, yolk is present in the centre of the egg in the form of a dense mass. The cytoplasm of the
egg is in the form of a disc above the yolk, which is termed as the germinal-disc.
Yellow – yolk has more amount of phospholipids and is secreted during the night. White yolk has less
amount of phospholipids and is secreted during the day time. Central white part of yolk is called latebra.
Both the types of yolk are arranged in alternate and concentric layers.
Pander was the scientist, who discovered the 3 germinal layers i.e. Ectoderm Mesoderm and Endoderm
in chick - egg.
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Chick Egg
Around the egg, porous shell of CaCO3 is present which is secreted by the cells of the oviduct.
In between the vitelline membrane and the shell membrane albumin is filled which is also called the
white of egg. It contains 13% proteins.
Thick albumin-fibres termed as ''Chalaza'' are present in the albumin part of egg.
Mammalian eggs have very less amount of yolk, so the eggs are oligolecithal and isolecithal or
microlecithal and homolecithal.
(1) Zona Pellucida : - This is a transparent membrane like covering and is a primary membrane
secreted by the ovum/oocyte itself.
(2) Corona radiata : - This is a layer of follicular cells'' and these cells are attached to the surface of
egg through ''hyaluronic acid'' This is a secondary membrane, which is secreted by the ovary. These
eggs don't have tertiary membrane.
Mammalian eggs are approx 0.1 mm in size.
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FERTILIZATION :
The process in which union of male and female gametes (formed by gametogenesis) and fusion of
pronuclei of sperm and ovum takes place thus diploid zygote is formed, is called fertilization.
Fertilization has following processes : - The union of male and female gametes is called Syngamy.
Where as intermixing of their cytoplasm is called plasmogamy. The fusion of pronuclei of sperm and
ovum is called karyogamy. The intermingling of their chromosomes is called amphimixis.
Due to fertilization , a diploid zygote is formed, by the union of two different types of gametes.
SITE OF FERTILIZATION :
(A) INTERNAL FERTILIZATION - Fertilization in the body (i.e., genital organs of animal) is called
internal fertilization. In this type of fertilization, sperms are discharged by male directly into the genital
tract of female after coitus.
- Whole process of fertilization takes place within the body of female. This is the most common
adaptation in terrestrial animals.
Examples : - Aschelminthes, reptiles, birds and mammals.
(B) EXTERNAL FERTILIZATION - External fertilization takes place outside the body of females i.e., in
water.
Example : - In most of the invertebrates, some protochordates, amphibian and most of the fishes.
TYPES OF FERTILIZATION :
(a) Self fertilization - This process takes place in the body of single animal i.e., fusion of male and female
gametes produced by male and female organs of the same animal. This is called self-fertilization. This is
possible only in bisexual or hermaphrodite animals.
Examples : - Animals of phylum porifera and most of the species Hydra.
(b) Cross-Fertilization – Fertilization takes place between two (male & female) different animals of same
species.
This is called cross fertilization.
- This process is found in all unisexual animals. These animals are also called dioecious animals
- Cross-fertilization is also found in most of the bisexual or hermaphrodite animals because in these
animals male genital organs develop first. This condition is called protandrous condition. In some of the
species female organs develop first, this condition is called protogynous condition e.g. sponges.
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Approach of sperm towards the egg – it is a chance factor, so sperms perform random (directionalless)
movement. To increase the chances of approach of sperm towards egg there are mainly two adaption
(a) Number of sperms is very high : - e.g. In man 20 to 120 million sperms are present per cubic mm
of semen.
- Some special proteins are found on the surface of egg and sperm to help in fertilization.
According of Lillie, chemicals named as ''fertilizins'' are found on the surface of egg. Fertilins are
glycoproteins or acid mucopolysaccharides. According to Ballinsky, an acidic protein named as
Antifertilizin is present on the surface of sperms. ''Fertilin'' proteins are also present on sperm surface.
- Both the proteins are specific for a particular species. Antifertilizin present on sperm of a particular
species will react with fertilizin of present on egg of the same species of animals.
- If we place some eggs of sea-urchin in sea-water, this sea water becomes viscous, this is called egg-
water. When some sperms come in contact with this egg water, sperms adhere with each other. It is
called agglutination.
Here the reaction of fertilizin (dissolved in water from egg) and antifertilizin of sperm is observed
clearly.
- According to Washerman and Sailing (1989) a specific pair of protein molecules is found on the surface
of mammalian sperm, which can recognize specific carbohydrates and proteins in ZP 3 region of zona
pellucida. The bindin protein of sperm reacts with these molecules to initiate the changes in acrosome.
A specific sugar galactose remains attached with ZP3 glycoprotein. The sperm fails to recognize the
ovum of its own species, if this sugar is removed from zona pellucida.
- In addition to these glycoproteins, there are some hormones also, which help in fertilization.
The hormones present at the surface of sperm are called androgamones. These are of two types.
Androgamone first & androgamone second.
- Androgamones II dissolve the gelatinous coverting present all over the egg.
- Hormones present at the surface of egg are called gyanogamones these are of 2 types.
(a) Gyanogamones I - this hormone neutralizes Androgamone I and activates sperm to move
Enzyme of acrosome (Hyaluronidase and sperm lysins) dissolve the egg membrane. This is called
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acrosomal reaction. As a result sperm head make the contact with the plasma membrane of egg, now
inner membrane of acrosome evaginates outside and form rigid tube is called acrosomal filament.
Acrosomal filament provide stimulus to plasma membrane of egg and due to stimulus of sperm, egg is
induce for fertilization. Mammalian sperms do not form this type of filament because mammalian sperms are
highly active and provide stimulus to plasma-membrane of egg without any filament. Mammalian sperms
acquire activity at two places. First-epididymis and second-vagina. Vaginal secretion make the sperm highly
active and sperm acquire capacity of fertilization is called capacitation.
Activation of egg : Due to stimulus of sperm an enzyme is induced in plasma-membrane of egg it
is called adenyl cyclase enzyme and function of this enzyme is to catalyze C-AMP in egg cytoplasm.
C-AMP is the second messenger. Cyclic AMP receive stimulus from plasma membrane of egg and
transfers it in egg cytoplasm and induces all the response of egg for sperm.
All the response of egg for sperm are collectively called gyanogenesis.
Due to stimulus of sperm, permeability of plasma membrane of egg increases specially for k+ and Ca2+
ions. Function of Ca2+ ions is to inactivate the cytostatic factors in egg. As a result egg is now ready for
cleavage (In egg cytoplasm special type of protein called cytostatic factor are present these factor
prevent the cleavage in unfertilized egg)
Due to stimulus of sperm, H+ – Na+ pump activates and induces the plasma-membrane of egg. Function
of this pump is to continuously influx H+ ions and outflux Na+ ions. As a result concentration of H+ ion
increases in egg cytoplasm and develops an acidic medium. In acidic medium, proteolytic enzyme
become active and liberate the m-RNA from informosome. These m-RNA become active and rapidly
synthesize different types of protein and enzymes. Due to more availability of protein and enzymes
metabolic activity of egg increases.
Response of egg : (1) Due to stimulus of sperm, meiosis-II is induced in human egg by excluding
second polar body becoming mature ovum.
(2) At the point of contact with sperm and plasma-membrane of egg a cone-like structure is formed
called reception cone. After some time reception cone sinks in egg cytoplasm along with sperm
(entry of sperm is a type of phagocytosis). With the entry of sperm all the cortical granules burst and
secrete a membrane around the egg is called fertilization membrane (cortical reaction). It is
secreted on inner surface of primary egg membrane and perivitelline space become more wide and
amount of perivitelline fluid is also increase. Function of perivitelline fluid and fertilization
membrane is to prevent the entry of sperm in egg. so normally only one sperm enter inside the egg
(monospermy). Sometimes more than one sperm enter inside the egg (polypermy). Two types of
polyspermy are found in nature.
(1) Pathological polyspermy : In it the nuclei of all the sperms fuse with egg nucleus. In such type of
condition embryo development does not occur. (Due to polyploidy condition)
(2) Physiological polyspermy : In physiological polysermy nucleus of only one sperm fuses with egg
nucleus and rest of the sperm die in egg cytoplasm. Dead sperm are called merocytes. In
physiological polyspermy normal embryo development occurs.
Polyspermy is absent in human beings. Polyspermy mostly occurs in megalecithal eggs.
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Fate of sperm in egg - In majority of animals, only head and middle piece enter inside the egg and tail
is left outside.
- In mammals, whole sperm enters in the egg.
- In some animals, only head of sperm enters in the egg tail and middle piece remain outside
e.g. Hydra, Neries etc. After entering inside the egg, sperm rotates by 180°. All the structure of sperm
dissolve in egg cytoplasm except sperm nucleus and proximal centriole.
- The centriole of egg itself degenerates at the time of second maturation division. So proximal
centriole of sperm starts division, it divides into 2 daughter centrioles, which migrate towards
opposite pole and start forming spindles.
Fat of sperm nucleus : -
- The nucleus of sperm absorbs water from egg cytoplasm and becomes enlarged. Now it is called
male pronucleus.
After meiosis – II egg nucleus occur in the form of scattered vesicles then it is called as karyomeres and
after some time ll the karyomeres assembled to form complete nucleus is called female pronucleus.
- Male pronucleus and female pronucleus migrate through definite routes and come close to each
other. These routes are called fertilization path. (It has following parts)
(1) Sperm penetration path - Male pronucleus for some distance, moves at the equator of egg. This is
called sperm penetration path.
(2) Sperm copulation path - Male pronucleus starts migrating towards female pronucleus.
(3) Egg copulation path - Female pronucleus migrates towards male pronucleus. Both the pronuclei come
close to each other.
(4) Cleavage path - Both the pronuclei move together to their final position which is somewhere in animal
pole. At this final position nuclear membrane of both the pronuclei degenerate and chromosomes of
male and female pronuclei form pairs. The mixture of male and female chromosomes is called
amphimixis.
- Amphimixis was discovered by O.Hertwig in the eggs of sea – urchin.
- Newport was of all first observed the entry of sperm into the egg.
Significance of Fertilization
1. Oocyte completes its second maturation division on coming in contact with the sperm.
2. Amphimixis process leads to the formation of diploid zygote to restore the normal diploid number of the
chromosomes.
3. The centriole of sperm after entering into egg induces the egg to undergo cleavage.
4. The paternal and maternal characters are transmitted to the off springs through the process of
fertilization.
5. The peripheral changes occurring in the egg prevent the further entry of sperm into the ovum, thus
checking polyspermy.
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PPARTHENOGENESIS OR VIRGINAL DEVELOPMENTT
- The development of embryo without fertilization is called parthenogenesis. The animals which are
formed by unfertilized eggs are called parthenotes.
- The discovery of parthenogenesis was done by Charles Bonet in the eggs of sea-urchins.
Some animals show parthenogenesis by nature e.g. Honey bees, wasps, ants, grass-hoppers, ticks, mites
and sea-urchins. Natural parthenogenesis is of 2 types : -
(i) Haploid parthenogenesis or Arrhenotoky : - In this case eggs are formed by meiosis. Eggs are
haploid, they have the power of fertilization sometimes male animals are developed by unfertilized
eggs. In Honeybees, unfertilized eggs develop into males (drones), and fertilized eggs develop into
queen and soldiers. Thus male honey bees are always haploid and queen with soldiers are always
diploid.
(ii) Diploid parthenogenesis or Thelytoky : - In this case, eggs are formed without meiosis division.
Eggs are diploid they do not have the power of fertilization.
Diploid eggs give rise to female generation only. Male members are absent in these species.
Examples : - Lacerta sexicola armenica (lizard), Caresius aratus gibelio (Fish).
(A) Ameiotic Thelytoky - In this type of parthenogenesis, during oogenesis first meiotic division does
not take place but second meiotic division occurs as usual. In this situation the ovum still remains
diploid. These ova, when reproduce parthenogenetically give rise to diploid off springs. For
example, Trichoniscus, Daphnia, Daphnia pulex etc.
(B) Meiotic thelytoky - If the eggs are formed by normal oogenesis process, but by one or other
reasons the eggs retain their diploid chromosomal number, then the parthenogenesis is called
meiotic thelytoky. It may happen because of autofertilization. Some species of order – Lepidoptera
exhibit this type of parthenogenesis.
- In some animals parthenogenesis alternates with normal sexual reproductive cycle. This is called
cyclic parthenogenesis e.g., Honey bee.
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(b) Artificial parthenogenesis : -
This type of parthenogenesis is done by artificial methods. Artificial parthenogenesis is done by putting
eggs in different atmospheres or by giving special stimulus to the eggs. Different artificial methods used
for this purpose are as follows -
(1) If we place eggs in brine or salt solution, KCl solution. Then eggs show parthenogenesis e.g. eggs of
sea-urchins.
(2) By short exposure of radiations on eggs or exposure of silk insect egg to sunlight.
(3) If eggs are given shocks of temperature.
(4) If eggs are pierced by needle dipped in the blood of same animal. The eggs of frog show
parthenogenesis by this method.
CLEAVAGE
producing a multicellular structure without changing its size. All these mitotic cells divisions
collectively called cleavage or segmentation. Due to the process of cleavage, a single celled zygote,
through a successive mitotic cell divisions changes into a complex multicellular structure. Cells
produced as a result of cleavage are termed as blastomeres. The total size of the embryo remains the
same. Though the number of blastomeres as a result of mitotic cell divisions increases, the size of
blastomeres gradually decreases are compared to parent cell. Interphase stage is very short in
cleavage. In interphase only DNA duplication and histone protein synthesis takes place up to some
extent. In the interphase of cleavage only 'S' phase is present, G1 & G2 phases are absent. Protein
synthesis and RNA synthesis do not occur during this interphase. Nucleolus is absent in the nucleus
of blastomeres. Size of blastomeres decreases during cleavage. When size of blastomere becomes
equal to that of size of somatic ells, the divisions of cleavage are stopped. Only normal cell division
take place. Cleavage can be observed till onset of gastrula stage. After gastrulation, cleavage is
completely checked. Nucleous appears first in gastrula stage. The consumption of oxygen is
increased during cleavage.
CLEAVAGE PLANE :
The traveling path of cleavage furrow in fertilized egg is called cleavage plane. Different animal eggs
show different cleavage planes : -
Vertical Plane
Meridianal Plane
Equatorial Plane
Transverse Plane
Vegetal Pole Vegetal Pole (V P)
[Cleavage Plane]
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PATTERNS OF CLEAVAGE :
(a) Radial Cleavage - In this pattern, cleavage furrows are straight and form right angle with each other. In
this case I, II cleavages are meridianal, which are at right angle to each other. III cleavage is equatorial
In this way 8-celled octate is formed. In radial cleavage, 4 blastomeres of upper tier and 4 blastomers of
lower tier are on sampe plane i.e, Blastomeres are arrangement in radial symmetry in the beginning.
(b) Biradial Cleavage - In this pattern, first two cleavages are meridianal and at right angle to each other
all III cleavage is vertical. In 8-celled stage 4 blastomeres of central zone are bigger and 4 blastomeres
of peripheral region are smaller.
Examples : - In the eggs of Ctenophora.
(c) Bilateral Cleavage - In this patterhn, first two cleavages are meridianal in same plane and III Cleavage
is transverse. i.e., embryo shows bilateral symmetry in 8-celled stage. The blastomeres of one side are
smaller and blastomeres of other side are larger.
Examples : - In the eggs tunicata, cephalochordata, amphibian and amphioxus.
(d) Spiral Cleavage - The cleavage furrow passes obliquely. In this pattern 4 blastomeres of lower tier
rotate clockwise or anticlock wise. If this rotation is clockwise, then it is called dextral spiral cleavage
e.g. In Mollusca. If this rotation of lower tier blastomeres is anti-clockwise, then pattern is called
sinistral spiral cleavage, e.g. In helminthes and annelida.
CLASSIFICATION OF CLEAVAGE :
On the basis of fate of blastomeres : -
A. Determinate Cleavage - In this pattern of cleavage, the fate of blastomeres is fixed, determined i.e.
each blastomere forms a particular portion of embryo. If (by certain reason) any blastomere is damaged
or destroyed, then the part of embryo (which would have development from that blastomere) will be
absent e.g., Nematoda, Annelida, Mollusca and Some chordates like amphibian & ascidians.
B. Indeterminate Cleavage - In this type of cleavage, the fate of blastomeres is not definite. All the
blastomeres form all the parts of embryo. If some blastomeres are lost, no loss is observed in this embryo. If
in the early stages of cleavage, the embryo is cut into small pieces, then each piece of embryo will develop
into a complex embryo, and all the embryos are identical. So identical twins are monozygous. This is the
basis of embryo cloning.
CLASSIFICATION OF CLEAVAGE :
On the basis of amount of Yolk : -
A scientist named Balfour gave a law. According to him, rate of cleavage is inversely proportional to
amount of yolk present in the egg. The yolk present in egg, disturbs the rate of cleavage. The rate of
cleavage is slow in that part of egg, in which amount of yolk is more, and the rate of cleavage is faster in
the portion of egg in which yolk is in lesser amount. Mostly cleavage is of 2 types : -
A. Complete or holoblastic : - When cleavage furrow passes through the egg completely. As a result of
this the whole egg divides. Holoblastic cleavage is found in all the eggs except megalecithal eggs. The
whole egg divides into blastomeres. No part of egg remains undivided. It is of 2 types : -
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(a) Equal holoblastic cleavage - In those eggs, in which amount of yolk is less and it is distributed
evenly in the egg, cleavage occurs in whole egg, blastomeres (So formed) are of same size. All the
parts of egg show same rate of cleavoage.
Example : - It is found in microlecithal and isolecithal eggs.
(b) Unequal holoblastic cleavage - In those eggs in which amount of yolk is medium and it is
distributed unevenly in the egg. The blastomeres are bigger and less in number where the
concentration of yolk is higherin the egg. The part of egg which contains small amount of yolk,
blastomeres here formed are smaller and more in number. The bigger blastomeres are called
megamere and smaller blastomere are called micromeres.
Examples : - Unequal holoblastic cleavage is present in mesolecithal and telolecithal eggs and
human eggs.
B. Meroblastic cleavage - This cleavage is found in megalecithal eggs, in which amount of yolk is large.
Cleavage does not occur in that part of egg, where yolk is present cleavage occurs only Cytoplasmic part,
yolk remains undivided. Meroblastic cleavage is of 2 types on the basis of distribution of yolk in egg.
(a) Discoidal meroblastic cleavage - Cleavage occurs only in blastodisc of egg. This is mainly found
in megalecithal or polylecithal eggs, because in these eggs, cytoplasm is found in the form of a disc.
Examples : - Reptilian eggs and birds eggs.
(b) Superficial meroblastic cleavage – In insect egg, central cytoplasm shows free central division,
due to which so many nuclei are formed. All these nuclei migrates towards peripheral cytoplasm.
Cleavage occurs only in peripheral region. As a result of this, a superficial layer of blastomeres is
formed around the yolk. This type of cleavage is also called superficial meroblastic cleavage.
Example - In centrolecithal eggs.
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Significance of Cleavage -
1. There is no change in shape and size developing embryo till blastula stage comes. Till then it remains
just like undivided egg in shape.
HUMAN EMBRYOLOGY :
Fertilization -
Fig. (5)
Fertilization is the union of two opposite types of gametes, spermatozoa and ova. The semen is a
mixture of spermatozoa and accessory fluids. Once deposited with in the vagina, the spermatozoa
proceed on their journey into and through the uterus and on up into the oviducts. Although spermatozoa
can swim several millimeters each second, their trip through the uterus and to the oviducts requires on
increase in their motility.
On the first hand, ejaculation of semen in the vagina triggers motility of spermatozoa. This is aided
further by muscular contraction of the walls of the uterus and the oviducts. An additional increase in
sperm motility occurs due to activation of the sperm by the viscous liquid secreted from the secreted
cells of the epithelial lining of oviduct mucosa. This phenomenon of sperm activation in mammals is
known capacitation. It takes about 5-6 hours for capacitation.
Before fusion of a spermatozoan with the egg, the spermatozoa are to penetrate a few barriers, the egg
membranes, which cover the egg. The activated spermatozoa undergo acrosomal reaction and release
varies chemicals, like hyaluronidase that acts on the ground substances of follicle cells, corona
penetrating enzyme that dissolves corona radiata, and zona lysine which perforates the zona
pellucida. All these chemicals are contained in the acrosome, located at the tip of the sperm head, and
are collectively termed sperm lysins. An average human ejaculate of 3-4 ml of semen contains 80-100
million spermatozoa. Out of these, only one will succeed in entering the egg and fertilizing it.
Fertilisation of egg with only one spermatozoan is known as monospermy.
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While the ovarian follicle is growing, the oogonium within it undergoes maturation. The oogonium enlarges
to form a primary oocyte. The primary oocyte undergoes the first meiotic division to shed off the first polar
body and becomes a secondary oocyte (fig. 5.2A). At the time of ovulation, the second meiotic division is in
progress and a spindle has formed for separation of the second polar body (fig. 5.2B)
Zona pellucida
Male pronucleus
Secondary oocyte
Spindle of second
Meiotic division A 23 23
First polar body First polar body
Female pronucleus
A B
23 23 Each chromosome
B 23 23 Duplicates itself
At this stage the 'ovum' enters the infundibulum of the uterine tube and passes into the ampulla (fig. 5)
Fertilization of the ovum occurs in the ampulla of the uterine tube. One spermatozoon pierces the zona
pellucida and enters the ovum. In response to egg sperm binding two things happen (1) depolarization
of egg membrane (2) cortical reaction i.e. formation of fertilization membrane to prevent polyspermy.
(After one spermatozoon has entered the ovum other spermatozoa cannot enter it). After the entry of the
spermatozoon, the second polar body is extruded. The chromosomes of the ovum now assume the
shape of a nucleus called the female pronucleus. At the same time the head of the spermatozoon (which
it will be remembered is formed from the nucleus) separates from the middle piece and tail, and
transforms it self into the male pronucleus (Fig. 5.2 D).
The male and female pronculei meet, but they do not fuse to form one nucleus. Their nuclear
membranes disappear and their chromosomes become distinct. It will be recalled that each pronucleus
has 23 chromosomes so that the fertilized ovum now has 46 chromosomes in all (fig 5.3 A).
Each of these 46 chromosomes splits into two (fig. 5.3B). Meanwhile, a spindle has formed, and one
chromosome of each pair moves to each end of the spindle (as in mitosis). Leading to the formation of
two daughter cells fig. (5.3C). This is called the two-cell stage of the embryo. Note that stricktly
speaking there is no one-cell stage of the embryo (fig. 6A)
As cleavage proceeds the ovum comes to have 16 cells. It now looks like a mulberry and it called the
morula (fig. 6D). It is still surrounded by the zona pellucida. If we cut a section across the morula we
see that it consists of an inner cell mass that is iscompletely surrounded by an outer layer of cells,
(Compaction). The cells of the outer layer will later give rise to a structure called the trophoblast (fig.
7A). The inner cell mass gives rise to the embryo proper, where as the cells of the trophoblast help to
provide nutrition to the embryo.
Some fluid now passes into morula from the uterine cavity, and partially separates the cells of the inner
cell mass from those of the trophoblast (fig. 7B). As the quantity of fluid increases, the morula acquires
the shape of a cyst. The cells of the trophoblast become flattened and the inner cell mass comes to be
attached to the inner side of the trophoblast on one side only (fig. 7C). The morula has now become a
blastocyst. That side of the blastocyst to which the inner cell mass is attached is called the embryonic or
animal pole. While the opposite side is the vegetable or abembryonic pole.
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(a) (b)
(c)
Fig. 7
The trophoblast has the property of being able to stick to the uterine (or other) epithelium and its cells
have the capacity to eat up other cells. As the embryo travels down the uterine tube, and the upper most
part of the uterine cavity ; it is prevented from 'Sticking' to the epithelium by the zona pellucida.
FORMATION OF GERM LAYERS (GASTRULATION) :
As the blastocyst develops further, it gives rise not only to the tissues and organs of the embryo, but also
to a number of structures that support the embryo and help it to acquire nutrition. At a very early stage
in development, the embryo proper acquires the form of a three-layered disc. This is called embryonic
disc (also called embryonic area, embryonic shield, or germ disc) The three layes that constitute this
embryonic disc are.
(i) Endoderm (endo = inside)
(ii) Extoderm (ecto = outside)
(iii) Mesoderm (meso = in the middle)
These are the three germ layers. All the tissues of the body are derived from one or more of these layers.
We have seen that the blastocyst is a spherical cyst lined by flattened trophoblastic cells, and that inside
it there is a mass of cells, the inner cell mass, attached eccentrically to the trophoblast Further changes
are as follows
(a) Some cells of the inner cell mass differentiate (i.e. they become different from others) into flattened
cells, that come to line its free surface (fig. 8A). These are called hypoblast and constitute the endoderm,
which is thus the first germ layer to be formed.
(b) The remaining cell of the inner cell mass become columnar (fig. 8D). These are called are called epiblast and
form the second germ layer, the ectoderm. The embryo is now in the form of a disc having two layers.
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(c) A space appears between the ectoderm (below) and the trophoblast (above). This is the amniotic cavity
(fig. 8C), filled by amniotic fluid, or liquor animal. The roof of his cavity is formed by amniogenic cells
(cells of Rauber) derived from the trophoblast, while its floor is formed by the ectoderm.
(d) Flattened cells arising from the endoderm, spread and line the inside of the blastocystic cavity. In this
way, a cavity, lined on all sides by cells of endodermal origin, is formed. This cavity is called the
primary yolk sac (fig. 8D)
(e) The cells of the trophoblast give origin to a mass of cells called the extra-embryonic mesoderm (or
primary mesoderm). These cells come to lie between the trophoblast and the flattened endodermal cells
lining the yolk sac, thus separating them from each other. These cells also separate the wall of the
amniotic cavity from the trophoblast (fig. 9A).
This mesoderm is called extra-embryonic because it lies out side the embryonic disc. It does not give
rise to any tissues of the embryo itself.
Endoderm
Amniogenic cells
Trophoblast
Amniotic cavity
Cavity of blastocyst
Cavity of blastocyst
Fig. 8
(f) Small cavities appear in the extra-embryonic mesoderm. Gradually these join together to from larger spaces
and, ultimately, on large space is formed. This cavity is called the extra-embryonic coelom (fig. 9B), it will
be seen that the extra-embryonic coelom does not extend into that part of the extra-embryonic mesoderm
which attaches the wall of the amniotic cavity to the trophoblast. The development embryo, along with the
amniotic cavity and the yolk sac, is now suspended in the extra-embryonic coelom, and is attached to the
wall of the blastocyst (i.e. trophoblast) only by this unsplitted part of the extra-embryonic mesoderm. This
mesoderm forms a structure called the connecting stalk.
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Fig. 9
(g) Formation of chorion and amnion : At this stage, two very important membranes are formed. One is
formed by the parietal extra-embryonic mesoderm (on the inside) and the overlaying trophoblast
(on the outside) this is called the chorian (fig. 9B). The other is the amnion which is constituted by the
amniogenic cells forming the wall of the amniotic cavity (excluding the extodermal floor). These cells
are derived from the trophoblast. We have already seen that the amnion is covered by the unsplit extra-
embryonic mesoderm, and that the connecting stalk is attached to it.
(h) With the appearance of the extra-embryonic mesoderm, and later of the extra-embryonic coelom, the
yolk sac becomes much smaller than before and is now called the secondary yolk sac. This alteration in
size is accompanied by a change in the nature of the lining cells. They are no longer flattended but
become cubical (fig. 9B).
(i) At this stage, the embryo proper is a circular disc composed of two layers of cells : the upper layer
(towards amniotic cavity) is the ectoderm, the cells of which are columnar, while the lower layer
(towards yolk sac) is the endoderm, made up of cubical cells (fig. 10)
Eead end
Cubical endodermA
Prochordal plate
Fig.10
(j) At one circular area a near the margin of the disc, the cubical cells of the endoderm become columnar.
This area is called the prochordal plate. The appearance of the prochordal plate determines the central
axis of the embryo (i.e. enables us to divide it into right and left halves), and also enables us to
distinguish its head and tail ends (fig. 10)
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(k) Soon after the formation of the prochordal plate some of the ectodermal cells lying along the central
axis, near the tail end of the disc, begin to proliferate, and form an elevation that bulges into the
amniotic cavity. This elevation is called the primitive streak (fig. 11). The primitive streak is at first a
rounded or oval swelling primitive streak later forms the Henson's node.
Ectoderm
Mesoderm
Endoderm
Fig. 11
(i) The cells that proliferate in the region of the primitive streak pass sideways, pushing themselves
between the ectoderm and endoderm (fig. 11). These cells from the intra-embryonic mesoderm (or
secondary mesoderm) which is the third germ layer.
Notochord
The notochord is a midline structure, that develops from mesoderm in dorsal region.
The notochord is present in all animals that belong to the phylum Chordata. In some of them e.g.
Amphioxus, it persists into adult life and forms the central axis of the body. In others, including man, it
appears in the embryo but only small remainants of it remain in the adult. Notochord elongates
considerably, and lies in the midine, in the position to be position to be later occupied by the vertebral
column. However, the notochord does not give rise to the vertebral column.
Neurulation : i.e formation of neural tube. After neurulation there occur three type of ectoderm.
(i) Somatic ectoderm (ii) Neural tube ectoderm (iii) Neural crest ectoderm.
Anterior part of neural tube differentiate brain and rest of the neural tube differentiate in spinal cord so
central nervous system is formed by neural tube.
TERATOGENY :
During the first 3 months of pregnancy the basic structure of baby is formed. This involves cell division,
cell migration, and differentiation of cells into the many types found in the body. During this period, the
developing baby called foetus is very sensitive to anything that interferes with developmental steps. Eg.
Virus infection of mother by rubella (German measles) virus or exposure to certain chemicals may cause
malformation in the developing embryo. Such agents are called teratogens (Monster Forming agents).
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GGENRAL STAGES OF EMBRYONIC DEVELOPMENTT
1. Morula - As a result of segmentation or cleavage activities, unicellular zygote changes into a solid ball
like multicellular structure. In the later stage of cleavage, clusters of sticky, cohering, protruding
(otuside) blastomeres are produced, which look like mulberry. This stage is termed as morula stage.
2. Blastulation - Cleavage continues in solid ball like morula and new formed blastomeres start
rearranging themselves. Cell-aggregation starts in blastomeres, due to the movement of these
blastomeres a cavity appears in the embryo, it is called as blastocoel. This cavity is schizogenous cavity
in origin i.e. it is formed by the separation of cells. Cell aggregation is also known as cohesion.
Blastomeres arrange themselves in the form of a layer around the blastocoel, this layer is termed as
blastoderm. The embryonic stage is now called blastula, and its formative activites is called blastulation.
Types of blastula
The shape of blastula depends on so many factors e.g. size of eggs, amount of yolk, distribution of yolk
in the eggs, frequency of cleavage and number of cleavage divisions. According to these factors, we can
classify blastula of different animals in different categories.
(a) Coeloblastula (b) Stereoblastula (c) discoblastula
(d) Blastocyst (e) Superficial blastula or Periblastula
(a) Coeloblastula - Blastocoel is wide and clear in this blastulation, it is completely surrounded by blastomeres
on all the sides i.e, blastocoel cavity is situated totally inside the embryo. Blastomeres are very small in size
as compared to blastocoel.
Blastocoel
[Periblastula]
[Blastocyst]
Blastula - of mammals is called blastocyst. In blastocyst all the embryonal cells occur in the form of solid
mass called embryonal knob. Embryonal knob (inner cell mass) is covered by protective layer called
trophoblast and it's cell just above the embryonal knob are trophoblast called cells of Rauber (amniogenic
cells). There occurs a cavity in between embryonal knob and trophoblast called albumin cavity. It is filled
with nutritive fluid absorbed from the wall of uterus. So albumin cavity is also nutritive-cavity.
SPECIAL POINT :
1. The growth phase is the longest phase during male gametogenesis. But in human oogenesis, maturation
phase is longest.
10. Although normal number of sperm are present in semen but if these are completely non motile. The
condition is known as necrospermia.
12. Due to high mortality rate in lower animals, the production of egg is more.
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14. Cat and rabbit both are induced ovulator.
15. The life span of eggs in female reproductive organs in human being is 48 hrs.
17. At the age of 45-50 yrs. In female the ovulation process will stop which is known as menopause.
18. The spermiation (release of sperms from sertoli cells) in all sertoli cells occurs simultaneously.
2. Mucosal membrane of lips, cheek gums, basal portion of mouth, some part of palate, nasal apertures.
4. Glans penis.
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5. Labia majora and outer part of labia minora.
6. Anterior epithelium of cornea, epithelium of conjunctiva, ciliary body and iris of eyes.
8. Glands :
(i) Exocrine –
(ii) Endocrine –
Derivatives of mesoderm
1. Connective tissues, superficial and deep fascia, ligaments, tendons, dermis of skin. (from dermatome)
2. Specialized connective tissues like adipose tissue, reticular tissues, bones, cartilages.
3. Teeth.
4. All muscles.
6. Kidneys, ureters, urinary bladder, posterior urethra of female, upper glandular part of prostate.
10. Joints.
11. Cornea, sclera, choroid ciliary body and iris related material.
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Derivatives of endoderm
1. Epithelial part of mouth, some part of palate, tongue, tonsils, pharynx, oesophagus, stomach, small
and large intestine, upper part of anal canal.
3. Respiratotry tract.
5. Major protion of urinary bladder, complete urethra of female except posterior part, complete urethra
of male except anterior and posterior part.
7. Glands :
(i) Exocrine –
(ii) Endocrine –
In addition to the above, the glands of gastrointestinal tract, major part of prostate etc. are also formed
by endoderm.
IImplantationn
The attachment of developing embryo to the appropriate body layer or surface to obtain nutrition is
called implantation. This phenomenon is a common event in most mammals (except prototheria) in
which embryo (blastocyst stage) after reaching in uterus attaches itself with the wall of the uterus. In
other animals like fishes, reptiles, birds, prototherian mammals etc., this nutritive connection is
established with the yolk present in egg. In higher mammals including men, the blastocyst on its contact
with endometrium of uterus gets completely buried in the wall of the uterus.
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ZONA PELLUCIDA
UTERUS
BLASTOCYST
FERTILIZATION
OVUM
INITIAL STAGE
OF
IMPLANTATION
Initially the oocyte after its release from ovary, comes into fallopian tube where the process of
fertilization is completed, Just after fertilization, embryonic development starts and a blastocyst is
formed after cleavage and morulation. In human being, the blastocyst gets attached with the uterine
endomdetrium in about four days after entering in uterus. At the same time, the cells of endometrium of
implantation area separate out and adhere with embryonic cells with the help of certain enzymes
secreted by the cells of trophoblast. In human, the site of implantation is generally mid-dorsal or mid-
ventral part of uterus. Implantation of blastocyst takes about 7-8 days after fertilization in human and by
12th day it is completely buried in the wall of the uterus. The place of entry through which the embryo
enters into the wall, is completely closed by a fibrous and cellular plug, known as closing coagulum.
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Types of Implantation
On the basis of the position of attachment in the uterus, implantation is of three types -
1. Central or Superficial implantation - In this type the blastocyst attaches superficially with the wall of
uterus, and remains suspended in the lumen of the uterus. This type of implantation occurs in lower
chordates, e.g. cow, pig, dog etc.
2. Interstitial implantation – The blastocyst is buries deeply inside the wall of uterus and covered by
endometrial tissues lying under epithelium. This type of implantation occurs in human being.
3. Eccentric implantation – It occur in rat, squirrel etc. In this type of implantation , the blastocyst settles
in the flods of epithelium of uterus. After some time it is completely surrounded by these folds.
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7 Weeks – Jaws, fingers and external ears begin to appear. The CR length (crown-rump length;
the length from head to the bottom of hips) is 19-20 mm.
8 Weeks – The embryo is completely surrounded by amnion, fingers and toes clearly visible,
almost all organs formed with continuing development, at the end of 8 th week the
embryo appears like a little human, now called as foetus; C-R length is 28 to 30 mm.
5 months – Blood formation starts in bone marrow Decidua capsularis and parietalis connect
together, hairs appear.
7 WEEK EMBRYO
8 WEEK FOETUS
9 WEEK FOETUS
10 WEEK FOETUS
9 months – placenta attains maximum size, nails on fingers appear. In the next 10 days the foetus
is ready to born as a little bady.
The above mentioned timing are approximate time periods. Some times, due to some reasons, certain babies
are born before stipulated time. The babies born in 7th month may also survive as normal babies.
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EXTRA EMBRYONIC MEMBRANES AND PLACENTA
83
1. Amnion - It is formed by the layer of amniogenic cells present around the amniotic cavity and the extra
embryonic mesoderm. Extra embryonic mesoderm layer surrounds the amnion. The connecting stalk is
also attached with it. With a gradual increase in size the amnion covers the embryo from all sides. After
about eight weeks of fertilization, amnion is completely incorporated into connecting stalk, which finally
forms the umbilical cord. Embryo, in this stage, is called as foetus remains hanging in amniotic fluid.
2. Chorion - It is formed by the extra embryonic parietal layer of mesoderm and the cell of trophoblast.
After implantation of blastocyst, the trophoblast gives out several figner like processes, the chorionic
villi which get embedded into uterine endometrium Mesoderm also contributes in the formation of these
villi. After a period of four these villi disappear from all parts except the connecting stalk where they
grow rapidly and participate in the formation of placenta.
3. Yolk sac - Yolk sac is formed by the cells of extra embryonic visceral mesoderm and endoderm.
Initially the sie of yolk sac is larger as compared to that of the embryo. About eight weeks after
fertilization, the yolk is reduced in size and changes into a tubular structure. Ultimately a placenta is
developed with the incorporation of yolk sac and mesodermal connecting stalk with the amnion and
chorion.
4. Allantois - It is a solid and cylindrical mass formed by embryonic mesoderm. A small cavity lined
by endodermal cells develops in it. The mesoderm of allantois forms many small blood vessels in
this region. These vessels connect the embryo with placenta and ensure nutritional and respiratory
supply to embryo. In human, allantois does not function to store the excretory wastes as it does in
reptiles and birds.
PLACENTA
The eggs of viviparous animals are unable to develop into their embryos outside the uterus
independently. This is because of the very little or negligible amount of yolk present in these eggs,
which can not fulfill the nutritional and other physiological demands of a developing embryo. Here the
embryo depends upon maternal tissues for shelter, nutrition, respiration etc. These animals therefore,
have developed adaptation, respiratory and other physiological requirements from mother's body.
Structure of Placenta
Placenta is not a simple membrane. It is made up of the tissues from two different sources –
Maternal tissue - These include uterine epithelium, connective tissues and blood capillaries.
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Embryonic tissue - These include extra embryonic membranes (mainly chorion). Yolk sac and allantois
may also take part in placenta formation. Embryonic connective tissues and blood capillaries are also
constituents of it.
1. Yolk sac placenta - It is formed by yolk sac and uterine epithelium. For example, Elasmobrancs
(Sharks), Mustelus etc.
2. Choria-vitelline placenta - It is formed by chorion and yolk sac combinely. Hence it is called as
choriovitelline placenta. For example, Didelphis, Macropus and other metatherian mammals.
3. Chorio-allantoic placenta - This type of placenta is formed by embryonic chorion and allantoic
membranes. It is also referred to as a true placenta. It is found in eutherian mammals.
1. In this type of placenta, allantoic mesodern and the mesoderm of umbilical cord jointly form the blood
vessels of umbilical cord. The endodermal part of the allantois remains as a very small cavity.
2. To obtain nutrition from maternal blood several finger like processes or villi are formed by chorion
which penetrate deeply into the crypts of uterus. Initially the villi are scattered over the whole surface of
chorion but later they become restricted in the deciduas besalis region. The chorionic villi on the
remaining surface disappear shortly. The part of chorion, which helps in placenta formation is known as
chorionic frondosum.
DECIDUA BASALIS
DECIDUA BASALIS
DECIDUA BASALIS
CHORIONIC VILLI DECIDUA BASALIS
CHORION
DECIDUA CAPSULARIS
DECIDUA
UTERINE LUMEN CAPSULARIS
DECIDUA
CHORIONFRONDOSUM PARIETALIS
UTERINE LUMEN
CHORION
Subdivisions of decidua
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Classification of Placenta
On the basis of different characters, the placenta are classified in following manner –
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deciduas, where placenta is formed is called deciduas basalis whereas, the part separating the embryo
from lumen of uterus is called deciduas capsularis. The remaining part of lumen of uterus is called
deciduas parietalis. Decidua also comes out from uterus at the time of parturition. On the basis of
intimacy between embryo and uterine wall the placenta is classified into three classes –
(i) Non-deciduate or Semi placenta - In this type of placenta, there is no close and rigid association
between embryo and the wall of uterus. Hence, at the time of parturition, there is no bleeding as the
chorionic villi are easily pulled out from the crypts of uterus. For example, cow, buffalo, horse, pig.
(ii) Contra-deciduate placenta - There is a close association between embryonic and maternal tissues.
However at parturition, the damaged maternal and embryonic tissues along with the part of placenta
remain inside the uterus which are absorbed is situ by leucocytes. For example – Parameles, Talpa etc.
(iii) Deciduate placenta - This type of placenta is found in human, dog, hare etc. It is characterized with a
very close association between chorionic villi and uterine wall. At the time of birth, the mucosal
covering of the uterus is also damaged and discarded outside. This results in an extensive bleeding at
child birth. This placenta is known as a true placenta.
2. On the basis of implantation
(i) Superficial - When the placenta is situated in the lumen of uterus. For example, Parameles, pig, cow,
cat etc.
(ii) Eccentric - The placenta is situated in the fold or pocket of the cavity of uterus. For example - rat,
squirrel etc.
(iii) Interstitial – This type of placenta is found in man, guinea pig, apes etc. The chorionic sac (placenta)
penetrates deep inside the wall of uterus. Hence, the association between embryo and maternal part
becomes very close.
(ii) Cotyledonary placenta – The villi are distributed in small isolated groups on the chorionic surface.
These groups of villi are called as cotyledons. For example, cow, buffalo, sheep, deer etc.
(iii) Zonary placenta - This type of placenta have the villi distributed in a belt shaped zone which is large
sized and circular.
Zonary placenta is of two types –
(a) Complete zonary placenta - The belt of villi is complete and ring shaped in it. For example -
dog, cat, lion etc.
(b) Incomplete Zonary placenta - The belt of villi is incomplete in it. For example - raccoon.
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(iv) Discoidal placenta - In this type of placenta, whole of the chorionic surface is covered by villi in initial
stage, but the villi disappear later from later from most area except the region of implantation, that is
only a disc like region is left with villi. Discoidal placenta is also of two types –
(a) Mono discoidal placenta - The villi are present only on dorsal surface in single circular disc like
area. For example – human, hare etc.
(b) Bi discoidal placenta - If the villi are distributed in two disc like areas, the placenta is called as
bidiscoidal, eg. Monkeys.
The blood of maternal and embryonic do not mix together through placenta. The blood circulations of
the two sides are kept separated by one or more layers described below –
1. Maternal endothelium
2. Uterine connective tissue Maternal layes
3. Uterine epithelium
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4. Trophoblast/Chorion
5. Chorionic connective tissue Foetal layes
6. Endothelium of embryonic blood vessels
The transportation of various materials takes place by diffusion through these six layers the intimacy
between maternal and embryonic tissues in different mammals is determined by the presence or absence
of these layers in placenta. Therefore, on the basis of presence or absence of the above layers, the
placenta is of five types.
1. Epitheliochorial - It is the most primitive type of placenta in which all the six layers. mentioned
earlier, remain intact. For example pig, horse etc.
2. Syndesmochorial - In this type of placenta the uterine epithelium is eroded by chorionic villi, so only
two maternal layers remain functional. Therefore, along with three foetal layers, total five layers are
preent in this placenta. For example - sheep, goat, cow etc.
3. Endotheliochorial - Here uterine connective tissue layer is also damaged along with uterine epithelium
layer. Therefore only four layers (3 foetal and one maternal) are found in this placenta eg. dog, cat, etc.
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4. Haemochorial – All the three maternal layers are penetrated in this placenta. The chorionic epithelium
comes in direct contact with uterine blood sinusoids. For example – man, monkey, bat etc.
The placenta of human mainly secretes two steroid hormones like estradiol and progesterone, and two
protein hormones like human chorional gonadotropin HCG and human placental somatomammotropin
HCS large amount of –HCG, hormone is secreted, during early pregnancy, from the placenta. Because of
this reason its quantity increases in the urine of pregnant lady. On the basis of this fact, pregnancy test is
performed. The above hormones are also held responsible for keeping the corpus luteum active, protection of
embryo, prevention of abortion and growth of mammary glands.
Functions of placenta
3. The small molecules like O2, CO2, H2O etc. and other inorganic substances like chlorides, phosphates,
sodium, potassium, magnesium etc. are also diffused through placenta.
4. Large molecules like lipids, polysaccharides, carbohydrates proteins etc. are obtained by pinocytosis
process.
5. The nutritional substances are supplied to embryo from the mother through placenta.
6. Placenta also serves as a respiratory medium for exchange of O2 and CO2 between embryo and mother.
7. The nitrogenous and metabolic wastes from foetus are released into the blood of mother by diffusion
through placenta.
8. The antibodies for measles, chickenpox, polio etc. present in the blood of mother reach the embryo
through placenta.
10. If a female takes some harmful chemicals, liquor, drugs etc. during pregnancy, these may cross the
placenta and on reaching into foetus may cause deformity during organogenesis. (eg. Thallidomide)
11. Placenta itself secretes some hormones like progesterone, estrogen, lactogen, HCG, HCS etc.
12. Progesterone, maintains and supports the foetus during the whole pregnancy period. At the time of
parturition, relaxin is secreted by placenta which lubricates and widens the birth canal to facilitate child
birth.
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REPRODUCTIVE HEALTH
Methods of contraception
An ideal contraceptive should be user-friendly, easily available, effective and reversible with no or least
side-effects. It also should in no way interfere with the sexual drive, desire and/or the sexual act of the
user. A wide range of contraceptive methods are presently available which could be broadly grouped
into the following categories, namely Natural/Traditional, Barrier, IUDs, Oral contraceptives,
Injectables, Implants and Surgical methods.
(1) Natural methods :
work on the principle of avoiding chances of ovum and sperms meeting. Periodic abstinence is one
such method in which the couples avoid or abstain from coitus from day 10 to 17 of the menstrual cycle
when ovulation could be expected. As chances of fertilisation are very high during this period, it is
called the fertile period. Therefore, by abstaining from coitus during this period, conception could be
prevented.
Withdrawal or coitus interruptus is another method in which the male partner withdraws his penis
from the vagina just before ejaculation so as to avoid insemination.
Lactational amenorrhea (absence of menstruation) method is based on the fact that ovulation and
therefore the cycle do not occur during the period of intense lactation following parturition. Therefore,
as long as the mother breast-feeds the child fully, chances of conception are almost nil. However, this
method has been reported to be effective only upto a maximum period of six months following
parturition. As no medicines or devices are used in these methods, side effects are almost nil. Chances
of failure, though, of this method are also high.
(2) Barrier Methods :-
In barrier methods, ovum and sperms are prevented
from physically meeting with the help of barriers. Such
methods are available for both males and females.
Condoms are barriers made of thin rubber/latex sheath Condom for male
that are used to cover the penis in the male or vagina
and cervix in the female, just before coitus so that the
ejaculated semen would not enter into the female
reproductive tract. This can prevent conception.
‘Nirodh’ is a popular brand of condom for the male.
Use of condoms has increased in recent years due to its
additional benefit of protecting the user from
contracting STDs and AIDS. Both the male and the Condom for female
female condoms are disposable, can be self-inserted and
thereby gives privacy to the user.
Diaphragms, cervical caps and vaults are also barriers
made of rubber that are inserted into the female reproductive tract to cover the cervix during coitus.
They prevent conception by blocking the entry of sperms through the cervix. They are reusable.
Spermicidal creams, jellies and foams are usually used alongwith these barriers to increase their
contraceptive efficiency.
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(3) Intra Uterine Devices (IUDs) :
These devices are inserted by doctors or expert nurses in
the uterus through vagina. These Intra Uterine Devices
are presently available as the non-medicated IUDs (e.g.,
Lippes loop), copper releasing IUDs (CuT, Cu7,
Multiload 375) and the hormone releasing IUDs
(Progestasert, LNG-20).
IUDs increase phagocytosis of sperms within the uterus
and the Cu ions released suppress sperm motility and the
fertilising capacity of sperms.
The hormone releasing IUDs, in addition, make the
uterus unsuitable for implantation and the cervix hostile
to the sperms.
IUDs are ideal contraceptives for the females who want Copper T (CuT)
to delay pregnancy and/or space children. It is one of
most widely accepted methods of contraception in India.
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(5) Surgical methods :
Also called sterilisation, are generally advised for the male/female partner as a terminal method to
prevent any more pregnancies. Surgical intervention blocks gamete transport and thereby prevent
conception. Sterilisation procedure in the male is called ‘vasectomy’ and that in the female,
‘tubectomy’.
In vasectomy, a small part of the vas deferens is removed or tied up through a small incision on the scrotum
whereas in tubectomy, a small part of the fallopian tube is removed or tied up through a small incision in the
abdomen or through vagina. These techniques are highly effective but their reversibility is very poor.
Vasectomy Tubectomy
Infertility
A large number of couples all over the world including India are infertile, i.e., they are unable to
produce children inspite of unprotected sexual co-habitation. The reasons for this could be many–
physical, congenital, diseases, drugs, immunological or even psychological. In India, often the female is
blamed for the couple being childless, but more often than not, the problem lies in the male partner.
Specialised health care units (infertility clinics, etc.) could help in diagnosis and corrective treatment of
some of these disorders and enable these couples to have children. However, where such corrections are
not possible, the couples could be assisted to have children through certain special techniques
commonly known as assisted reproductive technologies (ART).
In majority of animals, as a result of sexual reproduction the structure formed is termed as the zygote
and it gives rise to complete animal. This is termed as ''embryogenesis'' and the animals, so formed are
termed as oozoids. They have the most advanced characters.
HISTORY :
(1) Aristotle is known as ''Father of Embryology'' he first studied the development in chick and other
embryos. He gave its description in his book ''Historia Animalia''.
(2) Leeuvenhock (1671) - He observed and described human sperm for the first time.
- According to Hartsoeker and Leeuvenhock there is a small model of developing animals present in the
head of the sperm of that animal. This small model is called homunculus. Both these scientists are
called spermists, and this theory is called '' Theory of spermist ''.
(3) Swammer Dame, Haller, Bonette & Malpighi : - According to these scientists, small model of animal
is always present in the egg. These scientists are called Ovists, and their theory is known as 'Ovists
theory'
(4) Schleiden & Schwann : - Both the scientists established the cellular structure of egg and sperm.
(5) Pander : - He described the presence of three germinal layers in chick embryo.
(6) Fredrich Wolff : - He first presented the ''theory of epigenesis''.
(7) Muller : - He gave the recapitulation theory.
(8) Haeckel : - He gave the details of Recapitulation theory and named it as the bio-genetic law.
- Bio-genetic Law : - According to this each organism during its embryonal development, passes
through all stages, through which its species has evolved or embryo repeats its ancestry. i.e. Ontogeny
recapitulates its Phylogeny.
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(9) ''Carl Ernest Von Baer'' : - He is known as the ''father of modern embryology.'' He gave the Baer's
Law which in turn proves the recapitulation theory.
According to this law, during embryonal development, the development of general structures takes
place earlier and specific structures develop at last or later on.
(10) A. Weismann : - He gave the theory of germplasm or the theory of continuity of germplasm.
According to him, there are 2 types of protoplasm in the body of animals : -
(i) Somatoplasm (ii) Germplasm
Somatoplasm dies but the germplasm is never destroyed, rather it is transferred to the progenies.
(11) Wilhelim : - He studied embryonal development in frog and gave the mosaic theory.
- He said that there are some presumptive areas in the eggs of frog. These areas form specific structures
during embryonal development. This is termed as ''Promorphology .'' and these type of eggs are termed
as the mosaic eggs.
(12) Hand Driesch : - He studied embryonal development is sea-urchin and gave the regulative theory.
- In the eggs of Sea-Urchin presumptive areas are not found i.e. promorphology is not found. So, each
part of the egg is capable of forming the complete embryo. These type of eggs are termed as regulative
eggs.
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