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Learning Objectives
Describe the composition and functions of blood. Explain how red blood cells transport oxygen. Explain the basis of blood typing. Define hemostasis and distinguish it from homeostasis. homeostasis. Describe various blood disorders.
platelets
Fig. 8.1
Plasma further contains ions, glucose, amino acids, signaling molecules, and dissolved gases.
Components
1. Water 2. Plasma proteins (albumin, globulins, fibrinogen, etc.)
Relative Amounts
91%-92% of plasma volume 7%-8% 1%-2% Solvent
Functions
3. Ions, sugars, lipids, amino acids, hormones, vitamins, dissolved gasses 1. White blood cells: Neutrophils Lymphocytes Monocytes(macrophages)
Eosinophils Basophils
250,00-300,000
Fig. 8.1
They contain hemoglobin, an iron-containing protein ironthat binds with oxygen. They also carry a small amount of carbon dioxide.
Red blood cells originate from stem cells in the bone marrow.
neutrophils
mast cells
T lymphocytes
eosinophils
B lymphocytes
? stem cells in marrow red blood cells (erythrocytes) monocytes (immature phagocytes)
dendritic cells
macrophages
megakaryocytes
platelets
Fig. 8.2
Only a tiny amount of oxygen is dissolved in blood plasma. Most of the oxygen is bound to the heme groups of hemoglobin; oxygen-bearing hemoglobin is oxygenoxyhemoglobin. called oxyhemoglobin.
The amount of oxygen bound to hemoglobin changes as conditions in the tissues vary.
Binding of oxygen is favored by conditions in the lungs: abundant oxygen, cooler temperature, and neutral pH (in lungs). Release of oxygen is favored in the tissues where the oxygen levels are lower, temperatures higher, and pH more acidic. Hemoglobin also transports a small amount of carbon dioxide.
Each hemoglobin molecule has four polypeptide chains (globin proteins), each of which possesses a heme group containing an iron molecule; each iron binds one molecule of oxygen.
heme group
Hemoglobin
Four
polypeptide chains, two types: alpha and beta, each with heme group: iron molecule binds oxygen. Each hemoglobin molecule binds 4 oxygen molecules.
Red blood cells form from stem cells located in red bone marrow.
The hormone erythropoietin from the kidneys is the stimulus for stem cell division. Mature red blood cells have no nuclei and live for only about 120 days.
Macrophages remove old blood cells from the bloodstream; amino acids are returned to the blood, iron is returned to the bone marrow, and heme groups are converted to bilirubin. bilirubin. Red cell counts remain rather constant at 5.4 million/microliter million/microliter for males and 4.8 million for females.
Kidney
Erythropoietin
1 1
Reduced oxygen in blood Relieves 5
The kidneys detect reduced O2 in the blood. When less O2 is delivered to the kidneys, they secrete the hormone erythropoietin into the blood. Erythropoietin stimulates production of red blood cells in bone marrow. The additional circulating RBCs increase O2 carried in blood. The increased O2 relieves the initial stimulus that triggered erythropoietin secretion.
3
Developing red blood cells in red bone marrow
3 4 5
Fig. 8.4
All cells of the human body have surface proteins and other molecules that serve as self identification markers. Any protein marker that prompts a defensive action is antigen. called an antigen. The human body produces antibodies that recognize markers on foreign cells as nonself and stimulate nonself immune reactions.
The ABO group of blood types includes key self markers on red blood cells.
ABO blood groups are based on glycoprotein surface markers on red blood cells.
Type A has A markers; type B has B markers. Type AB has both markers; type O has neither marker.
Depending on ABO blood type, the body will also possess antibodies to other blood types; ABO blood typing is done to prevent incompatible blood types from being mixed.
Mixing incompatible blood types can cause the clumping called agglutination.
Type A blood types do not have antibodies against A markers, but they do have antibodies to type B; Type B blood types do not have type B antibodies, but they do have type A antibodies, etc.
A type A person cannot donate blood to a type B person because they are incompatible. incompatible. When mixed, markers on the surface of red blood cells (not just the ABO markers) that do not match will cause the blood cells to undergo agglutination, agglutination, a defense response where the blood cells clump.
Table 8.1
Table 8.2
Clumped cells can clog small blood vessels, damage tissues, and cause death.
Antigen A
Red blood cells usually burst Side effects disrupt kidney function
Clumping blocks blood flow in capillaries Oxygen and nutrient flow to cells and tissues is reduced
Fig. 8.5a
Rh Blood Typing
Rh Blood Typing
An Rh- mother who bears an Rh+ child can also become sensitized to the Rh antigen; secondary children may be at risk from maternal antibodies.
In hemolytic disease of the newborn, too many newborn, cells may be destroyed and the fetus dies. Medical treatment (RhoGam) given to the mother (RhoGam) after the birth of the first Rh+ baby can inactivate the Rh antibodies.
Rh Blood Typing
Blood flow
Prothrombin Damaged cells and platelets release substances that activate clotting factors Prothrombin activator Ca2+ Fibrinogen Thrombin Ca2+
Fig. 8.8
Clots that form in unbroken vessels can be lifelifethreatening as it blocks blood flow.
A clot that stays where it forms is called a thrombus (condition is thrombosis); one that breaks free and moves is called an embolus (condition is embolism). A stroke occurs when an embolus blocks flow to some part of the brain.
Hemophilia is a genetic disorder where clotting factors are absent from the blood so it does not clot properly.
Blood Disorders
In iron-deficiency anemia, red cells contain too little ironanemia, hemoglobin, usually resulting from an iron-poor diet. ironPernicious anemia is caused by a deficiency of folic acid or vitamin B12.
Aplastic anemia results from a destruction of the red bone marrow and its stem cells.
Blood Disorders
Hemolytic anemias are caused by the premature destruction of red blood cells.
Sickle cell anemia, a genetic anemia, disease, is one cause. Malaria is a major cause of hemolytic anemia and follows infection by a protozoan transmitted by mosquitoes. In thalassemia, individuals produce abnormal thalassemia, hemoglobin.
Figure 8.10
Blood Disorders
Blood Disorders
Fig. 8.11