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Neurulation

Neurulation is the formation of the vertebrate nervous system in embryos. The notochord induces the formation of the CNS by signaling the ectoderm above it to form the thick and flat neural plate. The neural plate then folds in on itself to form the neural tube, which will then later differentiate into the spinal cord and brain.

Neurulation (contd)
Different portions of the neural tube then form by 2 different processes in different species: 1. Primary Neurulation the neural plate creases inward until the edges come into contact and then fuse. 2. Secondary Neurulation the tube forms by hollowing out of the interior of a solid precursor

24-hr Chick

22-23 days of Human

23-26 days of Human

Formation of the Neural Tube


Secondary Neurulation 1. Occurs beyond the caudal neuropore 2. lumbar and tail region 3. Exclusive mechanism for fish 4. Starts with formation of medullary cord 5. Cavitation of cord to form hollow tube

Secondary Neurulation

Differentiation of Neural Tube


Major morphological changes: differentiation of brain vesicles and spinal cord Differentiation of neural tube cells Development of peripheral nervous system

Differentiation of Brain Vesicles


Anterior neural tube bulges: 3 primary vesicles:

Then further differentiation into 5 secondary


vesicles:

Differentiation of the Neural Tube


Neural tube must maintain dorsal-ventral polarity
Sensory neurons- dorsal Motor neurons- ventral

Accomplished by inductive cascades


Dorsal: BMPs from epidermisRoof plate cells in neural tubeTGF-B cascadeCell differentiation Ventral: Sonic hedgehog from notochord and retinoic acid from somitesFloor plate cells of neural tubeshh gradientCell differentiation

Differentiation of the Neural Tube


Histological changes 1. Neural tube initially a single layer of cells: germinal epithelium 2. Cells are called neural stem cells
Neurons Glial Cells: Myelin sheath

Glial Guidance

Development of Peripheral Nervous System Divisions:


Autonomic NS
Sympathetic vs. Parasympathetic

Somatic NS

Anatomy
Sensory Neurons
Enter dorsal part of spinal cord Soma located outside of cordDorsal ganglia Form Dorsal Root of Spinal Nerve

Motor Neurons
Soma in ventral gray matter Somatic NS: Neurons run directly from SC to muscle Autonomic: 2 Neurons
Sympathetic: Ganglia near SC Parasympathetic: Ganglia near or in or near organ

Development of Peripheral Nervous System


Anatomy Spinal Nerves:Spinal Cord Sensory fibers of somatic nervous system: Dorsal root Preganglionic neurons of sympathetic system: Ventral root Motor fibers of somatic nervous system: Ventral root Cranial Nerves: Brain stem Sensory fibers of somatic nervous system: Dorsal root Preganglionic neurons of parasympathetic system: Ventral root Motor fibers of somatic nervous system: Ventral root

Origin of PNS Cells


From neural tube:
All motor neurons of somatic nervous system Preganglionic neurons of autonomic system

From neural crest:


Sensory nerves and associated ganglia Postganglionic neurons of autonomic system

Neural Crest Cells


Induced by organizing cells of notochord Main functional groups:
Cranial neural crest: Bones and connective tissue of face Tooth primordia Thymus, parathyroid, thyroid glands Sensory cranial neurons Parasympathetic ganglia and nerves Parts of the heart (cardiac neural crest)

Neural Crest Cells


A group of cells, which breaks away from the closing neural tube and populate the periphery (as opposed to the CNS, which will develop from the tube). Neural crest will supply all neurons of the PNS and a variety of other peripheral structures, ranging from melanocytes to craniofacial bones to cells of the adrenals. This population of cells separates from the neural plate shortly after the fusion of the neural folds, and streams of dividing cells begin their journey through the embryo. The expression of which genes are turned off during this migratory stage? And, this occurs for individual cells as well as for groups of cells

Neural Crest Cells

For neural crest cells, migratory pathway is particularly important in cellular determination, as location (or path) controls the availability of inducing factors for particular cell fates. Making Cells The use of chimeras has been invaluable in the study of individual cell fates. What is a chimera? Cells with a different genome; e.g., chick/quail mix heterochromatin marker not found in chick. [3H] thymidine labeling has helped in the delineation of migratory pathways and development potential of neural crest cells.

Neural Crest Cells

Interaction: Neural crest migration/movement is rigid and occurs in a ventral (1st cells give rise to ventral structures) - todorsal order in the head. Migratory pathways are linked to neuronal fate. What is the mostly likely result of transplant experiments when early cells will switch their fate? Extrinsic cues ? Whether these come from the pathway itself or the final destination (target-derived cues) is not clear. As in the CNS, the earlier the cell is, the more pleuripotent it is (the more flexibility of fate).

Neural Crest Cells


Main functional groups: The stream of neural crest cells migrates via a ventral route to form:
Trunk neural crest: Melanocytes (via the dorsal route) Sensory neurons (DRG) Sympathetic ganglia and nerves (ANS) Medulla of adrenal glands (chromaffin cells) Note that they migrate segmentally (sclerotome) only in the rostral compartment.

Neural Crest Cells


Migration:
Epithelial to mesenchyme transition Migrational pathways are established by juxtacrine signals: Fibronection, laminin in ECM + integrins Ephrin proteins: Restrict movement Contact inhibition Use of existing structures Migration ceases when these signals are reversed

Migration of Neural Crest Cells


Unlike cells in the CNS, which migrate radially along glial fibers, neural crest cells crawl along independently (like fibroblasts). Motility is promoted by integrins bind cell surface to ECM (how does this contrast with cadherins?) Prominent ECM components along neural crest cell pathway: fibronectin, laminin, collagen. The ECM provides attractive (permissive) cues for movements, as well as a substrate on which to bind. A set of repulsive cues in neighboring structures keeps cells in their precise migratory pathway

Migration of Neural Crest Cells


As the cells reach their destination, the expression of cadherins is once again activated (had been repressed during free movement) cells aggregate into ganglia when they undergo terminal neuronal and glial differentiation. Side bar: retroviral labeling: A cell can be labelled permanently and heritably by injection with a retrovirus carrying a gene (e.g., galactosidase) incorporated into cells DNA and then expressed. A substance, which will turn blue from the action of the enzyme, can then be introduced in a histochemical test.

Neural Crest Cells


Differentiation:
Largely based on location along neural tube and their migration route:

Neural Crest Cells


Differentiation:
Migration routes along trunk: Ventral pathway: cells move through anterior portion of somite toward ventral side of embryo Cells become: sensory neurons, sympathetic ganglia, medulla of adrenal gland Dorsolateral pathway: cells move between epidermis and somite Cells become: melanocytes Basic organization of the PNS is established by the migratory pathways of the neural crest cells

Neural Crest Cells


Differentiation:
How do they know what to become? Most cells are pleuripotent- fate determined by position Paracrine factors play a role Example: Endothelin-3 and Wnt Some exceptions: only NC cells from head make bone Individual cells may differentiate early in migration

Differentiation of Neurons
Within nerve tube:
Dorsal Interneurons Ventral Motor neurons

Differentiation of Neurons
Motor neurons:
Tissues they innervate depends on: Anterior-posterior location along the nerve tube When the cells were born

Axonal Pathways

Spinal Cord 2. Sensory ganglia 3. Autonomic motor neurons

1. Motor neurons from ventral root

Axonal Pathways
Establishing pathways and connections:
Pathway selection Target selection Address selection

Axonal Pathways
1. Pathway Selection Pathway axon takes influenced by extracellular matrix and cells encountered: signals by both paracrine and juxtacrine factors:

Cell adhesion and contact guidance: Haptotaxis Growth cone repulsion


Ephrin and semaphorin proteins

Labeled Pathways Hypothesis: Pioneer Neurons Diffusible molecules

Axonal Pathways 2. Target Selection:


Neurotrophins on target cells (muscle or another neuron)

3. Address selection: constructing the synapse

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