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Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor.
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Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

Dec 24, 2015

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Page 1: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

Developmental Neuroscience

Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi-Montalcini)

Page 2: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

Embryonic and Fetal Development of the Human Brain

Actual Size

Actual Size

Page 3: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

Lateral view of the human brain shown at one-third size at several stages of fetal development. Note the gradual emergence of gyri and sulci.

Photographs of Human Fetal Brain Development

Page 4: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

Nervous System Development in the Human Embryo

(a) At 18 days after conception the embryo begins to implant in the uterine wall. It consists of 3 layers of cells: endoderm, mesoderm, and ectoderm. Thickening of the ectoderm leads to the development of the neural plate (inserts). (b) The neural groove begins to develop at 20 days.

Page 5: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

Nervous System Development in the Human Embryo

(c) At 22 days the neural groove closes along the length of the embryo making a tube. (d) A few days later 4 major divisions of the brain are observable – the telencephalon, diencephalon, mesencephalon, and rhombencephalon.

Page 6: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

Eight Phases in Embryonic and Fetal Development at a Cellular Level

1. Mitosis/Proliferation

2. Migration

3. Differentiation

4. Aggregation

5. Synaptogenesis

6. Neuron Death

7. Synapse Rearrangement

8. Myelination

8 stages are sequential for a given neuron, but all are occurring simultaneously throughout fetal development

Page 7: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

Eight Phases in Embryonic and Fetal Development at a Cellular Level

1. Mitosis 2. Migration 3. Aggregation and 4. Differentiation

5. Synaptogenesis 6. Death 7. Rearrangement

8. Myelination

Page 8: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

1. Mitosis/Proliferation

•Occurs in ventricular zone

•Rate can be 250,000/min

•After mitosis “daughter” cells become fixed post mitotic

Page 9: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

1. Mitosis/Proliferation: Neurons and Glia

At early stages, a stem cell generates neuroblasts. Later, it undergoes a specific asymmetric division (the “switch point”) at which it changes from making neurons to making glia

Page 10: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

2. Migration

Note that differentiation is going on as neurons migrate.

Page 11: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

2. Migration

Radial glial cells act as guide wires for the migration of neurons

Radial Glia

Page 12: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

2. MigrationGrowth Cones

Growth cones crawl forward as they elaborate the axons training behind them. Their extension is controlled by cues in their outside environment that ultimately direct them toward their appropriate targets.

The fine threadlike extensions shown in red and green are filopodia, which find adhesive surfaces and pull the growth cone and therefore the growing axon to the right.

Page 13: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

2. MigrationGrowth Cones

Scanning electron micrograph of a growth cone in culture. On a flat surface growth cones are very thin. They have numerous filopodia

Ramon y Cajal drew these growth cones showing their variable morphology

Page 14: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

2. Migration: How Do Neurons “Know” Where to Go?

There are extrinsic and intrinsic determinants of neurons’ fate.

A. Extrinsic signals

B. Different sources of extrinsic signals

C. Generic signal transduction pathway

D. Intrinsic determinants

Page 15: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

3. Differentiation

•Neurons become fixed post mitotic and specialized

•They develop processes (axons and dendrites)

•They develop NT-making ability

•They develop electrical conduction

Page 16: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

3. Differentiation

Development of the cerebral cortex

The ventricular zone (VZ) contains progenitors of neurons and glia. 1st neurons establish the preplate (PP); their axons an ingrowing axons from the thalamus establish the intermediate zone (IZ). Later generated neurons establish layers II-VI. After migration and differentiation there are 6 cortical layers.

Page 17: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

4. Aggregation

Like neurons move together and form layers

Page 18: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

5. Synaptogenesis

Axons (with growth cones on end) form a synapse with other neurons or tissue (e.g. muscle)

Page 19: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

5. Synaptogenesis: Attraction to Target Cells

Target cells release a chemical that creates a gradient (dots) around them. Growth cones orient to and follow the gradient to the cells. The extensions visible in c are growing out of a sensory ganglion (left) toward their normal target tissue. The chemorepellent protein Slit (red) in an embryo of the fruit fly repels most axons.

Page 20: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

6. Neuron Death

•Between 40 and 75 percent of all neurons born in embryonic and fetal development do not survive.

•They fail to make optimal synapses.

Page 21: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

Neuron Death Leads to Synapse Rearrangement

Release and uptake of neurotrophic factors

Neurons receiving insufficient neurotropic factor die

Axonal processes complete for limited neurotrophic factor

Page 22: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

7. Synapse Rearrangement

•Active synapses likely take up neurotrophic factor that maintains the synapse

•Inactive synapses get too little trophic factor to remain stable

Page 23: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

7. Synapse Rearrangement

Time-lapse imaging of synapse elimination

Two neuromuscular junctions (NM1 and NMJ2) were viewed in vivo on postnatal days 7, 8, and 9.

Page 24: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

8. Myelination

Page 25: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

Myelination Lasts for up to 30 Years

Page 26: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

Brain Weight During Development and Aging

Page 27: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

Critical Periods

Page 28: Developmental Neuroscience Halo response of an embryonic chick ganglion after incubation with nerve growth factor. (Courtesy of Rita Levi- Montalcini)

Teratogens

Greek – “teratos” – wonder or monster

“genos” - birth

1. Physical agents (e.g., x-rays)

2. Chemicals (e.g., drugs)

3. Microorganisms (e.g., rubella)