Neurodevelopment (2) Flashcards

(22 cards)

1
Q

What happens after neurons migrate and form structures?

A

Axons and dendrites grow to connect with their targets. Growth cones at the tips guide them.

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2
Q

What are growth cones and filopodia?

A

Growth cones are the tips of growing axons/dendrites. Filopodia are fingerlike extensions that sense signals to guide growth.

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3
Q

What did Sperry discover with frog optic nerves?

A

Rotated frog eyes still sent axons back to the same target in the optic tectum, showing axons find precise targets.

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4
Q

What is the chemoaffinity hypothesis?

A

Each target releases a chemical label, and axons are attracted to their specific label to find the correct connection.

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5
Q

Why was the chemoaffinity hypothesis revised?

A

Axons follow specific routes guided by multiple signals along the way, not just a single chemical from the target.

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6
Q

What is fasciculation?

A

The tendency
of developing axons to grow along the paths established by
preceding axons is called fasciculation

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7
Q

What is topographic mapping?

A

Axons maintain spatial relationships from one neuron array to another (e.g., retina to optic tectum) even as structures grow.

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8
Q

What did studies on retinal-tectum regeneration show?

A

After optic nerve injury, axons grow to fill available space in an orderly way, not necessarily returning to their original points.

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9
Q

What is the topographic gradient hypothesis?

A

Axons grow from one topographic surface to another following intersecting signal gradients (e.g., anterior–posterior and medial–lateral) to maintain spatial maps.

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10
Q

What other mechanisms help axons map topography?

A

Spontaneous neural activity and neuron-astrocyte interactions also guide accurate connections.

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11
Q

What is synaptogenesis?

A

Formation of synapses between neurons after axons reach their targets.

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12
Q

How fast do synapses form during development?

A

About 700,000 synapses per second.

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13
Q

What is needed for synapse formation?

A

Coordinated activity between at least two neurons, chemical signals, spontaneous neurotransmitter release, and cell surface interactions.

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14
Q

How do glial cells influence synaptogenesis?

A

Astrocytes and microglia help form and maintain synapses, process information, and provide support (e.g., cholesterol for neuron growth).

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15
Q

What happens to synapses that don’t function properly?

A

They tend to be eliminated over time, ensuring only functional connections remain.

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16
Q

Why does neuron death occur during development?

A

More neurons are produced than needed; about 50% die in waves to refine neural circuits.

17
Q

What are the two types of cell death in neurons?

A

Necrosis: passive, messy cell death causing inflammation. Apoptosis: active, programmed cell suicide, safe and orderly.

18
Q

Why is apoptosis safer than necrosis?

A

Apoptotic cells are packaged in membranes that attract microglia to engulf them, avoiding harmful inflammation.

19
Q

What can happen if apoptosis is blocked or overactivated?

A

Blocked apoptosis → cancer; Overactivated apoptosis → neurodegenerative disease.

20
Q

What triggers apoptosis in developing neurons?

A
  1. Genetic programming for early death once neurons fulfill their function.
  2. Failure to obtain life-preserving chemicals (neurotrophins) from target cells.
21
Q

How do life-preserving chemicals from target cells influence neuron survival?

A

Extra target structures reduce neuron death; destruction of some neurons increases survival of remaining neurons.

22
Q

What are neurotrophins and their roles?

A

NGF (Nerve growth factor) and BDNF( brain-derived neurotrophic factor). They promote neuron growth, survival, axon guidance, and synapse formation.