Growth Cone Flashcards

1
Q

What did Ramon y Cajal do?

A

He studied the growth cone and described it as protoplasm of conical form that is soft and flexible, but contains motility where it pushes aside obstacles until reaches the region of its peripheral temrination

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2
Q

What did Harrison do?

A

In 1907, Harrison showed in tissue culture experiments that growth cone is indeed motile

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3
Q

What did Speidel do?

A

In 1933, Speidel also confirmed motility by in vivo live observation of growth cones in tadpole tails.

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4
Q

What did Yamada do?

A

In 1970, Yamada revealed the cytoskeletal structures and their importance by EM studies.

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5
Q

What is the definition of the neuronal growth cone?

A

It is a highly motile structure at the tip of growing axons and dendrites. It recognizes guidance information/cues in the embryonic environment and transduces it into directed movement towards the target cell.

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6
Q

What are growth cone functions?

A
  1. Sensing
  2. Signaling
  3. Be motile and do directional movement
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7
Q

What are molecular components of sensing?

A

receptors for cues

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8
Q

What are molecular components of signaling

A

signaling enzymes (kinases and RHO GTPases)

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9
Q

What are molecular components of motility?

A

cytoskeletal and associated proteins

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10
Q

What is filopodium?

A

spiky parts of growth cone where F-actin sticks out

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11
Q

What is lamellipodium?

A

flat f-actin meshwork of growth cone

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12
Q

What are the three major regions of growth cone?

A

A) Peripheral Domain (F-actin rich)
B) Transition zone
C) Central Domain (microtubule rich)

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13
Q

Size and morphology depend on a number of factors, such as:

A
  1. neuronal cell type
  2. species
  3. substrate and cell culture conditions
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14
Q

How do filopodia and lamellipodia explore their space?

A

extension and retraction

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15
Q

What do retinal ganglion cells cross to go into the brain

A

Optic Tectum

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16
Q

What are the different F-actin structures?

A
  1. filopodial actin bundles
  2. lamellipodial networks
  3. transverse actin arcs in transition zone (keep microtubules in central domain)
  4. ruffles (intrapodia) in transition zone
17
Q

Where do you find microtubules

A

Mainly in the C domain, although dynamic MTs in P domain

18
Q

Where do you find F-actin?

A

mainly in the P domain

19
Q

What do they use to quantify cytoskeletal dynamics?

A

(FSM) - Fluorescent Speckle Microscopy

20
Q

What allows motility?

A

Actin filaments attach to substrate. Myosin which attached to microtubule attempts to pull f-actin back but instead pulls microtubule forward

21
Q

What drug blocks actin assembly

A

Cytochalasin B, it slows down growth

22
Q

What is the role of F-actin vs microtubules?

A

They are both important for growth cone guidance. F actin is more for motility. While microtubules for axonal outgrowth.