3. Neuronal cell biology Flashcards

1
Q

What are the 4 points of the neuronal doctrine?

A
  1. The neuron is the structural and functional unit of the nervous system
  2. Neurons are individual cells not continuous to other neurons
  3. The neuronal has 3 parts; dendrites, soma and axon
  4. Conduction is from dendrites to some to end of axon
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2
Q

Function of dendrites

A

Increase SA and receive outputs

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3
Q

Function of axon

A

Carry information over long distances

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4
Q

Function of hillock

A

Action potential origin

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5
Q

Function of myelin

A

Coats axons, improves conductance

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6
Q

Node of Ranvier function

A

Break in myelin sheath

Allows saltatory conduction

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7
Q

Terminals function

A

output region
transmitter release
synapse with other neurones

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8
Q

In which direction is retrograde transport?

A

Terminals to axon to soma

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9
Q

In which direction is anterograde transport?

A

soma down axon to terminals

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10
Q

Speed of retrograde transport

A

5 mm per day

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11
Q

Speed of anterograde transport

A

rapid 300-400 mm per day

slow 5-10 mm per day

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12
Q

Oligodendrocyte function

A

form myelin sheath

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13
Q

Microglial cell function

A

scavengers

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14
Q

Astrocyte function

A

mop up neurotransmitters

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15
Q

What neurotransmitters can glia release?

A

ATP, glutamate

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16
Q

Which NS are oligodendrocytes responsible for myelin?

A

CNS - wrap over parts of 50 neurons

17
Q

What causes myelin in the PNS?

A

Schwann cells wrap part of a single neuron

18
Q

Major proteins in CNS myelin

A

PLP

19
Q

Major proteins in PNS myelin

A

P0 and PMP22

20
Q

What do mutations in PLP cause in mice, rats and humans

A

mice - jimpy, shaking pup, rump shaker
rats - md
humans - Pelizaeus-Merzbacher Disease

21
Q

What do Th cells do in EAE?

A

Cause demyelination, chronic relapsing paralysis.

22
Q

Why does EAE result?

A

Mutation in T cell receptor gene V beta 8.2

23
Q

What can demyelination cause?

A

MS
CMT
Adrenoleukodystrophy

24
Q

What does a defect in P0 and PMP22 cause?

A

CMT

25
Q

How do the long chain fatty acids build up in ALD?

A

A deficiency in the peroxisomal enzyme catalyzing formation of lignoceroyl-CoA ligase
Defect in a peroxisomal membrane protein needed to import the ligase into the peroxisome