Wiring the Visual System Flashcards

1
Q

what occurs at the optic chiasm

A

nasal hemiretina cross (contralateral hemisphere)
temporal RGC axons enter the ipsilateral hemisphere

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2
Q

midbrain projections

A

RGC - pretectum - pupillary reflex
RGC - superior colliculus - saccadic eye movements

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3
Q

central projections

A

LGN - primary visual cortex
(ipsilateral)

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4
Q

how are long range and short range cues sent

A

long range cues - secreted
short range cues - require physical contact

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5
Q

where is the retina made from

A

neural tissue (diencephalon)

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6
Q

retinal cell types

A

photoreceptors (1R 3C)
horizontal cells (inhibitory 2)
bipolar cells (around 11)
muller glial cells
amacrine cells
RGCs (>30)

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7
Q

layers of the retina

A

ONL
OPL
INL
IPL
GCL
optic nerve fibres

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8
Q

how is visual information processed

A

image
retina
visual input split into different information channels. Information channels defined by different circuits

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9
Q

what is the role of synaptic adhesion molecules

A

make connections

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10
Q

tenm3 MO

antinucci et al., 2013

A

cells don’t know where to interact

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11
Q

what are topographic maps

A

neuronal connections arranged such that neighbouring points in the origin are represented in adjacent locations in the CNS

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12
Q

regeneration experiment

Sperry 1963

A

remove dorsal retina = axons grow medially
remove ventral retina = axons grow laterally
remove anterior retina = axons grow posterior (bottom pair) tectum
remove posterior retina = axons grow to the anterior tectum

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13
Q

where does the retina project to the SC/tectum

A

nasal - posterior
temporal - anterior
dorsal - lateral
ventral - medial

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14
Q

frog with rotated eyes

A

temporal - anterior
nasal - posterior
dorsal - medial
ventral - lateral

if trying to catch fly, go up instead of down

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15
Q

what is the chemoaffinity hypothesis

A

specificity of wiring is based on chemical tags. Individual neurons express distinct molecular markers during development. Formation of appropriate synaptic connections depends on matching of complementary molecules on pre and post synaptic neurons.

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16
Q

3 principles of the chemoaffinity hypothesis

A
  1. neurons are instrincally different from eachother
  2. differences in position are biochemical
  3. differences are acquired early in development
17
Q

gradients in topographic maps

A

source gradient (confers identity)
target gradient (where)

18
Q

in vivo stripe assay

A

temporal retinal axons project to the anterior tectum (by attractive cues)
nasal retinal axons grow on both membranes

19
Q

ephrin A2/5 expression

A

temporal axons only avoid high ephrin A5
eph3 is the ephrina2 receptor

20
Q

removal of ephrinA

A

temporal: lots of receptors on the surface (high EphA conc), axons grow to posterior part
nasal: low EphA, not affected by EphrinA

21
Q

types of Eph receptors

A

tyrosine kinase family
A and B subtypes

22
Q

EphrinB1 expression in midbrain

Tectum

A

high medial
low lateral

23
Q

EphB2 expression in the midbrain

A

high ventral
low dorsal

24
Q

EphB-EphrinB mutant

A

ectopic termination zones found laterally

25
Q

repressive Wnt/Ryk gradient

A

retina: Ryk gradient high ventrally, low dorsally

tectum: Wnt gradient high medially, low laterally

26
Q

ryk mutant

A

no repulsion
100% medial growth

27
Q

stages of development of a retinotopographic map

A

PD0 - projections to back of brain
PD3 - refinement
PD8 - point to point connections, axons turn towards TZs

28
Q

formation of topographic map

A

axon extension and overshoot via EphA/EphrinA (repulsive)

topographic branching via EphA/EphrinA (repulsive)

branch guidance and aborisation via EphB/EphrinB/ryk/wnt (attractive and repulsive)

map refinement via ACh waves (dense TZ)