04 Wiring the Brain Flashcards

0
Q

Corticospinal and Corticobulbar tracts reside where in brain?

A

within Pyramidal tract.

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1
Q

What areas of the body have relatively greater representation in the cortex?

A

Areas for which there needs to be enhanced somatosensory sensitivity.

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2
Q

Describe how a phantom limb might be felt in another part of the body

A

if no sensation/information is being received by a part of the cortex (due to loss of limb), nerves from other parts of the cortex might grow into that place and infiltrate area of phantom.

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3
Q

One theory about the etiology of schizophrenia

A

disruption/improper migration of neurons. ALSO, deficits in signaling between neuregulin 1 and its receptor, ErbB4.

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4
Q

During cortical development, excitatory neurons derive from where? how do they migrate?

A

the pallium. Radial migration.

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5
Q

during cortical development, inhibitory neurons derive from where? how do they migrate?

A

derive from subpallium, migrate tangentially.

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6
Q

What are neuregulin 1 and ErbB4?

A

Neuregulin 1 is expressed in the pallium, guides inhibitory neurons which express ErbB4 receptors.

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7
Q

inhibitory neurons: what do they synthesize?

A

GABA. (neurotransmitter)

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8
Q

describe gamma oscillations. in what disease are they decreased?

A

gamma oscillations are an index of synchronized neural network activity. decreased in schizophrenia. impt for cognition, memory, learning.

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9
Q

what Calcium binding protein plays a big role in gamma oscillation frequency control?

A

parvalbumin. a set of fast-spiking GABAergic interneurons express parvalbumin.

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10
Q

parvalbumin interneurons rely on what for migration and differentiation?

A

rely on interneuron 1/ErbB4 signaling. Loss results in a decrease of power in gamma oscillatins that mimics the pattern seen in schizophrenia.

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11
Q

define the thalamocortical afferents (TCA). what guides them in their developmental path?

A

TCA: axon pathways between thalamus and cortex. corridor cells act as guideposts steering the growth cones of TCA cells as they traverse the developing brain.

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12
Q

describe the path of corridor neurons.

A

derive from the LGE (lateral ganglionic eminence) but migrate into MGE. Form a permissive zone between MGH and primordial globus pallidus (which would normally repel TCAs). Corridor cells express neuregulin1, and TCAs growth cones express ErbB4.

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13
Q

describe guidepost cells. how do they guide pioneer neurons?

A

guidepost cells act as kiosks for pioneer neurons that grow from the periphery to the CNS. Growth cones of pioneer neurons are guided by guidepost cells

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14
Q

name 3 types of guidepost cells in vertebrates

A
corridor neurons (thalamocortex)
Cajal-Retzius cells (hippocampus)
subplate neurons (cortex)
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15
Q

what are the main excitatory cells called?

A

principal cells.

16
Q

name 2 features of growth cones.

A

lamellipodia (sheet like structures)
filopodia (finger like projections)
highly specialized structures that direct the movement of the growth cone.

17
Q

general qualities of axon guidance molecules that are SECRETED?

A

tend to be long-range signals, expressed as gradients in target tissue.

18
Q

general qualities of axon guidance molecules that are TETHERED?

A

tend to be short-range signals, local acting.

19
Q

Feature of pioneer neurons?

A

have many active filopodia. some of pioneer neurons are transitory, and will be primary sensory cells until other cells follow and replace them.

20
Q

Trophic molecules vs tropic molecules?

A

Trophic: support growth and survival
Tropic: guide
some molecules function as both

21
Q

Describe ECM molecules. examples?

A

ECM = extracellular matrix. proteinaceous molecles, interact with receptors (integrins) in the axons to regulate the extent of adhesion of the growth cones.
Examples: laminin, fibronectin.

22
Q

how do axons change their sensitivity to ECM proteins?

A

alter expression of integrins. (receptors that interact with ECM molecules).

23
Q

what are CAMs?

A

Cell Adhesion Molecules. bind to promote adherence amongst axon processes. expressed by both pioneer and follower axons.

24
Q

Netrin: receptor is what?

A

DCC

25
Q

Slit: receptor is what?

A

Robo

26
Q

Semaphorins: receptor is what?

A

Various neuropilins and plexins

27
Q

Ephrins: receptor is what?

A

Eph

28
Q

Netrins are impt for what? Receptors expressed where? Netrins expressed by what cells/where?

A

Netrins are multifunctional, can either repel or attract depending on circumstance. Receptors are DCCs. Receptors expressed in retinal ganglion cell axons. Netrins expressed by midline floorplate neurons at optic chiasm.

29
Q

Netrin turning response is dependent on what?

A

Dependent on cAMP concentration in growth cone.
If HIGH, attraction
if LOW, repulsion.

30
Q

Slit is expressed where, by what cells? Receptor is what? Role is what?

A

Expressed by midline floorplate neurons at optic chiasm. Can be multifunctional. Receptor is Robo. Slit plays role in preventing ipsilateral axons from crossing at optic chiasm, and preventing REcrossing from crossed axons.

31
Q

Semaphorins are expressed where? Can cause what? Receptors are what? Receptors expressed where?

A

Semaphorins expressed on cell surfaces or ECM (can be either secreted or membrane bound). Can cause immediate growth cone collapse. Receptors are various neuropilins and plexins, some expressed on growth cones.

32
Q

Ephrins do what?

A

Regulate formation of topographical maps in retina and tectum.

33
Q

Which ephrins regulate Anterior-Posterior topography?

A

Ephrin A and EphA receptors. Cells with lowest Ephrin A map to axons with highest EphA receptors.

34
Q

Which ephrins regulate Dorsal-Ventral topography?

A

Ephrin B and EphB in retina and tectum. Signals are purely attractive.

35
Q

Ephrins exist where in the brain? their receptors exist where?

A

Ephrins exist on tectum (colliculi).

Eph receptors exist on retinal ganglion cell axons.

36
Q

At choice points, what happens morphologically to filopodia?

A

The whole axon growth cone slows when it senses a choice point, and filopodia extend outwards.