Axonal Growth Lec03 Flashcards

(79 cards)

1
Q

____ changes shape at decision points

A

growth cone

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2
Q

how do neurons start (before polarization)?

A

round, with no obvious processes

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3
Q

___ defines the polarity of the neuron

A

the axon

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4
Q

where are growth cones located?

A

the tip of the axon

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5
Q

what are lamellapodium?

what do they contain?

A

fan shaped sheet at the tip of the axon

contain actin filaments and microtubles

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6
Q

what are filopodia? what do they contain?

A

fine processes extending out from lamellapodium

have actin filaments

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7
Q

___ growth cone form and disappear rapidly

A

filopodia

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8
Q

___ dictates direction of growth - in lamellipodia / filopodia

A

Filamentous actin (F-actin)

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9
Q

____ gets incorporated into F-actin at leading edge

A

Gobular actin (G-actin)

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10
Q

F-actin Binding Proteins cause ___ and ___

A

retrograde flow & growth cone turning (by causing depolymerixation)

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11
Q

attractive cue increases ___ and decreases ___

A

↑ polymerization/assembly, ↓ retrograde flow (goes toward the attractive cue)

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12
Q

functional difference ebtween MT and F-actin

A

MT are responsible mostly for axon elongation

f-actin dictates direction

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13
Q

___ make the cytoskeleton core

A

Microtubules (they are strong and stable)

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14
Q

Acetylated microtubles only in ____

A

axons

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15
Q

Tyrosinated microtubules ↑ in ____

A

lamellipodia

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16
Q

where is f actin found?

A

in lamellipodium and filpodia

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17
Q

Contact repellants include

A

Semaphorins and Ephrins

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18
Q

Contact attractants include

A
  1. peipheral ECM
  2. CAM
  3. Cadherins
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19
Q

___ are attractants inthe periphery, but are not well understood in the CNS?

what are examples of each?

A

ECM molecules

attractants - laminins, collagens, fibronectin

not well understood? repellants? – proteolgycens, glycoproteins, hyaloruonan

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20
Q

homolphilic binding of Cam

A

triggers cytoplasmic kinases of growth cone

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21
Q

what is Ca independent signaling? dependent

A

indepdent - CAM

Depdendent - caDherins

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22
Q

homophilic binding of cadherins triggers

A

intracellular signals –> actin binding &
organization

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23
Q

axon guidance signsla re either ___ or ___

A
  1. nondiffusable and short range
  2. or diffusable and long range
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24
Q

the contact attraction and repulsion signals are ___

A

nondiffusable and short range

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25
the chemoattractants and chemorepulsive signals are
diffusable and long range
26
what does the binding of axon guidanc emolecules to receptors on growth cones activate?
signaling cascades that result in the reognization of growth cone cytoskeletons --\> controlling **_the direction and rate at which the growth cone moves_**
27
attractive interactions (contact attractants and chemoattractants) promote \_\_\_\_
actin polymerization
28
repellant interactions promote \_\_\_\_
actin depolymerization and growth cone collapse
29
lamins, collagens, and fibronectins bind to \_\_\_
integrin receptors
30
\_\_\_ has been associated with bundling (fasiculation) of groups of axons as they grow
L1 CAM
31
where can cadherins be found
on the suface of growth cones, growing axons, surrounding cells or targets
32
where are semapghorins found?
can be secreted or anchored to the cell surface (secreted are probably attached to the cell surface or the ECM --\> not really diffusable)
33
where do sempahorins bind to?
cell surface --\> plexin family receptors secreted --\> bind neurophilins
34
what is the difference between the two classes of ephrins?
ephrin A has gpi linked ot surface ephrin b is a single pass transmembrane protein each has its own receptors on growth cone
35
why do temporal retina axons go to the anterior tectum?
ephrins A2 and A5 are lower in anterior -\> posterior A2 and A5 repulses the temporal axons since they have high A3
36
nasal retina go to the posterior tectum because
axons from the nasal retina are blind to ephrin and lack the eph receptor so they don't be repulsed by ephrins A2 and A5 found highly in the posterior tectum
37
chemorepulsion molecules include
slits netrins if they have UNC 5 receptors
38
chemoattractant molecules include
netrin if they have DCC receptors
39
what is secreted at the embyro midline
chemorepulsants, so netrins and slits
40
what are slits receptors
robo
41
what receptors make netrin attractants
DCC
42
what receptors make netrin repiulsants
UNC 5
43
before crossing the midline ___ attracted to netrin at midline
DCC
44
after crossing the midline --\>
cell upregualtes robo receptors, repulsion from the midline
45
what silences DCC signaling?
the robo that is upregulated after crossing
46
what does KO of netrin eliminate?
the crossing of commisural axons
47
why do netrin and silts have to work together?
because the cells have to cross at a very specific site in the spinal cord also cant recross
48
synaptogensis in CNS Presynaptic process (from growth cone) recognizes target cell via \_\_\_\_
cadherin
49
start of synaptgensis at the NMJ?
**1. mtoor axon approaches and amkes contact with a myotube**
50
in synaptogensis at NMJ after mtoor axons approaches the myotube.... what happens?
nerve terminal and mytotubual diffeerentiate nerve terminal becomes motor terminal muscle forms post synpatic apparatus
51
what is the differenation of muscle induced by?
agrin --\> activating MuSK --\> causing clustering and increased expression of acetylcholine receptors
52
what does MuSK do?
causes clustering and increased expression of acetylcholine receptors
53
in NMJ synaptogensis, both the motor nerve and muscle make
ecm components to form a basa lamina (to stabilize the synaptic structure)
54
axons arising from **_t1_** in the superior cervical ganglia form synapses on cellbodies of neurons that
project to targets in the eye
55
axons arising from **_t4_** in the superior cervical ganglia form synapses on cellbodies of neurons that
project to targets in the ear
56
how do the correct pre and post synaptic neurons in superior cervical ganglion find eachother
they have a higher affinity than the wrong combinations
57
CNS synaptogensis what recognizes the appropriate site on target cell
nascent presynaptic process via cadherin/protocadherin family
58
CNS synaptogensis ## Footnote immediately after nascent process recognizes the target cell --\>
synaptic vesicles and active zone components accumulate
59
CNS synaptogensis ## Footnote what is recruited in the developing synapse tob ring in moilecules?
neurexin and neuroglin
60
where is neurorxin found? what is its function
presynatpic function -- localizes cytoskeltal elements, vesciles, active zone proteins, and Ca channels TO PRESYNAPTIC MEMBRANE
61
where is neuroglin found? what is its function?
postsynp. membrane function -- recruits NT receptors and other postsynatpic proteins
62
After synaptogenesis, target cells secrete
limited amounts of neurotrophic factors.
63
which neurons survive after synaptogensis?
those that receive enough trophic factors
64
Neurotrophins control the
of target cells contacted and # of synapses formed
65
what happens if there is NGF in check sensory ganglion? if there is none?
yes NGF -- explosion of axon extensions no NGF -- neuron death
66
\_\_\_ respond to all growth factors
dorsal root ganglion
67
nodose ganglia respond best to
NT3
68
Sympathetic ganglia respond best to \_\_\_? and not at all to \_\_\_?
best to -- NGF not at all to BDNF
69
neutrophin receptors include --
Trk and p75 receptors
70
Trk receptors ahve a high affinity for
processed/cleaved neutrphins
71
p75 have a high affinity for
unprocessed enutrophin
72
intially, skeletal muscle and some aprsymp neurons are innveratvated by
multiple neurons | (this is eventually pruned)
73
with synapse elimation at the nmj, comeptition is dependent on
electricial activity in both pre and post synaptic cells
74
blocking electrical acitivity in either pre or post synaptic cells results in
persistence of polyneuronal innervation
75
axonal branching patterns are refined via
competition and synapse elimination
76
BDNF, NT3, NT 4/5 are all
growth factors
77
what is evidence for the trophic function of NGF?
no NGF --\> neuronal death excessive NGF --\> survival of excess neurons NGF are present (and produced) in target cells) NGF
78
neutrophic interactions depend on
neurotrophins secreted by target cells the neurorophin receptors present intracellualr signaling cascade present
79
neutrophic interactions determine--
number of neurons, shape of neurons, patterns of neuronal connections