Muscle Tissue (Histology) Oct30 M3 Flashcards

1
Q

shape of the SR in striated muscle

A

regular. has tubules (segments of SR) and cisternae (lateral sacs of SR)

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2
Q

T-tubule def

A

invagination of the plasmalema that goes very deep in cell

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3
Q

SR cisternae name near T-tubule

A

terminal cisternae

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4
Q

Triad def.

A

cisterna-T tubule-cisterna combination

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5
Q

what is found between adjacent cisternae (SR component)

A

connecting tubules of SR

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6
Q

location of triad in SKM

A

at junction of A and I band.

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7
Q

location of triad in cardiac muscle

A

near Z line

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8
Q

what is found at the terminal cisternae + function

A

Calcium ATPase (Ca pump) pumps Ca in the SR

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9
Q

What makes the Ca release from the SR

A

depolarization of the membrane due to membrane potential coming from outside, via the T tubule

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10
Q

perimysium appearance on cross section

A

appears enlarged (histology artefact) bc tissue was put on hot plate for it to spread

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11
Q

On EM, what we see between adjacent myofibrils within the cytoplasm

A

mitochondria and glycogen molecules that appear as dark dots

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12
Q

T-F: axon myelinated in SKM NMJ + explan.

A

True. Myelinated by Schwann cells that form myelin sheaths

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13
Q

appearance of postsynaptic membrane (sarcolema) in NMJ

A

is folded.

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14
Q

space name between pre and post synaptic membrane at NMJ

A

synaptic cleft

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15
Q

other name for NMJ

A

terminal button

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16
Q

NMJ neurotransmitter

A

ACh

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17
Q

cardiac muscle NMJ neurotransmitter

A

Ach if PSS

NE if SS

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18
Q

SKM NMJ postsyn. receptor nd function

A

AchR, binds Ach. Makes Na+ flow in and K+ flow out

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19
Q

AchR type of receptor and conformation

A

ligand-gated. 5 subunits: two alpha, 1 gama, 1 beta, 1 delta encoded by diff genes

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20
Q

Why do we say that the AchR at the NMJ is immunologically protected

A

No Abs normally produced against it

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21
Q

Myastenia gravis cause (autoimmune disease)

A

Ab produce against AchR at NMJ

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22
Q

AChE function at the synaptic cleft

A

splits ACh into acetate and choline, both recycled by presynaptic neuron

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23
Q

location of BM at NMJ

A

BM of striated muscle is continuous with BM of Schwann cells (which wraps around axon) and doesn’t enter T tubules. Also no BM between Schwann and axon

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24
Q

heart layers from outside to inside (not only heart wall)

A

fibrous pericardium, serous pericardium (parietal lamina and visceral lamina or epicardium), myocardium, endocardium

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25
three layers forming the wall of the heart
epicardium (visceral lamina of serous pericardium), myocardium, endocardium
26
fibrous pericardium charact.
CT around the heart (external capsule)
27
epicardium charact.
covers the heart and part of the blood vessels
28
myocardium charact.
thickest part of heart wall. made of cardiac muscle fibers (cells)
29
endocardium charact.
thin membrane of endothelium, CT and SM tissue
30
percardial cavity separates what layers
parietal lamina of serous peric. and visceral lamina (epicardium) of serous peric.
31
what muscle type has cells that sometimes branch
cardiac
32
what muscle type has highest density of capillaries
cardiac muscle
33
what is the BM at intercalated disks
is in fact two BMs that attach
34
two portions of intercalated disks
north south portion and east west (or west east) portion
35
3 junction zones at ICs and which part of IC they're in
Zonula adherens and macula adherens (desmosome) in north south Gap junction in east west portion
36
Zonula adherens charact
''Z line like'': alpha actinin at the plasmalema anchors F-actin
37
Desmosome (macula adherens) charact
plaque with proteins called plaquoglobins and intermediate filaments anchoring there
38
Gap junction charact.
The 2 BMs become very close. Interaction between them bc have pores there
39
Gap junction pores names and components
connexons. each has 6 connexin molecules
40
heart: type of connexin molecule and consequence of mutation
connexin 48. mutation is lethal.
41
gap junction function
allow passage of ions of calcium
42
why gap junctions necessary in cardiac muscle
Ca flows between the cells so available everywhere. as in Ca available to all the troponin in SKM
43
cardiac muscle: why SR is complex
- sometimes have terminal cisternae, sometines not | - sometimes have triad at level of Z line, sometimes not
44
cardiac muscle SR similarities with SKM SR
T tubules, calcium pump
45
why difficult to see myofibrils in SM
mainly actin there and not much myosin. + not organized in sarcomeres
46
something special happening in SM at contraction
shape of nucleus changes
47
special structure at sarcolema of SM
vesicles that don't detach called caveoles (that could do function of T tubules?)
48
what do we see outside SM cells near them (equivalent to endomysium)
reticular fibers
49
Dense bodies on SM cells plasma membrane: what they are
contain alpha actinin like proteins achoring the actin filaments (are rich in alpha actinin) (Z line like)
50
SM mechanism of contraction: what Ca does
binds myosin light chain kinase (MLCK)
51
SM mechanism of contraction: what MLCK does
phosphorylates the light chains of the myosin to displace the head previously attached to the tail. Head can bind acin
52
SM mechanism of contraction: how close myosin is to actin and how myosin is organized in SM cell
myosin close to actin b4 contraction but doesn't bind. Myosin is as individual molecules
53
SM speed of contraction and what this makes it good for
slow. makes it good for peristaltic movement, lumen contraction of blood vessels.
54
how SM shape changes from before to after contraction
more elongated to more round and less elongated
55
SM relaxation: how
Ca levels decreased, inactivation of MLCK.
56
Ehlers-Danlos syndrome affects what + consequence
affects CT, joints and vessel walls. Severe form called vascular Ehlers-Danlos causes walls of blood vessels, intestines or uterus to rupture
57
Ehlers-Danlos syndrome cause
mutation of reticular fibers. causes wall ruptures (in aorta, digestive system, etc.)
58
Myasthenia gravis: symptoms and explanation
fluctuating muscle weakness and fatigue. The Ab binding to AchR inhibits the excitatory effect of Ach on AchR at the NMJ
59
Muscular dystrophy: give two types
Duschenne and Becker
60
Muscular dystrophy: two mutations that can give that
mutation in laminin or dystrophin
61
what dystrophin does + associated diseases
DMD. BMD. is at muscle fiber membrane. links actin to dystroglycans in sarcolemma which are linked to laminin.
62
what laminin does
Are part of the basement membrane. interacts with dystroglycans at the sarcolemma