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Chapter 16 Continues

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Muscle membrane under the axon is the motor end plate and contains ... Plants do cyclosis stream around central vacuole circulate and mix cell contents ... – PowerPoint PPT presentation

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Title: Chapter 16 Continues


1
Chapter 16 Continues
2
Regulation by Ca2
  • Nerve has action potential that will elicit the
    muscle contraction
  • Nerve contacts at neuromuscular junction
  • Axon terminals contain acetylcholine
  • Muscle membrane under the axon is the motor end
    plate and contains acetylcholine receptors that
    are ligand gated channels
  • Message spreads by way of the transverse (T)
    tubule system that causes the SR to release Ca2
  • Muscle contraction

3
(No Transcript)
4
SR in Ca2 Release and Uptake
  • SR has 2 components medial element and terminal
    cisternae
  • Terminal cisternae releases Ca2 and also has
    high concentration of ATP-dependent Ca2 pumps
  • T tubule and terminal cisternae make up the triad
    connected by junctional complex
  • Ca2 released when action potential moves thru
    the T tubule system

5
Ca2 Release
6
Cardiac Muscle
  • Similar in structure to skeletal muscle
  • Difference 1 ATP energy comes from fatty acids
    rather than glucose, carried by serum albumin
  • Difference 2 not multinucleated, cells joined
    end to end by intercalated disc, electric impulse
    moves thru gap junctions to continue contraction

7
Smooth Muscle
  • Involuntary contraction
  • Slower than skeletal/cardiac contraction, lasts
    longer
  • Structure no striations, no Z-line, contains
    dense bodies

8
Smooth Muscle Contraction
  • Dense bodies are on the cell membrane and in the
    cytoplasm
  • Intermediate filaments and actin attach to the
    dense bodies and crisscross the length of the
    cell

9
Contraction
  • Increase in Ca2 leads to cascade of events
  • activates calmodulin and the Ca2-calmodulin
    complex activates myosin light chain kinase
    (MLCK)
  • MLCK phosphorylates myosin light chain
    (regulatory protein)
  • myosin makes filaments when phosphorylated
  • also activates myosin to interact with actin

10
MLCK Activation
11
MLCK Regulation
  • Autoinhibition
  • MLCK has a pseudo-substrate which prevents it
    from phosphorylating myosin light chain
  • Ca2-calmodulin complex prevents the
    pseudo-substrate from binding MLCK and therefore
    get phosphorylation of myosin light chain
  • Decreasing Ca2 levels activate myosin light
    chain phosphatase to remove the PO4 and again
    allowing the pseudo-substrate to bind

12
Actin-Based Motility in Non-Muscle Cells
  • Cell migration
  • Amoeboid motion
  • Ctyoplasmic streaming
  • Chemotaxis

13
Events of Cell Migration
  • Extension of protrusions on leading edge
  • 2 types
  • lamellapodia thin sheets of cytoplasm
  • filopodia thin pointed structures
  • Attach protrusions to substrate
  • Generation of tension to pull cell forward
  • Release attachment and retract tail

14
Migration
15
Lamellapodia Formation
  • Retrograde flow of F-actin bulk of movement of
    MFs is towards the rear of protrusion
  • 2 simultaneous processes
  • actin assembly towards protrusion
  • rearward translocation of actin to back of
    protrusion
  • Non-muscle myosin motor involved

16
Amoeboid Movement
  • Pseudopodia involved
  • Gelation and solation of actin cytoskeleton
  • 2 layers
  • outer gelatinous ectoplasm which is gel state
  • inner, more fluid endoplasm which is the sol
    state
  • Transition between gel or sol state

17
Cytoplasmic Streaming
  • Actomyosin-dependent movement
  • actin, also some specific myosins, ATP dependent
  • Happens in cells not doing amoeboid movement
  • Plants do cyclosis stream around central
    vacuole circulate and mix cell contents

18
Chemotaxis
  • Occurs usually on one side of the cell
  • Migrating cells move towards an increase or
    decrease in the concentration of diffusible
    substances
  • move to increase concentration is a
    chemoattractant move to high concentration
  • move to decrease concentration is a
    chemorepellant move away from high concentration
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