Muscle Flashcards

1
Q

Muscle Types

A
• SKELETAL MUSCLE
     o Striated muscle
     o Nuclei peripherally located
     o Large cells, multinucleated
    o Strong, quick discontinuous voluntary contraction
• CARDIAC MUSCLE
     o Striated muscle
     o Shorter/stubbier 
    cells than skeletal 
    muscle
    o About twice as long 
       as they are wide
    o Centrally located 
       nucleus (usually 
      single nucleus, 
      sometimes 2)
    o Strong, continuous involuntary contraction
• SMOOTH MUSCLE
    o Tapered, overlapping, non-striated
   o Centrally located nucleus
  o Weak, slow involuntary contraction
  o Either continuous or discontinuous depending on the organ
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2
Q

Skeletal Muscle Packaging

A

• Skeletal muscle has to have packaging from outside to inside

• Bundles of MYOFIBRILS make up A MUSCLE FIBER, and bundles of muscle
fibers make up a MUSCLE

  • Myofibrils are made up of organized filaments
  • In muscle, the term FIBER is a CELL
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3
Q

Skeletal muscle connective tissue covering

A
  • EPIMYSIUM: dense CT around muscle
  • PERIMYSIUM: dense CT around fascicle

• ENDOMYSIUM: delicate CT around fiber
o Comes together at the ends of muscle cells and whole muscles to give rise to tendons

• There are blood vessels in the connective tissue – can see capillaries in
cross section located in the endomysium

• There are SATELLITE CELLS in the basement membrane (marked with Pax7)
o The younger you are, the more satellite cells
o Satellite cells play an important role in healing

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4
Q

Development of skeletal

muscle

A
  • Myoblasts
  • Satellite cells: source of stem cells in adult muscle that can repair damage
  • Skeletal muscle cells grow by hypertrophy (cells get bigger) – not by hyperplasia (making more cells)
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5
Q

Molecular events
regulating muscle satellite cell activation during skeletal muscle
regeneration

A

• Quiescent satellite cells are seen in a resting myofiber (expressing Pax7, a
well-known MRF transcription factor expressed in quiescent satellite cells)

• Following damage, the myofiber, satellite cells are activated to enter the cell cycle and proliferate allowing for expansion of the myogenic cell
population

• These activated satellite cells are characterized by high expression of
MRFs, MyoD and Myf5

• The proliferative phase is followed by Myoblast terminal differentiation
and characterized by the upregulation of the MRF’s, Myogenin and Mrf4

• New myofiber formation (upon innervation)

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6
Q

Skeletal muscle

organization

A

• SARCOMERES: repeating
contractile units

  • A band: anisotropic, dark band, composed of thick filaments, myosin
  • I band: isotropic, light band, thin filaments, actin
  • Z line: in the center of the I band, sarcomere is from Z line to Z line
  • H zone: in the center of the A band
  • M line: in the center of the H zone
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7
Q

THIN FILAMENTS of

Skeletal Muscle

A
  • F-Actin: filaments of actin embedded in the Z line
  • Tropomyosin: filamentous protein that fills the groove in F-actin and binds troponin

• Troponin:
o TnT: troponin subunit that binds tropomyosin
o TnC: troponin subunit that binds calcium
o TnI: troponin subunit that inhibits actin-myosin interaction

  • Alpha-actinin: actin linking protein located at the Z line
  • Desmin: intermediate filament located in muscle
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8
Q

TITIN

A
  • Very large molecule that runs along myosin and binds to itself on the M line
  • Gives some stress tolerance and stability
  • Affects the overall flexibility of the muscle cell
  • Keeps cells from being overstretched
  • Has some recoil activity to set the structure of the cell
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9
Q

Sacroplasmic Reticulum

A

• Sarcoplasmic reticulum: special SER in muscle that sequesters and releases calcium

• Components:
o Terminal Cisternae: I band, calciquestrin
o Tubular Channels: A band
o H Sacs: H zone
o T-Tubules: penetrations of the cell membrane deep into the muscle cell cytoplasm

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10
Q

Myasthenia Gravis Clinical

Manifestations

A
  • Inability to focus the eyes (extraocular muscular paresis)
  • Drooping eyelids (ptosis) à levator palpebrae superioris; CN III
  • Double vision (diplopia) à extraocular muslces; CN III, IV, VI
  • Difficulty in chewing&raquo_space; CN V
  • Difficulty in swallowing (dysphagia)
  • Slurring of words (dysarthria)
  • Limb weakness (10%)
  • Progressively worsens throughout the day

• Treatments:
o Cholinesterase Inhibitors
o Corticosteroids
o Immunosupressants

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11
Q

Muscular Dystrophy

A

• Predominantly affects young males

• Dystrophin gene is defective
o Large complex, located underneath cell membrane in skeletal
muscle
o ECM components = type IV collagen/laminin bind to series of
glycan molecules > bind to the sarcoglycan complex > bind to
dystrophin and host of internal molecules reinforce
cytoskeleton
o Function: reinforce muscle
membrane because skeletal muscle is under a lot of mechanical force

• Without dystrophin, mechanical
forces manipulate the
transmembrane binding molecules > rips a hole in the membrane >
hypercontraction of the muscle > cell death

• Muscle heals via satellite cells but
over time, you have fewer satellite
cells until they eventually deplete and most of your muscle cells get replaced by fat

  • Few remaining muscle cells are huge in diameter compared to normal because they’re hypertrophying to compensate for lack of satellite cells
  • Eventually can no longer replace muscles in the diaphragm so they can’t breathe anymore – patients usually die young
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12
Q

Cardiac Muscle

A
  • MYOCYTES: muscle cells
  • CYTOPLASM: full of organelles, myofibrils
  • STRIATIONS: not as distinct as in skeletal muscle
  • NUCLEI: centrally located
  • MYOFIBRILS: not as uniformly distributed as skeletal muscle
  • MITOCHONDRIA: abundant and interspersed in cytoplasm
  • BRANCHING and ANASTOMOSING fibers
  • SARCOPLASMIC RETICULUM: less defined than in skeletal muscle
  • INTERCALATED DISCS: at sarcomere ends, connect myocytes
  • PURKINJE FIBERS: close to endocardium, specialized cardiac muscle cells
  • Heart Impulse Conduction System

• MYOENDOCRINE CELLS: cardiodilatins (CDD) or atrial natriutetic
polypeptides
- vasodilation

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13
Q

Integrin

A
  • Col I and II binds near the Z line to individual muscle cells
  • Integrins bind the collagen

• Beta chains that pass through the cell
membrane and bind to the small cytoplasmic domain

• Bind to a host of molecules underneath
the cell membrane

• Dystrophin doesn’t exist in the heart, instead it has integrin + vinculin complex which has a similar adhesion function

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14
Q

Intercalated Disc

A

• On the vertical portions: has FACIAE ADHERENS – similar to zonula adherens found in cell junctions

• The whole end of the cell where the sarcomere is binds through the faciae
adherens to the end of the next cell

• On the horizontal portions, there are gap junctions

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15
Q

Conduction system

A
  • AV bundle of His penetrates cardiac skeleton

* Purkinje fibers – bigger muscle cells that spread excitations quickly

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16
Q

Smooth Muscle

A
  • LOCATION: tubular organs
  • FORM: spindle shaped
  • SIMILAR CELLS: myoepithelial cells, pericytes
  • LIGHT microscope structure: elongated, nonstriated, overlapping
  • THIN FILAMENTS: 30-80 A, composed of actin

• DARK PATCHES: cytoplasmic dense bodies,
sub plasmalemma dense
plaques

• ANCHORING FILAMENTS: 100A, desmin intermediate filaments, links
together bodies and plaques

  • THICK FILAMENTS: 120-160 A, composed of myosin
  • SLIDING filament mechanism: calmodulin dependent