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140 Cards in this Set

  • Front
  • Back
epimysium
the connective tissue covering the whole muscle
perimysium
the connective tissue covering of the muscle bundle/fascicle
endomysium
the connective tissue covering of the muscle fiber
actin
this protein is located in the thin filament; binds to myosin to produce a cross bridge
alpha-actinin
this protein anchors actin to the Z disc in the sarcomere
Laminin
this protein is located in the lamina lucida layer of the basal lamina; it contributes to cell attachment (exists with the costamere)
myosin
protein located in the center of the sarcomere, and is the major component of the thick filament; it binds to actin to produce a cross bridge
tropomyosin
protein located in a groove along the length of the actin filament; it covers the myosin binding sites on actin to prevent cross bridges from being formed
troponin
protein that is bound to both actin and tropomyosin; when calcium binds to it, tropomyosin changes and the actin binding sites are exposed so cross bridges can be formed
nebulin
protein that is connected to actin; appears to contribute to assembly and regulation of thin filament length
titin
this protein connects myosin filaments from the M line to the nearest Z disc; it maintains myofibrillar lattice structure and contributes to the passive tension of the muscle
Z discs
these are the dark lines that bisect the I bands of thin filament; demarcate the sarcomere
M line
the dense zone in the center of the A band of thick filaments
myosin binding proteins
proteins that provide a framework/scaffold to stabilize thick filament and guide the filament development during myogenesis
desmin
this is a protein that is the major part of intermediate filament system; it connects the outer Z disc to the sarcolemma and also tethers the Z disc to the mitochondria and myonuclei; it plays a critical role in maintaining registry between adjacent Z discs
dystrophin
protein located in the subsarcolemmal region; it stabilizes the membrane ion channels during contraction and relaxation; it links the dystrophin associated proteins to actin
dystrophin associated proteins
this protein complex spans the sarcolemma and is thought to play a critical role in linking the actin cytoskeleton to the extracellular matrix
costamere
these structures are located below the sarcolemma; they couple force-generating sarcomeres with the sarcolemma and anchor the sarcolemma with the Z discs, M lines, and at the musculoskeletal junction
creatine kinase
this is an enzyme located within the thick filament that helps to regulate ATP levels in the muscle cell
basal lamina
this membrane forms a network that links skeletal muscle proteins to the sarcolemma, providing lateral transmission of force; it maintains muscle integrity as well. It is required for muscle repair and is a selective permeability layer
DHP receptors
these receptors are located in the T tubule; they sense the change in voltage during an action potential
RyR
these receptors are located on the sarcoplasmic reticulum and are a calcium release channel
calsequestrin
this protein is located in the sarcoplasmic reticulum; it binds and stores calcium
SERCA
this is a calcium ATPase transporter that pumps calcium back into the SR
phospholamban
this is a protein that regulates the activity of SERCA (when phosphorylated, increases SERCA activity)
myoD myfd5
these myogenic regulatory factors are involved in determination (create myoblasts)
mrf4 and myogenin
these myogenic regulatory factors are expressed later and are involved in differentiation (cause myoblasts to proliferate and fuse into myotubes for muscle development to proceed)
plasma membrane
this cell organelle separates the interior of the cell from the outside; it is an attachment point for the intracellular cytoskeleton; it attaches the ECM to other cells to help group the cells together to form tissues
mitochondria
this cell organelle generates most of the ATP used to supply the cell; it regulates cell metabolism and can regulate homeostasis of calcium and membrane potential
myonuclei
these organelles are responsible for a "domain"; they secrete different growth factors that support growth and repair of the cell
sarcoplasmic reticulum
this organelle is directly involved in the storage of calcium and the removal of calcium from myofilaments to relax muscle; it is the middleman between skeletal muscle activation and relaxation
twitch
the response of one single muscle fiber to a single action potential
unfused tetany
when a set of repeating action potentials activates the muscle fiber before the relaxation of the previous twitch; can still distinguish between contractile events
fused tetay
the time interval between activation of successive twitches has shortened and the twitches fuse into a single, stable level of muscle
motor unit
the alpha motor neuron and all the fibers it innervates
calcineurin/NFAT
the main pathway for myofiber transition
Akt, mTOR
the main pathways for muscle hypertrophy
myostatin, FOXO, urfs, atrogin, ubiquitin ligase
the main pathways for muscle atrophy
Akt
these proteins inhibit cell apoptosis and can also induce protein synthesis pathways, so it is therefore a key signaling protein in the cellular pathways that lead to skeletal muscle hypertrophy
atrogin
this protein mediates proteolysis events that occur during muscle atrophy; it is thought to recognize and bind to some proteins to promote their degradation during atrophy
mTOR
this protein integrates the input from pathways, senses cellular nutrient and energy levels and determines if there is enough to cause hypertrophy
myopathy
a muscular disease in which the muscle fibers do not function for reasons, resulting in muscular weakness
sarcopenia
the degenerative loss of skeletal muscle mass and strength that is associated with aging
NCAM
this molecule is expressed on the primitive myotubes following denervation to perhaps "guide" incoming nerves to the muscle fiber; thought to signal to induce neurite outgrowth
CALPAIN
enzymes that are activated when calcium levels rise too high; cause regeneration
calcineurin/NFAT
this pathway is the activity-dependent transformation of fast fibers into slow fibers
epithelial
these types of cells form a continuous layer that line the surfaces of organs; form a selective permeability layer, secrete substances, and protect from danage
unilaminar
epithelial cells that form a single layer in adjacent tissues (squamous, cuboidal)
multilaminar
epithelial cells that form multiple layers (stratified squamous, stratified cuboidal or columnar)
exocrine
glands that secrete onto external surfaces through ducts
endocrine
glands that are ductless and secrete messengers into the blood (insulin)
paracrine
glands that secrete substances into the extracellular fluid compartment
special skeletal
this type of connective tissue consists of cartilage and bone and includes chondrocytes, osteocytes, osteoblasts, and osteoclasts; they are found embedded in a matrix that they secrete
general type
the type of connective tissues that are subdivided into resident and transient immigration cells
resident
cells of the general type of connective tissues that stay fixed in location and include fibroblasts, adipocytes, macrophages, pericytes, and mast cells
transient
these types of general type of connective tissues originate in the bone marrow and circulate int he bloodstream, then leave the circulation and enter the connective tissue to perform their specific function; are B and T lymphocytes, plasma cells, neutrophils, eosinophils, basophils, monocytes, and macrophages
collagen and elastin
these are the insoluble protein fibrils of the extracellular matrix
collagen
a structural protein that is about 30% of the body's proteins; there are many types and contain hydroxyproline and three polypeptides arranged in helices
elastin
these fibers are synthesized by fibroblasts and smooth muscle cells; they stretch easily with near perfect recoil, but calcify with age; surrounded by a sheath of microfibrils and are responsible for the elasticity of connective tissue
soluble polymers
ground substance of the ECM; hydrated gel like material that absorbs compressive forces and composed of three families of macromolecules
glycosaminoglycans (GAG)
these proteins are negatively charged chains of repeating disaccharide units that possess high osmotic activity and are therefore capable of binding large amounts of water; they resist compression forces
proteoglycans
sulfated GAGs that form covalent bonds with a protein core; located in the ground substance of the ECM and they resist compression, retard microorganisms, form molecular filters, possess binding sites for signaling molecules and function as cytoskeletal components
cell adhesive glycoproteins
located in the ground substance of the ECM; allow for cells to adhere to the components of the ECM
fibronectin
type of glycoprotein that is synthesized by fibroblasts and act as guidance pathways for the embryonic cells and also function in wound repair
laminin
a glycoprotein that is found in the basal lamina and binds with type IV collagen and the cell membrane
tenascin
a glycoprotein that is limited to embryonic tissue where it functions as a migratory path for cell migrations and axon growth
basal lamina
consists of two layers, the lamina lucida and the lamina densa
lamina lucida
this layer of the basal lamina consists of the extracellular glycoproteins and transmembrane glycoproteins
lamina densa
this layer of the basal lamina is made up of a meshwork of type IV collagen
lamina reticularis
this layer is made up of type I, III, and VII collagen, and it serves as an interface between the basal lamina and the connective tissues
glycocalyx
this is a cell coat that consists of glycoproteins and glycolipids that form an integral part of the plasma membrane; cell antigens may be found here and also specialized adhesion molecules
tight junctions
these types of junctions regulate the passage of molecules between cells
gap
these types of junctions allow for communication between adjacent cells
demosomes
these types of junctions function to hold adjacent cells firmly together in areas of mechanical stress
adherence
these types of junctions link actin fibers between adjacent cells
cell matrix
these types of junctions anchor cytoskeletal proteins to ECM macromolecules
focal adhesions
these junctions link intracellular actin fibers to ECM proteins
hemidesmosome
these junctions link intracellular cytoskeletal proteins to ECM proteins
homeostasis
constancy of the internal environment
2/3
intracellular fluid represents ___ of total body water
1/3
extracelllular fluid represents ___ of total body water and is composed of two volumes of fluid
interstitial fluid
one component of extracellular fluid that is 80%
plasma volume
one component of extracellular fluid that is 20%
40-70%
TBW comprises __ to __ % of total body mass
fibroblasts
a type of resident cell that is flattened and irregular with branching processes; it synthesizes most of the ECM of the connective tissue, therefore are highly active; they adhere to collagen and elastin and play a major role in wound repair
adipocytes
function in synthesis, storage, and release of fat from glycerol, fatty acids, and glucose; synthesize and secrete a number of chemical messengers and are now considered to be a major endocrine organ
macrophages
resident cells that functions as phagocytes (eliminate foreign substances by engulfing them); play many important roles in inflammation (synthesize and secrete cytokines)
pericytes
resident cells that surround the endothelial cells of capillaries;they share the basal lamina of endothelial cells and may undergo differentiation to become smooth muscle cells and endothelial cells in the walls
mast cells
these cells are derived from bone marrow cells, and function in mediation inflammation; they are the largest of fixed connective tissue cells, and secrete many substances
excitability, elasticity, contractility, relaxation
the four differentiated functions of muscle cells
satellite
these cells are located out of the plasma membrane but within/below the basal lamina; they are stem cells and are the sole source of postnatal myonuclei
3-10%
satellite cells represent between __ and __ of all muscle nuclei
sarcolemma
this skeletal muscle membrane includes both the basal lamina and the plasma membrane
myoplasticity
the capacity of muscle for adaptive change
sugar, phosphoric acid, nitrogen base
the three components of nucleotides
mRNA
RNA that encodes the protein
rRNA
RNA part of the ribosome that is used to translate mRNA into a protein
tRNA
RNA that couples the region which binds the mRNA codon and its amino acid; transports the protein coded on mRNA
transcription
the process of making an RNA copy of a single gene
RNA polymerase
the enzyme that aids in transcription
5-3
the direction in which transcription occurs down the DNA molecule
exons
the parts of the mRNA copy that will be expressed
introns
the parts of the mRNA copy that will be snipped out and not expressed
translation
the process of reading the RNA sequence of an mRNA and creating the amino acid sequence of a protein
64, 20
there are __ possible codons that code for __ different amino acids in the body
AUG, methionine
the start codon in translation is __, which codes for the protein __
N terminal
the location on the first amino acid of a protein that contains a free amino group
C terminal
the location on the last amino acid of a protein that has a free acid group
3'
the amino acid on the tRNA is attached to the __ end
aminoacyl tRNA synthetases
enzymes used to charge the tRNA with the proper amino acid
release factors
during translation, these proteins bind to the stop codon, causing the ribosome, the mRNA , and the new polypeptide to separate
polypeptides
linear chains of amino acids
primary structure
the sequence of amino acids in a polypeptide is known as its __ structure
peptide
the bonds that are formed between the acid group of one protein and the amino group of the other protein
secondary
this structure is a conformation of a short peptide, mainly determined by hydrogen bonds (alpha helix and beta pleated sheets)
tertiary
this protein structure is the conformation of a whole polypeptide chain
slow twitch (type I)
these types of fibers have a slow contraction time, are highly resistant to fatigue, smaller, have high mitochondrial and myoglobin density, high levels of oxidative enzymes and low levels of glycolysis
FOG (Type IIA)
these types of fibers are moderate in resistance to fatigue and have high mitochondrial density; they are high in creatine phosphate and glycogen, and have high glycolytic and oxidative enzyme activity
FG (Type IIB)
these types of fibers are sensitive to fatigue and are short anaerobic fibers; they are large and have low mitochondrial density and myoglobin; high in creatine phosphate and glycogen, so high glycolytic enzyme content and low oxidative content
fast
the SR and T-system occupies 2-3 times more volume in __ fibers
intrafusal
these types of fibers are part of the muscle spindle and are innervated by gamma motor neurons; they are proprioceptive in nature
extrafusal
these types of fibers are innervated by alpha motor neurons and contract, generating skeletal movement
PEVK
this region in titin is the spring-like elastic element
nicotinic
the receptor on the postsynaptic terminal for ACh is a __ type or receptor
myopathy
a variation in fiber type size (degeneration and regeneration of muscle fibers)
dystrophy
replacement of muscle fibers with increased connective tissue
atrophy
the active process of increase in protein degradation and a decrease in protein synthesis
endurance
__ training leads to more type I fibers
strength
__ training leads to more type II fibers
type II
type __ fibers are selectively atrophied during disuse
cachexia
a wasting syndrome that is a loss of weight, muscle atrophy, fatigue, weakness, and significant loss of appetite in someone who is not trying to lose weight; basically a loss of body mass that cannot be reversed nutritionally
tumor necrosis factor a, or cachexin
thought to be the most likely mediator of cachexia
sarcopenia
muscle weakness and wasting in the elderly possibly due to a decrease in the proliferative capacity or number of satellite cells or accumulating mitochondrial DNA deletion
critical illness myopathy
muscle weakness that is prevalent in patients receiving intensive care during a critical illness; hallmark is loss of myosin
7-10
half life of muscle structural proteins is __-__ days
days or hours
the time course of atrophy is __ or __
days
the time course of hypertrophy is __
FOXO
these proteins induce the ubiquitin ligase pathway and cause muscle atrophy
ubiquitin ligase
the pathway for muscle atrophy that is caused by an attachment of ubiquitin and lysine, targeting specific protein substrates for degradation
myostatin
a signaling molecule that is secreted by muscle and negatively regulates muscle mass; it is thought to regulate the proliferation of muscle stem cells and decreases satellite cell incorporation and myoblast differentiation; it also inhibits Akt protein synthesis