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49 Cards in this Set
- Front
- Back
Intramembranous osteogenesis |
mesenchyme --> bone formation From from a membrane of mesenchymal cells (flat bones of the skull) Week 8 of development |
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Endochondral osteogenesis |
Cartilage --> bone occurs in long bones 1 form cartilage 2 form bone 3 remove cartialge |
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Intramembranous bone formation (week 8 of embryo) |
mesenchymal cells differentiate into osteoprogenitor cells (form bone blastema) express Runx2 then express Osx Bone is formed |
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Intramembranous: dense bones |
Forms haversian systems |
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Endochondral Bone formation |
All form from a hyaline cartilage template Bone of the extremities, vertebral column, pelvis |
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Metaphysis |
part of the diaphyses (shaft) that's closest to the epiphyses (end); bone at this part is particularly dense, known to have an epiphyseal growth plate and an epiphyseal line |
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Zones in epiphyseal cartilage |
Reserve zone: primitive hyaline cartilage responsible for the growth in length of bone Proliferative zone: has actively mitotic chondrocytes (make matrix proteins) Hypertrophic zone: apoptosis of chondrocytes and calcification of the territorial matrix |
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Indian headgehog (Ihh) |
stimulates chondrocyte proliferation (type II and XI collgen is made) by stimulating them to produce Runx2 and become osteoblasts of the bony collar & stimulates them to produce parathyroid hormone peptides (inhibits chondrocytes in the proliferating some from becoming hypertrophic & stimulates chondrocyte proliferation in the reserve zone) |
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Hypertrophic zone |
hypertrophied chondrocytes produce VEGF (important in vascularization), collage X, and then undergo apoptosis Just before the zone of vascular invasion |
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Vascular invasion zone |
Blood vessels bring in preosteoblasts and resporptive chondroclasts; preosteoblasts give rise to osteoblasts which start laying down osteoid.. bony spicules form |
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spicule |
calcified cartilage coated by osteoid |
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Trabecula |
core of lamellar bone with osteoblasts laying down osteoid |
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Hereditary bone disorders |
Albers-Schonberg Disease: abnormal osteoclast function (osteopetrosis) Fibrodysplasia ossificans progressiva: ectopic bone formation Osteogenesis imprefecta: fragile bones |
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Skeletal muscle |
Moves the skeleton and other structures such as precise eye movement |
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Cardiac muscle |
heart muscle; propels blood through the heart and lungs into aorta |
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Smooth muscle |
contraction of blood vessels, viscera, intrinsic muscle of the eye |
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Characteristic of skeletal muscle |
Striated; nuclei located at the periphery of the muscle; originates from ventral somite bodies in embryo |
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Differentiation of skeletal muscle |
Myoblasts fuse --> myocytes fuse --> to make myotubes --> muscle Myotubes cannot differentiate (terminally differentiated state) contractile proteins are made in the muscle cells and not elsewhere because of transactivators and transcription factors |
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MyoD |
in skeletal muscles: family of transactivating proteins (Basic loop helix region) |
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Skeletal muscle Hierarchy |
repeating Sarcomeres make up myofilaments which make up Myofibrils make up muscle fiber (wrapped in endomysium) Bunches of muscle fibers make up the fascicle ( fxnal unit of myofiber wrapped in perimysium) Fascicles make up the whole skeletal muscle (muscle wrapped in epimysium) (voluntary muscle) |
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A band |
dark band (thick filaments only) Myosin |
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I band |
Light band (thin filaments only) Actin |
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Z Disc |
Separates sarcomeres; attachment point for titian and thin filaments |
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M line |
thick accessory filaments linked by accessory proteins; houses creatine kinase (transfers phosphate ADP --> ATP) |
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Actin |
made up of G actin monomers which polymerize to form F-actin filament |
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Myosin |
made up of myosin light and heavy chains Head associated with MLC (myosin light chain), ATP ATPase anchored to z disc by titin hydrolyses ATP |
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Tropomyosin |
Double helix of two polypeptides lies in the groove between actin molecules |
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Thin Actin filament unit |
TnT: binds tropomyosin TnI: inhibits the binding of myosin to actin TnC: binds calcium Troponin: three globular subunits anchored to z line by alpha- actinin capped by tropomodulin (regulates length of actin filament) stabilized by nebulin |
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Neuromuscular spindle |
Detects passive stretch Intrafusal fibers: made up of chain fibers (sustained stretch) and bag fibers (onset of stretch) ; sensory receptor; associated with sensory neurons; Extrafusal fibers: cause the contraction of the muscle |
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Satellite cells |
Skeletal muscle does not divide after it's been damaged; instead satellite cells are adult stem cells that will proliferate and turn into skeletal muscle |
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Purkinje cells |
conduction tissue of the heart |
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Smooth muscle |
does not have neural input; no precise neural control; cells interact via gap jxns; enclosed in reticular fibers and basal lamina; can divide when terminally differentiated |
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Neuepithelial cells... |
give rise to gliablasts. These differentiate into oligodendroglia, fibrillar astrocyte, and protoplasmic astrocytes (supportive cells of the nervous system) also gives rise to neuroblasts which will become neurons |
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Mantle layer (formed from neuroepithelial cell migration) |
forms the Gray matter |
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PAX3 |
Increase in this leads to specification of ectoderm cells into neural crest cells |
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SOX10 |
involved in the differentiation of the neural crest cells |
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Neural crest cells form... |
sensory neurons, parasympathetic and sympathetic autonomic ganglia |
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Neural tube cells form... |
somatic efferent neurons, preganglionic sympathetic and parasympathetic neurons |
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In maternal diabetes.. |
elevated glucose levels leads to an decline in Pax3 |
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Paraxial mesoderm gives rise to... |
somites which gives rise to skeletal muscle
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Splanchnic mesoderm gives to... |
cardiac and smooth muscle |
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Multipotent stem cell + Notch = |
smooth muscle |
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Multipotent stem cell + BMP = |
endothelium |
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Multipotent stem cell + Prdm16 = |
Brown fat |
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Multipotent stem cell + high Shh = |
cartilage |
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Multipotent stem cell + WNT = |
skeletal muscle |
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Multipotent stem cell + BMP2/TGFbeta Menin = |
bone |
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Myogenic progenitor + MyoD ... |
allows of specialization of myofibre
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Neuromuscular dystrophy |
absence of dystrophin (stabilizes the sarcomere during a muscle contraction), without dystrophin the DAP complex is lost |