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19 Cards in this Set

  • Front
  • Back
fibronectin: binding domain and location
-binds to integrins, collagen, heparin, heparan sulfate, and hyaluronic acid
-connective tissue, blood plasma and embryonic tissue
laminin: binding domain and location
-integrins, heparan sulfate, collagen IV and enactin
-basal lamina
nidogen (enactin): binding domain and location
-laminin and type IV collagen
-basal lamina
tenascin: binding domain and location
-syndecans and fibronecting
-embryonic tissue
chondronectin: binding domain and location
-collagen II, chondroitin sulfates, hyaluronic acid, and integrins of chondrocytes
-cartilage
osteonectin: binding domain and location
-collagen I, proteoglycans, and integrins of bone cells (osteocytes and osteoblasts)
-bone
Type I collagen tissue distribution
-dermis, tendon, bone, dentin, cementum, fibrocartilage, organ capsules
Type II collagen tissue distribution
-hyaline and elastic cartilage
Type III collagen tissue distribution
-spleen, liver, lymph nodes, skin, lungs, smooth muscle
Type IV collagen tissue distribution
-basal lamina
type V collagen tissue distribution
dermis, tendon, bone, fibrocartilage
type VII collagen distribution
dermis
Ehlers-Danlos type IV: defect and clinical consequence
-COL3A1 encoding type III (reticular fibers)
-varicose veins, aortic rupture, intestinal rupture
Ehlers-Danlos type VI: defect and clinical consequence
-hydroxylation of lysine, destabilizes collagen
-hyperelasticity of skin, rupture of eyeball
Ehlers-Danlos type VII: defect and clinical consequence
-COL1A1 and COL1A2 encoding type I collagen
-joint dislocation and hypermobility of joints
scurvey: defect and clinical consequence
-tropocollagen molecules cannot aggregate into fibrils due to decreases hydroxylation of proline
-gum ulceration and hemorrhages
osteogenesis imperfecta: defect and clinical consequence
-COL1A1, reduced synthesis of type I collagen
-spontaneous fractures and cardiac insufficiency
strickler syndrome: defect and clinical consequence
-COL2A1, type II collagen
-myopia, hypoplasia of mandible, arthritis
marfan syndrome: defect and clinical consequence
-fibrillin 1
-aortic aneurysm or rupture, myopia, detached lens, skeleton defects