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Fig. 4. Thrombin cleavage of G4/5 inhibits deposition of pre-lam5 by {alpha}3–/– MKs. {alpha}3–/– MKs attached to glass coverslips were incubated (overnight) with either culture media alone (A; a-c), media with heparin-purified lam5 (A; d-f) or heparin-purified lam5 that has been digested with thrombin (A; g-i). The coverslips were processed for immunofluorescence to visualize ECM deposits containing the human {gamma}2 chain (a,d,g; B4-6), {alpha}3 chain (b,e,h; C2-5) or the G4/5 domains of {alpha}3200 (c,f,i; D2-1). Deposition occurred only where lam5 containing {alpha}3200 (C; lane 1) was added, and was prevented by thrombin digestion of the {alpha}3200 to {alpha}3165 (C, lane 2). Bar in (f), 20 µm. (B) Quantitation of deposit area/cell for six random fields for each of the conditions in A. (C) Western blot of lam5 preparations used in A and B. Lane 1, heparin-purified lam5; lane 2, heparin-purified lam5 from lane 1, digested with thrombin.





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