(Downloading may take up to 30 seconds.
If the slide opens in your browser, select File -> Save As to save it.)



Fig. 4. A hypothetical molecular model depicting the segregation of focal contacts and fibrillar adhesions. (A) Initial adhesions contain both {alpha}5ß1 integrin (bound primarily to fibronectin) and {alpha}vß3 integrin (bound primarily to vitronectin). Both integrins are associated through different proteins with actin filaments and are subjected to actomyosin-driven contraction forces. (B) Since substrate-attached vitronectin forms a rigid matrix, {alpha}vß3 integrin remains immobile despite the applied contraction force. In contrast, {alpha}5ß1 integrin is bound to a relatively soft fibronectin matrix and thus translocates centripetally owing to the actomyosin-driven pulling. The translocation of the fibronectin receptor can also stretch the fibronectin matrix and promote fibrillogenesis. Abbreviations: a, actin; {alpha}, {alpha}-actinin, F, FAK; fn, fibronectin; m, myosin II; P, parvin/actopaxin; pa, paxillin; ta, talin; te, tensin; vi, vinculin; vn, vitronectin; 51, {alpha}5ß1 integrin; v3, {alpha}vß3 integrin.