Sechler J L, Schwarzbauer J E
Department of Molecular Biology, Princeton University, NJ 08544-1014, USA.
Cell Adhes Commun. 1997 Mar;4(6):413-24. doi: 10.3109/15419069709004458.
Assembly of a fibronectin (FN) matrix is a multistep process which influences a number of cellular functions including intracellular cytoskeletal organization and signaling responses. We have previously reported on a recombinant FN (recFN), FN delta III1-7, which differs from native FN in its rate of fibril formation. To determine the intracellular consequences of a delay in assembly, we compared the distribution of cytoskeletal proteins during the formation of native and recFN matrices by immunofluorescence at various time points. CHO alpha 5 cell cytoskeleton was reorganized in response to both native and recFN matrix formation. Assembly of native FN induced a rapid reorganization of actin into stress fibers and colocalization of alpha 5 beta 1 integrin, focal adhesion kinase (FAK), vinculin, and paxillin to regions of cell-matrix contact. alpha 5 beta 1 integrins and FAK are also clustered upon binding of FN delta III1-7 to cells but actin reorganization and focal adhesion formation are delayed and appear to be dependent on the formation of FN delta III1-7 fibrils. These results suggest that the structural framework of the matrix plays an important role in the ability of FN to initiate intracellular responses.
纤连蛋白(FN)基质的组装是一个多步骤过程,它会影响许多细胞功能,包括细胞内细胞骨架组织和信号反应。我们之前报道过一种重组FN(recFN),即FN delta III1-7,其原纤维形成速率与天然FN不同。为了确定组装延迟的细胞内后果,我们在不同时间点通过免疫荧光比较了天然和recFN基质形成过程中细胞骨架蛋白的分布。CHO α5细胞的细胞骨架会因天然和recFN基质的形成而发生重组。天然FN的组装诱导肌动蛋白迅速重排形成应力纤维,并且α5β1整合素、粘着斑激酶(FAK)、纽蛋白和桩蛋白共定位于细胞-基质接触区域。当FN delta III1-7与细胞结合时,α5β1整合素和FAK也会聚集,但肌动蛋白重排和粘着斑形成会延迟,并且似乎依赖于FN delta III1-7原纤维的形成。这些结果表明,基质的结构框架在FN引发细胞内反应的能力中起着重要作用。