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培养的成肌细胞和成纤维细胞上细胞基质附着(CSAT)抗原的分布。

Distribution of the cell substratum attachment (CSAT) antigen on myogenic and fibroblastic cells in culture.

作者信息

Damsky C H, Knudsen K A, Bradley D, Buck C A, Horwitz A F

出版信息

J Cell Biol. 1985 May;100(5):1528-39. doi: 10.1083/jcb.100.5.1528.

Abstract

Previous studies (Neff et al., 1982, J. Cell. Biol. 95:654-666; Decker et al., 1984. J. Cell. Biol. 99:1388-1404) have described a monoclonal antibody (CSAT Mab) directed against a complex of three integral membrane glycoproteins of 120,000-160,000 mol wt (CSAT antigen [ag]) involved in the cell matrix adhesion of myoblasts and fibroblasts. In localization studies on fibroblasts presented here, CSAT ag has a discrete, well-organized distribution pattern. It co-aligns with portions of stress fibers and is enriched at the periphery of, but not directly beneath vinculin-rich focal contacts. In this last location, it co-distributes with fibronectin, consistent with the suggestion that the CSAT ag participates in the mechanism by which fibroblasts attach to fibronectin. In prefusion myoblasts, which are rapidly detached by CSAT Mab, CSAT ag is distributed diffusely as are vinculin, laminin, and fibronectin. After fusion, myotubes become more difficult to detach with CSAT Mab. The CSAT ag and vinculin are organized in a much more discrete pattern on the myotube surface, becoming enriched at microfilament bundle termini and in lateral lamellae which appear to attach myotubes to the substratum. These results suggest that the organization of CSAT ag-adhesive complexes on the surface of myogenic cells can affect the stability of their adhesive contacts. We conclude from the sum of the studies presented that, in both myogenic and fibroblastic cells, the CSAT ag is localized in sites expected of a surface membrane mediator of cell adhesion to extracelluon of CSAT ag-adhesive complexes on the surface of myogenic cells can affect the stability of their adhesive contacts. We conclude from the sum of the studies presented that, in both myogenic and fibroblastic cells, the CSAT ag is localized in sites expected of a surface membrane mediator of cell adhesion to extracellular matrix. The results from studies that use fibroblasts in particular suggest the involvement of CSAT ag in the adhesion of these cells to fibronectin.

摘要

先前的研究(Neff等人,1982年,《细胞生物学杂志》95:654 - 666;Decker等人,1984年,《细胞生物学杂志》99:1388 - 1404)描述了一种单克隆抗体(CSAT单克隆抗体),它针对的是一种由分子量为120,000 - 160,000的三种整合膜糖蛋白组成的复合物(CSAT抗原[ag]),该复合物参与成肌细胞和成纤维细胞与细胞基质的黏附。在此处展示的对成纤维细胞的定位研究中,CSAT抗原具有离散、组织良好的分布模式。它与应力纤维的部分区域共排列,并在富含纽蛋白的粘着斑的周边富集,但不在其正下方。在最后这个位置,它与纤连蛋白共分布,这与CSAT抗原参与成纤维细胞附着于纤连蛋白的机制这一观点一致。在预融合的成肌细胞中,CSAT单克隆抗体能使其迅速脱离,CSAT抗原与纽蛋白、层粘连蛋白和纤连蛋白一样呈弥散分布。融合后,肌管更难被CSAT单克隆抗体分离。CSAT抗原和纽蛋白在肌管表面以一种更加离散的模式组织起来,在微丝束末端和似乎将肌管附着于基质的侧板中富集。这些结果表明,成肌细胞表面CSAT抗原 - 黏附复合物的组织方式可影响其黏附接触的稳定性。我们从所呈现的研究总和中得出结论,在成肌细胞和成纤维细胞中,CSAT抗原定位于预期的细胞与细胞外基质黏附的表面膜介质所在的位置。特别是使用成纤维细胞的研究结果表明CSAT抗原参与了这些细胞与纤连蛋白的黏附。

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