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Microfilament-organizing centers in areas of cell contact: cytoskeletal interactions during cell attachment and locomotion

机译:细胞接触领域的微丝组织中心: 细胞附着和运动过程中的细胞骨架相互作用

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摘要

In this article we discuss three aspects of cell contact formation: (a) the molecular architecture of the cytomatrix in cell-to-substrate focal contacts, (b) the dynamic properties of membrane- and microfilament-associated proteins in the contact areas, and (c) the involvement of microtubules in the coordinated and directed formation of new substrate contacts during cell locomotion. We show that different microfilament-associated proteins exhibit distinct patterns of association with focal contacts: some proteins are specifically associated with focal contacts (vinculin and talin); alpha-actinin is enriched in the contact areas but also is present along the stress fibers and in the lamellipodium; actin and filamin are detected throughout the contact areas but in apparently reduced amounts compared with the associated stress fibers; and tropomyosin, myosin, and spectrin are either absent from the endofacial surfaces of contact areas or are present in only very small amounts. Fluorescence photobleaching recovery analyses performed with living cells microinjected with fluorescently labeled actin, vinculin, and alpha-actinin indicate that each of these proteins maintains a dynamic equilibrium between a soluble cytoplasmic pool and a membrane-bound fraction. Correlation of the distribution of vinculin and tubulin in motile fibroblasts to local movements of the leading edge of the same cells indicates that free-end microtubules extend into actively ruffling areas along the lamellipodium and that new vinculin-containing contacts are preferentially formed in these protruding regions.
机译:在本文中,我们讨论了细胞接触形成的三个方面:(a)细胞与底物焦点接触中细胞基质的分子结构,(b)接触区域中与膜和微丝相关的蛋白质的动态特性,以及(c)在细胞运动过程中微管参与新的底物接触的协调和定向形成。我们表明,不同的微丝相关蛋白表现出与焦点接触不同的模式:一些蛋白质与焦点接触(vinculin和塔林)专门相关; α-肌动蛋白在接触区域富集,但在应力纤维和层状脂蛋白中也存在。在整个接触区域都检测到了肌动蛋白和纤维蛋白,但与相关的应力纤维相比,其数量明显减少了;接触区域的内表面不存在原肌球蛋白,肌球蛋白和血影蛋白,或仅以极少量存在。用微注射了荧光标记的肌动蛋白,纽扣素和α-肌动蛋白的活细胞进行的荧光光漂白恢复分析表明,这些蛋白中的每一种都在可溶性细胞质池和膜结合级分之间保持动态平衡。运动型成纤维细胞中长春花素和微管蛋白的分布与同一细胞前缘的局部运动的相关性表明,自由端微管沿着板状脂质体延伸到活跃的起皱区,并且优先在这些突出区域中形成新的含长春花素的接触。

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