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驱动蛋白相关运输参与细胞黏附的调节。

Kinesin-associated transport is involved in the regulation of cell adhesion.

作者信息

Kaverina I N, Minin A A, Gyoeva F K, Vasiliev J M

机构信息

Cancer Research Center, Russian Academy of Medical Sciences, Moscow, Russia.

出版信息

Cell Biol Int. 1997 Apr;21(4):229-36. doi: 10.1006/cbir.1997.0136.

Abstract

It has been recently shown that deploymerization of microtubules induces the elongation of focal contacts at the leading edge. On the other hand, cell shape and pseudopodial activity were found to depend on the microtubule-based motor kinesin. In this paper, we examine whether kinesin is involved in controlling the dynamics of adhesive structures at the cell surface. Microinjection of an antiblocking kinesin activity in vitro causes focal contact elongation similar to the effect of microtubule-depolymerizing drugs. Thus, the role of microtubules in cell adhesion lies in the supporting kinesin-based transport to the adhesion sites.

摘要

最近研究表明,微管的解聚诱导了前缘粘着斑的延长。另一方面,发现细胞形状和伪足活动依赖于基于微管的驱动蛋白。在本文中,我们研究驱动蛋白是否参与控制细胞表面粘着结构的动态变化。在体外显微注射抗阻碍驱动蛋白活性物质会导致粘着斑延长,类似于微管解聚药物的作用。因此,微管在细胞粘附中的作用在于支持基于驱动蛋白的向粘附位点的运输。

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