Borg5/Cdc42EP1 限制了上皮 MDCK 细胞的收缩性和运动性。

IF 3.3 3区 生物学 Q3 CELL BIOLOGY
David Cohen, Dawn Fernandez, Francisco Lázaro-Diéguez, Beatrix Überheide, Anne Müsch
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引用次数: 0

摘要

Borg/Cdc42EP 家族由 septin 结合蛋白组成,已知它们能促进依赖 septin 的应力纤维和肌动蛋白收缩性。我们在此表明,上皮细胞 Borg5/Cdc42ep1 反而限制了收缩性、细胞-细胞粘附张力和运动性,这是在成熟的 MDCK 单层中获得柱状、各向同性细胞形态所必需的。Borg5 的耗竭抑制了横向 F-肌动蛋白皮层的发育,刺激了微管依赖的前缘片层以及径向应力纤维,而且与基底 F-肌动蛋白表型无关,导致了压实单层细胞顶端表面的各向异性。我们确定,Borg5 限制了septin与微管的定位,而且与septin 2一样,Borg5也与肌球蛋白- IIA的杆域相互作用。在有隔蛋白存在的情况下,肌球蛋白-IIA与Borg5的相互作用减弱。由于隔蛋白也介导肌球蛋白活化,我们认为 Borg5 限制了 MDCK 细胞的收缩能力,部分原因是抵消了隔蛋白相关的肌球蛋白活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Borg5/Cdc42EP1 restricts contractility and motility in epithelial MDCK cells.

The Borg/Cdc42EP family comprises septin binding proteins, which are known to promote septin-dependent stress fibers and acto-myosin contractility. We show here that epithelial Borg5/Cdc42ep1 instead limits contractility, cell-cell adhesion tension and motility as is required for the acquisition of columnar, isotropic cell morphology in mature MDCK monolayers. Borg5 depletion inhibited the development of the lateral F-actin cortex, stimulated microtubule-dependent leading-edge lamellae as well as radial stress fibers and, independently of the basal F-actin phenotype, caused anisotropy of apical surfaces within compacted monolayers. We determined that Borg5 limits septin-colocalization with microtubules, and that like Septin 2, Borg5 interacts with the rod-domain of Myosin- IIA. The interaction of Myosin-IIA with Borg5 was reduced in the presence of septins. Because septins also mediate myosin activation, we propose that Borg5 limits contractility in MDCK cells in part by counteracting septin-associated myosin activity.

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来源期刊
Journal of cell science
Journal of cell science 生物-细胞生物学
CiteScore
7.30
自引率
2.50%
发文量
393
审稿时长
1.4 months
期刊介绍: Journal of Cell Science publishes cutting-edge science, encompassing all aspects of cell biology.
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