Suppr超能文献

非肌肉肌球蛋白-II是为后续分裂产生缢缩位点所必需的。

Non-muscle Myosin-II Is Required for the Generation of a Constriction Site for Subsequent Abscission.

作者信息

Wang Kangji, Wloka Carsten, Bi Erfei

机构信息

Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6058, USA.

Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6058, USA; Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, 9747 AE Groningen, the Netherlands.

出版信息

iScience. 2019 Mar 29;13:69-81. doi: 10.1016/j.isci.2019.02.010. Epub 2019 Feb 18.

Abstract

It remains unknown when, where, and how the site of abscission is generated during cytokinesis. Here, we show that the sites of constriction, i.e., the sites of future abscission, are initially formed at the ends of the intercellular bridge during early midbody stage, and that these sites are associated with the non-muscle myosin-IIB (not myosin-IIA), actin filaments, and septin 9 until abscission. The ESCRT-III component CHMP4B localizes to the midbody and "spreads" to the site of abscission only during late midbody stage. Strikingly, inhibition of myosin-II motor activity by a low dose of Blebbistatin completely abolishes the formation of the constriction sites, resulting in the localization of all the above-mentioned components to the midbody region. These data strongly suggest that a secondary actomyosin ring provides the primary driving force for the thinning of the intercellular bridge to allow ESCRT-mediated membrane fission.

摘要

胞质分裂过程中,脱落位点何时、何地以及如何产生仍然未知。在这里,我们表明,缢缩位点,即未来的脱落位点,最初在中体早期的细胞间桥末端形成,并且这些位点在脱落之前与非肌肉肌球蛋白-IIB(而非肌球蛋白-IIA)、肌动蛋白丝和septin 9相关联。ESCRT-III组分CHMP4B仅在中体后期定位于中体并“扩展”到脱落位点。引人注目的是,低剂量的Blebbistatin抑制肌球蛋白-II的运动活性会完全消除缢缩位点的形成,导致上述所有组分定位于中体区域。这些数据有力地表明,次生肌动球蛋白环为细胞间桥的变薄提供了主要驱动力,以允许ESCRT介导的膜裂变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc32/6396101/d4cc386d67ab/fx1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验