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细胞分裂期胞质分裂:磷酸肌醇和内体分选转运复合体引导最终切割。

Cytokinetic Abscission: Phosphoinositides and ESCRTs Direct the Final Cut.

作者信息

Gulluni Federico, Martini Miriam, Hirsch Emilio

机构信息

Department of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy.

出版信息

J Cell Biochem. 2017 Nov;118(11):3561-3568. doi: 10.1002/jcb.26066. Epub 2017 May 30.

Abstract

Cytokinetic abscission involves the fine and regulated recruitment of membrane remodeling proteins that participate in the abscission of the intracellular bridge that connects the two dividing cells. This essential process is mediated by the concomitant activity of the endosomal sorting complex required for transport (ESCRT) and the vesicular trafficking directed to the midbody. Phosphoinositides (PtdIns), produced at plasma membrane, and endosomes, act as molecular intermediates by recruiting effector proteins involved in multiple cellular processes, such as intracellular signaling, endo- and exo-cytosis, and membrane remodeling events. Emerging evidences suggest that PtdIns have an active role in recruiting key elements that control the stability and the remodeling of the cytoskeleton from the furrow ingression to the abscission, at the end of cytokinesis. Accordingly, a possible concomitant and coordinated activity between PtdIns production and ESCRT machinery assembly could also exist and recent findings are pointing the attention on poorly understood ESCRT subunits potentially able to associate with PtdIns rich membranes. Although further studies are required to link PtdIns to ESCRT machinery during abscission, this might represent a promising field of study. J. Cell. Biochem. 118: 3561-3568, 2017. © 2017 Wiley Periodicals, Inc.

摘要

细胞分裂期胞质分裂涉及膜重塑蛋白的精细且受调控的募集,这些蛋白参与连接两个正在分裂细胞的细胞内桥的分裂过程。这一关键过程由运输所需的内体分选复合体(ESCRT)的协同活性以及指向中间体的囊泡运输介导。在质膜和内体上产生的磷酸肌醇(PtdIns),通过募集参与多种细胞过程(如细胞内信号传导、胞吞和胞吐作用以及膜重塑事件)的效应蛋白,充当分子中间体。新出现的证据表明,在胞质分裂末期,从沟的侵入到分裂,PtdIns在募集控制细胞骨架稳定性和重塑的关键元件方面发挥着积极作用。因此,PtdIns产生与ESCRT机制组装之间可能也存在伴随且协调的活性,最近的研究结果将注意力指向了对潜在能够与富含PtdIns的膜结合的ESCRT亚基的了解不足。尽管在分裂过程中将PtdIns与ESCRT机制联系起来还需要进一步研究,但这可能代表一个有前景的研究领域。《细胞生物化学杂志》118: 3561 - 3568, 2017。© 2017威利期刊公司。

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