INF2 介导线粒体 ER 上的肌动蛋白聚合,刺激线粒体钙摄取、内膜收缩和分裂。

INF2-mediated actin polymerization at the ER stimulates mitochondrial calcium uptake, inner membrane constriction, and division.

机构信息

Department of Biochemistry and Cell Biology, Geisel School of Medicine at Dartmouth, Hanover, NH.

Department of Biochemistry, Weill Cornell Medical College, New York, NY.

出版信息

J Cell Biol. 2018 Jan 2;217(1):251-268. doi: 10.1083/jcb.201709111. Epub 2017 Nov 15.

Abstract

Mitochondrial division requires division of both the inner and outer mitochondrial membranes (IMM and OMM, respectively). Interaction with endoplasmic reticulum (ER) promotes OMM division by recruitment of the dynamin Drp1, but effects on IMM division are not well characterized. We previously showed that actin polymerization through ER-bound inverted formin 2 (INF2) stimulates Drp1 recruitment in mammalian cells. Here, we show that INF2-mediated actin polymerization stimulates a second mitochondrial response independent of Drp1: a rise in mitochondrial matrix calcium through the mitochondrial calcium uniporter. ER stores supply the increased mitochondrial calcium, and the role of actin is to increase ER-mitochondria contact. Myosin IIA is also required for this mitochondrial calcium increase. Elevated mitochondrial calcium in turn activates IMM constriction in a Drp1-independent manner. IMM constriction requires electron transport chain activity. IMM division precedes OMM division. These results demonstrate that actin polymerization independently stimulates the dynamics of both membranes during mitochondrial division: IMM through increased matrix calcium, and OMM through Drp1 recruitment.

摘要

线粒体分裂需要内外两层线粒体膜(分别为 IMM 和 OMM)的分裂。与内质网(ER)的相互作用通过招募动力蛋白 Drp1 促进 OMM 的分裂,但对 IMM 分裂的影响尚未得到很好的描述。我们之前曾表明,通过 ER 结合的反向formin 2(INF2)进行肌动蛋白聚合会刺激哺乳动物细胞中 Drp1 的募集。在这里,我们表明,INF2 介导的肌动蛋白聚合会刺激第二个独立于 Drp1 的线粒体反应:通过线粒体钙单向转运体使线粒体基质钙升高。ER 储存提供增加的线粒体钙,肌动蛋白的作用是增加 ER-线粒体接触。肌球蛋白 IIA 也需要这种线粒体钙的增加。线粒体钙的升高反过来以 Drp1 独立的方式激活 IMM 收缩。IMM 收缩需要电子传递链的活性。IMM 分裂先于 OMM 分裂。这些结果表明,肌动蛋白聚合在独立地刺激线粒体分裂过程中两层膜的动力学:通过增加基质钙来调节 IMM,通过招募 Drp1 来调节 OMM。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce0f/5748994/02b0fa09617f/JCB_201709111_Fig1.jpg

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