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

机译:内质网的INF2介导的肌动蛋白聚合反应刺激线粒体钙的摄取内膜收缩和分裂

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摘要

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.
机译:线粒体分裂需要内部和外部线粒体膜(分别为IMM和OMM)分开。与内质网(ER)的相互作用通过招募动力Drp1促进OMM分裂,但对IMM分裂的影响尚不明确。我们以前表明肌动蛋白聚合反应通过ER结合倒立的形式2(INF2)刺激哺乳动物细胞中的Drp1募集。在这里,我们显示INF2介导的肌动蛋白聚合反应可刺激第二个线粒体反应,而独立于Drp1:线粒体钙单向转运体增加了线粒体基质钙。 ER储存增加了线粒体钙的含量,肌动蛋白的作用是增加ER与线粒体的接触。线粒体钙的增加也需要肌球蛋白IIA。升高的线粒体钙反过来以Drp1独立的方式激活IMM收缩。 IMM收缩需要电子传输链活性。 IMM划分先于OMM划分。这些结果表明,肌动蛋白聚合在线粒体分裂过程中独立地刺激两个膜的动力学:IMM通过增加基质钙,OMM通过Drp1募集。

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