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Dynamic actin cycling through mitochondrial subpopulations locally regulates the fission–fusion balance within mitochondrial networks

机译:通过线粒体亚群的动态肌动蛋白循环局部调节线粒体网络内的裂变-融合平衡

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摘要

Mitochondria form interconnected networks that dynamically remodel in response to cellular needs. Using live-cell imaging, we investigate the role of the actin cytoskeleton in regulating mitochondrial fission and fusion. We identify cycling of actin filaments onto and off of subsets of cellular mitochondria. The association of actin filaments with mitochondrial subpopulations is transient; actin quickly disassembles, then reassembles around a distinct subpopulation, efficiently cycling through all cellular mitochondria within 14 min. The focal assembly of actin induces local, Drp1-dependent fragmentation of the mitochondrial network. On actin disassembly, fragmented mitochondria undergo rapid fusion, leading to regional recovery of the tubular mitochondrial network. Cycling requires dynamic actin polymerization and is blocked by inhibitors of both Arp2/3 and formins. We propose that cyclic assembly of actin onto mitochondria modulates the fission/fusion balance, promotes network remodelling and content mixing, and thus may serve as an essential mechanism regulating mitochondrial network homeostasis.
机译:线粒体形成相互连接的网络,这些网络可以根据细胞的需要动态地进行重塑。使用活细胞成像,我们调查肌动蛋白细胞骨架在调节线粒体裂变和融合中的作用。我们确定肌动蛋白丝循环到细胞线粒体的子集中。肌动蛋白丝与线粒体亚群的关联是短暂的;肌动蛋白迅速分解,然后在不同的亚群周围重新组装,可在14分钟内有效循环遍及所有细胞线粒体。肌动蛋白的局灶性组装诱导线粒体网络局部依赖Drp1的片段化。肌动蛋白拆卸时,破碎的线粒体会快速融合,从而导致管状线粒体网络区域性恢复。循环需要动态的肌动蛋白聚合,并被Arp2 / 3和formins的抑制剂阻断。我们提出肌动蛋白在线粒体上的周期性装配可调节裂变/融合平衡,促进网络重塑和内容混合,因此可作为调节线粒体网络稳态的重要机制。

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