Department of Cell Biology, University College London, Institute of Ophthalmology, London, United Kingdom.
PLoS One. 2013;8(1):e53774. doi: 10.1371/journal.pone.0053774. Epub 2013 Jan 14.
Mitochondrial homeostasis is critical in meeting cellular energy demands, shaping calcium signals and determining susceptibility to apoptosis. Here we report a role for anxA6 in the regulation of mitochondrial morphogenesis, and show that in cells lacking anxA6 mitochondria are fragmented, respiration is impaired and mitochondrial membrane potential is reduced. In fibroblasts from AnxA6(-/-) mice, mitochondrial Ca(2+) uptake is reduced and cytosolic Ca(2+) transients are elevated. These observations led us to investigate possible interactions between anxA6 and proteins with roles in mitochondrial fusion and fission. We found that anxA6 associates with Drp1 and that mitochondrial fragmentation in AnxA6(-/-) fibroblasts was prevented by the Drp1 inhibitor mdivi-1. In normal cells elevation of intracellular Ca(2+) disrupted the interaction between anxA6 and Drp1, displacing anxA6 to the plasma membrane and promoting mitochondrial fission. Our results suggest that anxA6 inhibits Drp1 activity, and that Ca(2+)-binding to anxA6 relieves this inhibition to permit Drp1-mediated mitochondrial fission.
线粒体动态平衡对于满足细胞能量需求、塑造钙信号以及决定细胞对细胞凋亡的易感性至关重要。在这里,我们报告了 anxA6 在调节线粒体形态发生中的作用,并表明在 anxA6 缺失的细胞中,线粒体碎片化,呼吸受损,线粒体膜电位降低。在 AnxA6(-/-) 小鼠的成纤维细胞中,线粒体 Ca(2+)摄取减少,细胞浆 Ca(2+)瞬变升高。这些观察结果促使我们研究 anxA6 与参与线粒体融合和裂变的蛋白质之间可能存在的相互作用。我们发现 anxA6 与 Drp1 相关联,并且 Drp1 抑制剂 mdivi-1 可以预防 AnxA6(-/-)成纤维细胞中的线粒体碎片化。在正常细胞中,细胞内 Ca(2+)的升高破坏了 anxA6 和 Drp1 之间的相互作用,将 anxA6 移位到质膜并促进线粒体裂变。我们的结果表明 anxA6 抑制 Drp1 活性,而 anxA6 与 Ca(2+)的结合可以解除这种抑制,从而允许 Drp1 介导的线粒体裂变。