Université de Toulouse, UPS, CNRS, UMR 52412, Laboratoire Métabolisme Plasticité Mitochondries, Toulouse, France.
Semin Cell Dev Biol. 2010 Aug;21(6):593-8. doi: 10.1016/j.semcdb.2009.12.012. Epub 2010 Jan 4.
Mitochondrial morphology varies according to cell type and cellular context from an interconnected filamentous network to isolated dots. This morphological plasticity depends on mitochondrial dynamics, a balance between antagonistic forces of fission and fusion. DRP1 and FIS1 control mitochondrial outer membrane fission and Mitofusins its fusion. This review focuses on OPA1, one of the few known actors of inner membrane dynamics, whose mutations provoke an optic neuropathy. Since its first identification in 2000 the characterization of the functions of OPA1 has made rapid progress thus providing numerous clues to unravel the pathogenetic mechanisms of ADOA-1.
线粒体的形态根据细胞类型和细胞环境的不同而变化,从相互连接的丝状网络到孤立的点。这种形态可塑性取决于线粒体动力学,即分裂和融合两种拮抗力量之间的平衡。DRP1 和 FIS1 控制线粒体外膜的分裂,而 Mitofusins 则控制其融合。这篇综述重点介绍了 OPA1,它是为数不多的已知的内膜动力学因子之一,其突变会引发视神经病变。自 2000 年首次被鉴定以来,OPA1 的功能特征取得了快速进展,从而为阐明 ADOA-1 的发病机制提供了大量线索。