Institute for Research in Biomedicine (IRB Barcelona), Barcelona, Spain.
Semin Cell Dev Biol. 2010 Aug;21(6):566-74. doi: 10.1016/j.semcdb.2010.01.002. Epub 2010 Jan 15.
Mitochondria in mammalian cells are visualized as a network or as filaments that undergo continuous changes in shape and in localization within the cells. These changes are a consequence of the activity of different processes such as mitochondrial fusion and fission, and mitochondrial remodelling. In all, these processes are referred to as mitochondrial dynamics, and relevant questions, still unexplained, are why cells require such an active dynamics, or why mitochondria move to specific cellular regions. In this review we will summarize some of the biological functions assigned to the proteins identified as participating in mitochondrial fusion, namely mitofusin 1, mitofusin 2 and OPA1. In addition to the capacity of these proteins to promote fusion, mitofusin 2 or OPA1 regulate mitochondrial metabolism and loss-of-function reduces oxygen consumption and the capacity to oxidize substrates. We propose that mitochondrial fusion proteins operate as integrators of signals so they regulate both mitochondrial fusion and metabolism.
哺乳动物细胞中的线粒体呈现为网络状或丝状,其形状和在细胞内的定位不断发生变化。这些变化是线粒体融合和裂变以及线粒体重塑等不同过程活性的结果。总之,这些过程被称为线粒体动力学,而仍未得到解释的相关问题是,细胞为什么需要如此活跃的动力学,或者为什么线粒体移动到特定的细胞区域。在这篇综述中,我们将总结一些被认为参与线粒体融合的蛋白质的生物学功能,即线粒体融合蛋白 1、线粒体融合蛋白 2 和 OPA1。除了这些蛋白质促进融合的能力外,线粒体融合蛋白 2 或 OPA1 还调节线粒体代谢,功能丧失会降低耗氧量和氧化底物的能力。我们提出,线粒体融合蛋白作为信号整合因子发挥作用,因此它们既能调节线粒体融合,又能调节代谢。