Cristae Membrane Dynamics - A Paradigm Change

被引:101
作者
Kondadi, Arun Kumar [1 ]
Anand, Ruchika [1 ]
Reichert, Andreas S. [1 ]
机构
[1] Heinrich Heine Univ Dusseldorf, Med Fac, Inst Biochem & Mol Biol 1, D-40225 Dusseldorf, Germany
关键词
MITOCHONDRIAL CONTACT SITE; MICOS COMPONENT MIC60; INNER MEMBRANE; ATP SYNTHASE; ORGANIZING SYSTEM; CYTOCHROME-C; LIVE CELLS; COMPLEX; ORGANIZATION; CARDIOLIPIN;
D O I
10.1016/j.tcb.2020.08.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondria are dynamic organelles that have essential metabolic and regulatory functions. Earlier studies using electron microscopy (EM) revealed an immense diversity in the architecture of cristae - infoldings of the mitochondrial inner membrane (IM) - in different cells, tissues, bioenergetic and metabolic conditions, and during apoptosis. However, cristae were considered to be largely static entities. Recently, advanced super-resolution techniques have revealed that cristae are independent bioenergetic units that are highly dynamic and remodel on a timescale of seconds. These advances, coupled with mechanistic and structural studies on key molecular players, such as the MICOS (mitochondrial contact site and cristae organizing system) complex and the dynamin-like GTPase OPAL, have changed our view on mitochondria in a fundamental way. We summarize these recent findings and discuss their functional implications.
引用
收藏
页码:923 / 936
页数:14
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