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.