ER-mitochondria contact sites; a multifaceted factory for Ca2+ signaling and lipid transport

被引:28
|
作者
Sassano, Maria Livia [1 ,2 ]
Felipe-Abrio, Blanca [1 ,2 ]
Agostinis, Patrizia [1 ,2 ]
机构
[1] Cell Death Res & Therapy Grp, Dept Cellular & Mol Med, Leuven, Belgium
[2] Ctr Canc Biol VIB, Leuven, Belgium
关键词
ER-mitochondria contact sites; lipids; lipid transfer protein; Ca2+ signaling; cancer; ENDOPLASMIC-RETICULUM; MEMBRANE-FRACTION; MITOFUSIN; REGULATES APOPTOSIS; BH4; DOMAIN; COMPLEX-I; CARDIOLIPIN; PHOSPHATIDYLSERINE; PHOSPHATIDYLETHANOLAMINE; DYNAMICS;
D O I
10.3389/fcell.2022.988014
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Membrane contact sites (MCS) between organelles of eukaryotic cells provide structural integrity and promote organelle homeostasis by facilitating intracellular signaling, exchange of ions, metabolites and lipids and membrane dynamics. Cataloguing MCS revolutionized our understanding of the structural organization of a eukaryotic cell, but the functional role of MSCs and their role in complex diseases, such as cancer, are only gradually emerging. In particular, the endoplasmic reticulum (ER)-mitochondria contacts (EMCS) are key effectors of non-vesicular lipid trafficking, thereby regulating the lipid composition of cellular membranes and organelles, their physiological functions and lipid-mediated signaling pathways both in physiological and diseased conditions. In this short review, we discuss key aspects of the functional complexity of EMCS in mammalian cells, with particular emphasis on their role as central hubs for lipid transport between these organelles and how perturbations of these pathways may favor key traits of cancer cells.
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页数:13
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