Endoplasmic Reticulum-Mitochondria Contact Sites-Emerging Intracellular Signaling Hubs

被引:39
作者
Aoyama-Ishiwatari, Saeko [1 ]
Hirabayashi, Yusuke [2 ]
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Tokyo, Japan
[2] Univ Tokyo, Sch Engn, Dept Chem & Biotechnol, Tokyo, Japan
关键词
mitochondria; ER; organelle contact sites; mammalian protein; tether; DEPENDENT ANION CHANNEL; MITOFUSIN; 2; PHOSPHATIDYLSERINE TRANSPORT; CA2+ HOMEOSTASIS; LIPID EXCHANGE; SMP DOMAINS; ER CONTACTS; PROTEINS; ORGANELLE; REVEALS;
D O I
10.3389/fcell.2021.653828
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It has become apparent that our textbook illustration of singular isolated organelles is obsolete. In reality, organelles form complex cooperative networks involving various types of organelles. Light microscopic and ultrastructural studies have revealed that mitochondria-endoplasmic reticulum (ER) contact sites (MERCSs) are abundant in various tissues and cell types. Indeed, MERCSs have been proposed to play critical roles in various biochemical and signaling functions such as Ca2+ homeostasis, lipid transfer, and regulation of organelle dynamics. While numerous proteins involved in these MERCS-dependent functions have been reported, how they coordinate and cooperate with each other has not yet been elucidated. In this review, we summarize the functions of mammalian proteins that localize at MERCSs and regulate their formation. We also discuss potential roles of the MERCS proteins in regulating multiple organelle contacts.
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页数:10
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