The Mitochondria-Endoplasmic Reticulum Contacts and Their Critical Role in Aging and Age-Associated Diseases

被引:114
作者
Moltedo, Ornella [1 ]
Remondelli, Paolo [2 ]
Amodio, Giuseppina [2 ]
机构
[1] Univ Salerno, Dept Pharm, Fisciano, Italy
[2] Scuola Med Saiemitana Univ Salerno, Dept Med Surg & Dent, Baronissi, Italy
关键词
aging; age-associated diseases; oxidative stress; senescence; endoplasmic reticulum; mitochondria; UNFOLDED PROTEIN RESPONSE; OXIDATIVE STRESS; MITOFUSIN; LIFE-SPAN; PHOSPHOLIPID TRANSFER; ALZHEIMERS-DISEASE; VAPB INTERACTS; ER MEMBRANES; CELL; AUTOPHAGY;
D O I
10.3389/fcell.2019.00172
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The recent discovery of interconnections between the endoplasmic reticulum (ER) membrane and those of almost all the cell compartments is providing novel perspectives for the understanding of the molecular events underlying cellular mechanisms in both physiological and pathological conditions. In particular, growing evidence strongly supports the idea that the molecular interactions occurring between ER and mitochondrial membranes, referred as the mitochondria (MT)-ER contacts (MERCs), may play a crucial role in aging and in the development of age-associated diseases. As emerged in the last decade, MERCs behave as signaling hubs composed by structural components that act as critical players in different age-associated disorders, such as neurodegenerative diseases and motor disorders, cancer, metabolic syndrome, as well as cardiovascular diseases. Age-associated disorders often derive from mitochondrial or ER dysfunction as consequences of oxidative stress, mitochondrial DNA mutations, accumulation of misfolded proteins, and defective organelle turnover. In this review, we discuss the recent advances associating MERCs to aging in the context of ER-MT crosstalk regulating redox signaling, ER-to MT lipid transfer, mitochondrial dynamics, and autophagy.
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页数:13
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