Mitochondrial Contact Sites in Inflammation-Induced Cardiovascular Disease

被引:16
作者
Liu, Hao [1 ,2 ]
Liu, Xiao [1 ,2 ]
Zhuang, Haixia [2 ]
Fan, Hualin [2 ,3 ]
Zhu, Dongxing [4 ]
Xu, Yiming [5 ]
He, Pengcheng [6 ]
Liu, Jinbao [1 ,2 ]
Feng, Du [1 ,2 ]
机构
[1] Guangzhou Med Univ, Affiliated Canc Hosp & Inst, Guangzhou, Peoples R China
[2] Guangzhou Med Univ, Sch Basic Med Sci, Guangzhou Municipal & Guangdong Prov Key Lab Prot, State Key Lab Resp Dis, Guangzhou, Peoples R China
[3] South China Univ Technol, Guangdong Prov Peoples Hosp, Sch Med, Guangzhou, Peoples R China
[4] Guangzhou Med Univ, Affiliated Hosp 2, Sch Basic Med Sci, Guangzhou Inst Cardiovasc Dis,Key Lab Cardiovasc, Guangzhou, Peoples R China
[5] Guangzhou Med Univ, Sch Basic Med Sci, Guangzhou, Peoples R China
[6] Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Guangdong Cardiovasc Inst, Dept Cardiol,Guangdong Prov Key Lab Coronary Hear, Guangzhou, Peoples R China
关键词
mitochondrial-associated membranes; mitochondria; autophagy; cardiovascular disease; inflammation; inflammasome; ENDOPLASMIC-RETICULUM MEMBRANES; HUMAN ATHEROSCLEROTIC PLAQUES; NOGO-B RECEPTOR; NLRP3; INFLAMMASOME; ACCELERATED ATHEROSCLEROSIS; DIABETIC CARDIOMYOPATHY; STRUCTURAL-CHANGES; HEART-FAILURE; FRACTIONS; CA2+ UPTAKE;
D O I
10.3389/fcell.2020.00692
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mitochondrion, the ATP-producing center, is both physically and functionally associated with almost all other organelles in the cell. Mitochondrial-associated membranes (MAMs) are involved in a variety of biological processes, such as lipid exchange, protein transport, mitochondrial fission, mitophagy, and inflammation. Several inflammation-related diseases in the cardiovascular system involve several intracellular events including mitochondrial dysfunction as well as disruption of MAMs. Therefore, an in-depth exploration of the function of MAMs will be of great significance for us to understand the initiation, progression, and clinical complications of cardiovascular disease (CVD). In this review, we summarize the recent advances in our knowledge of MAM regulation and function in CVD-related cells. We discuss the potential roles of MAMs in activating inflammation to influence the development of CVD.
引用
收藏
页数:15
相关论文
共 143 条
[51]   Linking endothelial dysfunction with endothelial cell activation [J].
Liao, James K. .
JOURNAL OF CLINICAL INVESTIGATION, 2013, 123 (02) :540-541
[52]   Progress and challenges in translating the biology of atherosclerosis [J].
Libby, Peter ;
Ridker, Paul M. ;
Hansson, Goran K. .
NATURE, 2011, 473 (7347) :317-325
[53]   Role of NLRP3 inflammasome in the pathogenesis of cardiovascular diseases [J].
Liu, Dongling ;
Zeng, Xiang ;
Li, Xiao ;
Mehta, Jawahar L. ;
Wang, Xianwei .
BASIC RESEARCH IN CARDIOLOGY, 2018, 113 (01)
[54]   Mitochondrial 'kiss-and-run': interplay between mitochondrial motility and fusion-fission dynamics [J].
Liu, Xingguo ;
Weaver, David ;
Shirihai, Orian ;
Hajnoczky, Gyoergy .
EMBO JOURNAL, 2009, 28 (20) :3074-3089
[55]   Sarcoplasmic reticulum-mitochondria communication in cardiovascular pathophysiology [J].
Lopez-Crisosto, Camila ;
Pennanen, Christian ;
Vasquez-Trincado, Cesar ;
Morales, PabloE. ;
Bravo-Sagua, Roberto ;
Quest, Andrew F. G. ;
Chiong, Mario ;
Lavandero, Sergio .
NATURE REVIEWS CARDIOLOGY, 2017, 14 (06) :342-360
[56]   Mitochondrial dysfunction and type 2 diabetes [J].
Lowell, BB ;
Shulmanz, GI .
SCIENCE, 2005, 307 (5708) :384-387
[57]   Innate immune recognition receptors and damage-associated molecular patterns in plaque inflammation [J].
Lundberg, Anna M. ;
Yan, Zhong-qun .
CURRENT OPINION IN LIPIDOLOGY, 2011, 22 (05) :343-349
[58]   Rosuvastatin Alleviates Diabetic Cardiomyopathy by Inhibiting NLRP3 Inflammasome and MAPK Pathways in a Type 2 Diabetes Rat Model [J].
Luo, Beibei ;
Li, Bo ;
Wang, Wenke ;
Liu, Xiangjuan ;
Liu, Xiaoman ;
Xia, Yanfei ;
Zhang, Cheng ;
Zhang, Yun ;
Zhang, Mingxiang ;
An, Fengshuang .
CARDIOVASCULAR DRUGS AND THERAPY, 2014, 28 (01) :33-43
[59]   CTLA4-IgG ameliorates homocysteine-accelerated atherosclerosis by inhibiting T-cell overactivation in apoE/ mice [J].
Ma, Kongyang ;
Lv, Silin ;
Liu, Bo ;
Liu, Ziyi ;
Luo, Yuhong ;
Kong, Wei ;
Xu, Qingbo ;
Feng, Juan ;
Wang, Xian .
CARDIOVASCULAR RESEARCH, 2013, 97 (02) :349-359
[60]   Targeting inflammation to reduce cardiovascular disease risk [J].
Maffia, Pasquale ;
Cirino, Giuseppe .
BRITISH JOURNAL OF PHARMACOLOGY, 2017, 174 (22) :3895-3897