The role of autophagy in cardiovascular pathology

被引:70
作者
Gatica, Damian [1 ]
Chiong, Mario [2 ,3 ]
Lavandero, Sergio [2 ,3 ,4 ,5 ]
Klionsky, Daniel J. [1 ]
机构
[1] Univ Michigan, Life Sci Inst, Dept Mol Cellular & Dev Biol, 210 Washtenaw Ave, Ann Arbor, MI 48109 USA
[2] Univ Chile, Fac Ciencias Quim & Farmaceut, Adv Ctr Chron Dis ACCDiS, Dept Biochem & Mol Biol, Olivos 1007, Santiago 8380492, Chile
[3] Univ Chile, Fac Med, Olivos 1007, Santiago 8380492, Chile
[4] Corp Ctr Estudios Cient Enfermedades Cron CECEC, 926 JF Gonzalez, Santiago 7860201, Chile
[5] Univ Texas Southwestern Med Ctr Dallas, Dept Internal Med, Div Cardiol, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
Autophagosome; Cardiomyocyte; Heart; Lysosome; Vascular; ACTIVATED PROTEIN-KINASE; ENDOTHELIAL-CELL AUTOPHAGY; GROWTH-FACTOR-BETA; HEART-FAILURE; ENDOPLASMIC-RETICULUM; BECLIN; REGULATE AUTOPHAGY; SHEAR-STRESS; ULK1-MEDIATED PHOSPHORYLATION; DIABETIC CARDIOMYOPATHY;
D O I
10.1093/cvr/cvab158
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Macroautophagy/autophagy is a conserved catabolic recycling pathway in which cytoplasmic components are sequestered, degraded, and recycled to survive various stress conditions. Autophagy dysregulation has been observed and linked with the development and progression of several pathologies, including cardiovascular diseases, the leading cause of death in the developed world. In this review, we aim to provide a broad understanding of the different molecular factors that govern autophagy regulation and how these mechanisms are involved in the development of specific cardiovascular pathologies, including ischemic and reperfusion injury, myocardial infarction, cardiac hypertrophy, cardiac remodelling, and heart failure.
引用
收藏
页码:934 / 950
页数:17
相关论文
共 273 条
[1]   ATG8 Family Proteins Act as Scaffolds for Assembly of the ULK Complex SEQUENCE REQUIREMENTS FOR LC3-INTERACTING REGION (LIR) MOTIFS [J].
Alemu, Endalkachew Ashenafi ;
Lamark, Trond ;
Torgersen, Knut Martin ;
Birgisdottir, Aasa Birna ;
Larsen, Kenneth Bowitz ;
Jain, Ashish ;
Olsvik, Hallvard ;
Overvatn, Aud ;
Kirkin, Vladimir ;
Johansen, Terje .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (47) :39275-39290
[2]   Discordant signaling and autophagy response to fasting in hearts of obese mice: Implications for ischemia tolerance [J].
Andres, Allen M. ;
Kooren, Joel A. ;
Parker, Sarah J. ;
Tucker, Kyle C. ;
Ravindran, Nandini ;
Ito, Bruce R. ;
Huang, Chengqun ;
Venkatraman, Vidya ;
Van Eyk, Jennifer E. ;
Gottlieb, Roberta A. ;
Mentzer, Robert M., Jr. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2016, 311 (01) :H219-H228
[3]   Sirt7 Contributes to Myocardial Tissue Repair by Maintaining Transforming Growth Factor-β Signaling Pathway [J].
Araki, Satoshi ;
Izumiya, Yasuhiro ;
Rokutanda, Taku ;
Ianni, Alessandro ;
Hanatani, Shinsuke ;
Kimura, Yuichi ;
Onoue, Yoshiro ;
Senokuchi, Takafumi ;
Yoshizawa, Tatsuya ;
Yasuda, Osamu ;
Koitabashi, Norimichi ;
Kurabayashi, Masahiko ;
Braun, Thomas ;
Bober, Eva ;
Yamagata, Kazuya ;
Ogawa, Hisao .
CIRCULATION, 2015, 132 (12) :1081-1093
[4]   Beta2-adrenergic receptor regulates cardiac fibroblast autophagy and collagen degradation [J].
Aranguiz-Urroz, Pablo ;
Canales, Jimena ;
Copaja, Miguel ;
Troncoso, Rodrigo ;
Vicencio, Jose Miguel ;
Carrillo, Constanza ;
Lara, Hernan ;
Lavandero, Sergio ;
Diaz-Araya, Guillermo .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2011, 1812 (01) :23-31
[5]   The tumor suppressor PTEN positively regulates macroautophagy by inhibiting the phosphatidylinositol 3-kinase/protein kinase B pathway [J].
Arico, S ;
Petiot, A ;
Bauvy, C ;
Dubbelhuis, PF ;
Meijer, AJ ;
Codogno, P ;
Ogier-Denis, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (38) :35243-35246
[6]   Autophagosome formation from membrane compartments enriched in phosphatidylinositol 3-phosphate and dynamically connected to the endoplasmic reticulum [J].
Axe, Elizabeth L. ;
Walker, Simon A. ;
Manifava, Maria ;
Chandra, Priya ;
Roderick, H. Llewelyn ;
Habermann, Anja ;
Griffiths, Gareth ;
Ktistakis, Nicholas T. .
JOURNAL OF CELL BIOLOGY, 2008, 182 (04) :685-701
[7]   The eIF2α/ATF4 pathway is essential for stress-induced autophagy gene expression [J].
B'chir, Wafa ;
Maurin, Anne-Catherine ;
Carraro, Valerie ;
Averous, Julien ;
Jousse, Celine ;
Muranishi, Yuki ;
Parry, Laurent ;
Stepien, Georges ;
Fafournoux, Pierre ;
Bruhat, Alain .
NUCLEIC ACIDS RESEARCH, 2013, 41 (16) :7683-7699
[8]   The serine/threonine kinase ULK1 is a target of multiple phosphorylation events [J].
Bach, Markus ;
Larance, Mark ;
James, David E. ;
Ramm, Georg .
BIOCHEMICAL JOURNAL, 2011, 440 :283-291
[9]   Hypoxia-Induced Autophagy Is Mediated through Hypoxia-Inducible Factor Induction of BNIP3 and BNIP3L via Their BH3 Domains [J].
Bellot, Gregory ;
Garcia-Medina, Raquel ;
Gounon, Pierre ;
Chiche, Johanna ;
Roux, Daniele ;
Pouyssegur, Jacques ;
Mazure, Nathalie M. .
MOLECULAR AND CELLULAR BIOLOGY, 2009, 29 (10) :2570-2581
[10]   Endothelial Cell Autophagy Maintains Shear Stress-Induced Nitric Oxide Generation via Glycolysis-Dependent Purinergic Signaling to Endothelial Nitric Oxide Synthase [J].
Bharath, Leena P. ;
Cho, Jae Min ;
Park, Seul-Ki ;
Ruan, Ting ;
Li, Youyou ;
Mueller, Robert ;
Bean, Tyler ;
Reese, Van ;
Richardson, Russel S. ;
Cai, Jinjin ;
Sargsyan, Ashot ;
Pires, Karla ;
Babu, Pon Velayutham Anandh ;
Boudina, Sihem ;
Graham, Timothy E. ;
Symons, J. David .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2017, 37 (09) :1646-+