Autophagy as a Cellular Stress Response Mechanism in the Nervous System

被引:61
作者
Peker, Nesibe [1 ,2 ]
Gozuacik, Devrim [1 ,3 ,4 ]
机构
[1] Sabanci Univ, Fac Engn & Nat Sci, Mol Biol Genet & Bioengn Program, Tuzla, Turkey
[2] Nanyang Technol Univ, Sch Biol Sci, 60 Nanyang Dr, Singapore, Singapore
[3] Sabanci Univ, Nanotechnol Res & Applicat Ctr SUNUM, Tuzla, Turkey
[4] Ctr Excellence Funct Surfaces & Interfaces Nano D, Tuzla, Turkey
关键词
autophagy; cellular stress; nervous system; neuron; neurodegenerative disease; BASE-EXCISION-REPAIR; ENDOPLASMIC-RETICULUM TURNOVER; TRANSCRIPTION FACTOR NRF2; FOCAL CEREBRAL-ISCHEMIA; NEURAL STEM-CELLS; DNA-DAMAGE; OXIDATIVE STRESS; MOUSE MODEL; ALPHA-SYNUCLEIN; MOLECULAR-MECHANISMS;
D O I
10.1016/j.jmb.2020.01.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cells of an organism face with various types of insults during their lifetime. Exposure to toxins, metabolic problems, ischaemia/reperfusion, physical trauma, genetic diseases, neurodegenerative diseases are among the conditions that trigger cellular stress responses. In this context, autophagy is one of the mechanisms that supports cell survival under stressful conditions. Autophagic vesicle engulfs the cargo and transports it to lysosome for degradation and turnover. As such, autophagy eliminates abnormal proteins, clears damaged organelles, limits oxidative stress and helps to improve metabolic balance. Nervous system cells and particularly postmitotic neurons are highly sensitive to a spectrum of insults, and autophagy emerges as one of the key stress response mechanism, ensuring health and survival of these vulnerable cell types. In this review, we will overview mechanisms through which cells cope with stress, and how these stress responses regulate autophagy, with a special focus on the nervous system. (C) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2560 / 2588
页数:29
相关论文
共 274 条
[1]   The celecoxib derivatives AR-12 and AR-14 induce autophagy and clear prion-infected cells from prions [J].
Abdulrahman, Basant A. ;
Abdelaziz, Dalia ;
Thapa, Simrika ;
Lu, Li ;
Jain, Shubha ;
Gilch, Sabine ;
Proniuk, Stefan ;
Zukiwski, Alexander ;
Schatzl, Hermann M. .
SCIENTIFIC REPORTS, 2017, 7
[2]   NIPSNAP1 and NIPSNAP2 Act as "Eat Me" Signals for Mitophagy [J].
Abudu, Yakubu Princely ;
Pankiv, Serhiy ;
Mathai, Benan John ;
Lystad, Aif Hakon ;
Bindesboll, Christian ;
Brenne, Hanne Britt ;
Ng, Matthew Yoke Wui ;
Thiede, Bernd ;
Yamamoto, Ai ;
Nthiga, Thaddaeus Mutugi ;
Lamark, Trond ;
Esguerra, Camila, V ;
Johansen, Terje ;
Simonsen, Anne .
DEVELOPMENTAL CELL, 2019, 49 (04) :509-+
[3]  
ADAMS SL, 1975, J BIOL CHEM, V250, P9083
[4]   Cerebral ischemia-hypoxia induces intravascular coagulation and autophagy [J].
Adhami, Faisal ;
Liao, Guanghong ;
Morozov, Yury M. ;
Schloemer, Aryn ;
Schmithorst, Vincent J. ;
Lorenz, John N. ;
Dunn, R. Scott ;
Vorhees, Charles V. ;
Wills-Karp, Marsha ;
Degen, Jay L. ;
Davis, Roger J. ;
Mizushima, Noboru ;
Rakic, Pasko ;
Dardzinski, Bernard J. ;
Holland, Scott K. ;
Sharp, Frank R. ;
Kuan, Chia-Yi .
AMERICAN JOURNAL OF PATHOLOGY, 2006, 169 (02) :566-583
[5]   Short-term fasting induces profound neuronal autophagy [J].
Alirezaei, Mehrdad ;
Kemball, Christopher C. ;
Flynn, Claudia T. ;
Wood, Malcolm R. ;
Whitton, J. Lindsay ;
Kiosses, William B. .
AUTOPHAGY, 2010, 6 (06) :702-710
[6]   Endoplasmic reticulum stress signalling - from basic mechanisms to clinical applications [J].
Almanza, Aitor ;
Carlesso, Antonio ;
Chintha, Chetan ;
Creedican, Stuart ;
Doultsinos, Dimitrios ;
Leuzzi, Brian ;
Luis, Andreia ;
McCarthy, Nicole ;
Montibeller, Luigi ;
More, Sanket ;
Papaioannou, Alexandra ;
Pueschel, Franziska ;
Sassano, Maria Livia ;
Skoko, Josip ;
Agostinis, Patrizia ;
de Belleroche, Jackie ;
Eriksson, Leif A. ;
Fulda, Simone ;
Gorman, Adrienne M. ;
Healy, Sandra ;
Kozlov, Andrey ;
Munoz-Pinedo, Cristina ;
Rehm, Markus ;
Chevet, Eric ;
Samali, Afshin .
FEBS JOURNAL, 2019, 286 (02) :241-278
[7]   Protein aggregates in Huntington's disease [J].
Arrasate, Montserrat ;
Finkbeiner, Steven .
EXPERIMENTAL NEUROLOGY, 2012, 238 (01) :1-11
[8]   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
[9]   Cytoplasmic IRE1α-mediated XBP1 mRNA splicing in the absence of nuclear processing and endoplasmic reticulum stress [J].
Back, Sung Hoon ;
Lee, Kyungho ;
Vink, Elizabeth ;
Kaufman, Randal J. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (27) :18691-18706
[10]   Insulin-like Growth Factor-I Prevents the Accumulation of Autophagic Vesicles and Cell Death in Purkinje Neurons by Increasing the Rate of Autophagosome-to-lysosome Fusion and Degradation [J].
Bains, Mona ;
Florez-McClure, Maria L. ;
Heidenreich, Kim A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (30) :20398-20407