Oxidative stress and autophagy

被引:414
作者
Kiffin, R [1 ]
Bandyopadhyay, U [1 ]
Cuervo, AM [1 ]
机构
[1] Albert Einstein Coll Med, Dept Anat & Struct Biol, Marion Bessin Liver Res Ctr, Bronx, NY 10461 USA
关键词
D O I
10.1089/ars.2006.8.152
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
Organisms respond to oxidative injury by orchestrating a stress response to prevent further damage. An increase in the intracellular levels of anfioxidant agents, and at the same time the removal of already damaged components, are both part of the oxidative stress response. Lysosomes have been classically considered one of the main targets of the reactive oxygen species. In fact, the destabilization of the lysosomal membrane during oxidizing conditions promotes the leakage of the enzymes contained in these organelles and contributes to cellular damage. However, recent evidence supports a protective role of the lysosomal system, which can eliminate altered intracellular components through autophagy, at least in the first stages of oxidative injury. Consequently, activation of the main intracellular proteolytic systems, the ubiquitin/proteasome, and also the lysosomallautophagic system occurs during the oxidative stress response. The opposing roles for the lysosomal system under oxidizing conditions are discussed in this review.
引用
收藏
页码:152 / 162
页数:11
相关论文
共 85 条
[1]   An intralysosomal hsp70 is required for a selective pathway of lysosomal protein degradation [J].
Agarraberes, FA ;
Terlecky, SR ;
Dice, JF .
JOURNAL OF CELL BIOLOGY, 1997, 137 (04) :825-834
[2]   UPTAKE MICROAUTOPHAGY AND DEGRADATION OF EXOGENOUS PROTEINS BY ISOLATED RAT-LIVER LYSOSOMES - EFFECTS OF PH, ATP, AND INHIBITORS OF PROTEOLYSIS [J].
AHLBERG, J ;
GLAUMANN, H .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 1985, 42 (01) :78-88
[3]   Autophagic programmed cell death in Drosophila [J].
Baehrecke, EH .
CELL DEATH AND DIFFERENTIATION, 2003, 10 (09) :940-945
[4]   Selective degradation of peroxisomes in yeasts [J].
Bellu, AR ;
Kiel, JAKW .
MICROSCOPY RESEARCH AND TECHNIQUE, 2003, 61 (02) :161-170
[5]   The anti-ageing effects of caloric restriction may involve stimulation of macroautophagy and lysosomal degradation, and can be intensified pharmacologically [J].
Bergamini, E ;
Cavallini, G ;
Donati, A ;
Gori, Z .
BIOMEDICINE & PHARMACOTHERAPY, 2003, 57 (5-6) :203-208
[6]   Inhibition of the ATP-driven proton pump in RPE lysosomes by the major lipofuscin fluorophore A2-E may contribute to the pathogenesis of age-related macular degeneration [J].
Bergmann, M ;
Schütt, F ;
Holz, FG ;
Kopitz, J .
FASEB JOURNAL, 2004, 18 (01) :562-+
[7]   Inhibition of macroautophagy triggers apoptosis [J].
Boya, P ;
González-Polo, RA ;
Casares, N ;
Perfettini, JL ;
Dessen, P ;
Larochette, N ;
Métivier, D ;
Meley, D ;
Souquere, S ;
Yoshimori, T ;
Pierron, G ;
Codogno, P ;
Kroemer, G .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (03) :1025-1040
[8]   The Vid vesicle to vacuole trafficking event requires components of the SNARE membrane fusion machinery [J].
Brown, CR ;
Liu, JJ ;
Hung, GC ;
Carter, D ;
Cui, DY ;
Chiang, HL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (28) :25688-25699
[9]  
BRUNK UT, 1989, ADV EXP MED BIOL, V266, P313
[10]   Lipofuscin: Mechanisms of age-related accumulation and influence on cell function [J].
Brunk, UT ;
Terman, A .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 33 (05) :611-619