Proteolysis of oxidised proteins and cellular senescence

被引:54
作者
Merker, K
Grune, T
机构
[1] Humboldt Univ, Fac Med Charite, Clin Phys Med, D-10098 Berlin, Germany
[2] Humboldt Univ, Fac Med Charite, Clin Rehabil, D-10098 Berlin, Germany
关键词
protein oxidation; proteolysis; proteasome; ageing; cellular senescence;
D O I
10.1016/S0531-5565(00)00140-6
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Aerobe living is consequently connected with a permanent oxidation of cellular proteins. Free radicals and other oxidants damage the normal intracellular protein pool. Therefore. the prevention of accumulation of oxidised cellular proteins is one of the major functions of the proteolytic machinery of mammalian cells. It is known that the multicatalytic proteinase complex, the proteasome, is the major protease that is able to recognise and degrade oxidised proteins. Cellular models are most useful to investigate biochemical changes of protein catabolism during senescence. Unfortunately, little is known about the protein turnover and the regulation of the proteasomal system as well as under oxidative stress conditions as during senescence. The proteasomal regulation during oxidative stress, protein oxidation and the changes of these processes during the ageing process are highlighted in this review. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:779 / 786
页数:8
相关论文
共 29 条
[1]   Differential oxidative damage to mitochondrial proteins during aging [J].
Agarwal, S ;
Sohal, RS .
MECHANISMS OF AGEING AND DEVELOPMENT, 1995, 85 (01) :55-63
[2]   AGING AND PROTEIN OXIDATIVE DAMAGE [J].
AGARWAL, S ;
SOHAL, RS .
MECHANISMS OF AGEING AND DEVELOPMENT, 1994, 75 (01) :11-19
[3]   AGING AND PROTEOLYSIS OF OXIDIZED PROTEINS [J].
AGARWAL, S ;
SOHAL, RS .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1994, 309 (01) :24-28
[4]  
AGARWAL S, 1996, EXP GERONTOL, V31, P3387
[5]  
BRADLEY MO, 1976, J BIOL CHEM, V251, P3521
[6]  
BRUNK UT, 1998, UNDERSTANDING PROCES, P229
[7]   PROTEIN OXIDATION AND AGING .1. DIFFICULTIES IN MEASURING REACTIVE PROTEIN CARBONYLS IN TISSUES USING 2,4-DINITROPHENYLHYDRAZINE [J].
CAO, GH ;
CUTLER, RG .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1995, 320 (01) :106-114
[8]   REVERSAL OF AGE-RELATED INCREASE IN BRAIN PROTEIN OXIDATION, DECREASE IN ENZYME-ACTIVITY, AND LOSS IN TEMPORAL AND SPATIAL MEMORY BY CHRONIC ADMINISTRATION OF THE SPIN-TRAPPING COMPOUND N-TERT-BUTYL-ALPHA-PHENYLNITRONE [J].
CARNEY, JM ;
STARKEREED, PE ;
OLIVER, CN ;
LANDUM, RW ;
CHENG, MS ;
WU, JF ;
FLOYD, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) :3633-3636
[9]   Proteasome inactivation upon aging and on oxidation-effect of HSP 90 [J].
Conconi, M ;
Friguet, B .
MOLECULAR BIOLOGY REPORTS, 1997, 24 (1-2) :45-50
[10]   Age-related decline of rat liver multicatalytic proteinase activity and protection from oxidative inactivation by heat-shock protein 90 [J].
Conconi, M ;
Szweda, LI ;
Levine, RL ;
Stadtman, ER ;
Friguet, B .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1996, 331 (02) :232-240