Proteolytic response to oxidative stress in mammalian cells

被引:51
作者
Mehlhase, J [1 ]
Grune, T [1 ]
机构
[1] Humboldt Univ, Fac Med Charite, Neurosci Res Ctr, D-10117 Berlin, Germany
关键词
calpains; lysosomes; proteasome; protein oxidation; proteolysis;
D O I
10.1515/BC.2002.057
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
Oxidative stress in mammalian cells is an inevitable consequence of their aerobic metabolism. The production of reactive oxygen and nitric oxide species causes oxidative modifications of proteins often combined with a loss of their biological function. Like most partially denatured proteins, moderately oxidized proteins are more sensitive to proteolytic attack by proteases. The diverse cellular proteolytic systems are an important secondary defense against oxidative stress by degrading oxidized and damaged proteins, thereby preventing their intracellular accumulation. In mammalian cells, a range of proteases exists which are distributed throughout the cell. In this review we summarize the function of the cytosolic (proteasome and calpains), the lysosomal, the mitochondrial and the nuclear proteolytic pathways in response to oxidative stress. Particular emphasis is given to the proteasomal system, since this pathway appears to be the most important proteolytic system involved in the removal of oxidatively modified or damaged proteins.
引用
收藏
页码:559 / 567
页数:9
相关论文
共 126 条
  • [1] Adamo AM, 1999, J NEUROSCI RES, V55, P523, DOI 10.1002/(SICI)1097-4547(19990215)55:4<523::AID-JNR12>3.0.CO
  • [2] 2-Q
  • [3] Calcium-dependent proteolysis in rabbit lens epithelium after oxidative stress
    Andersson, M
    Sjöstrand, J
    Petersen, A
    Karlsson, JO
    [J]. OPHTHALMIC RESEARCH, 1998, 30 (03) : 157 - 167
  • [4] The hydrophobic effect contributes to polyubiquitin chain recognition
    Beal, RE
    Toscano-Cantaffa, D
    Young, P
    Rechsteiner, M
    Pickart, CM
    [J]. BIOCHEMISTRY, 1998, 37 (09) : 2925 - 2934
  • [5] Protein oxidation in aging, disease, and oxidative stress
    Berlett, BS
    Stadtman, ER
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (33) : 20313 - 20316
  • [6] Bota Daniela A., 2000, Free Radical Biology and Medicine, V29, pS80
  • [7] Subcellular localization of proteasomes and their regulatory complexes in mammalian cells
    Brooks, P
    Fuertes, G
    Murray, RZ
    Bose, S
    Knecht, E
    Rechsteiner, MC
    Hendil, KB
    Tanaka, K
    Dyson, J
    Rivett, AJ
    [J]. BIOCHEMICAL JOURNAL, 2000, 346 : 155 - 161
  • [8] Responses to peroxynitrite in yeast: Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as a sensitive intracellular target for nitration and enhancement of chaperone expression and ubiquitination
    Buchczyk, DP
    Briviba, K
    Harti, FU
    Sies, H
    [J]. BIOLOGICAL CHEMISTRY, 2000, 381 (02) : 121 - 126
  • [9] From Cytoprotection to Tumor Suppression: The Multifactorial Role of Peroxiredoxins
    Butterfield, Lisa H.
    Merino, Alejandro
    Golub, Sidney H.
    Shau, Hungyi
    [J]. ANTIOXIDANTS & REDOX SIGNALING, 1999, 1 (04) : 385 - 402
  • [10] MODULATION OF THE HYDROPHOBICITY OF GLUTAMINE-SYNTHETASE BY MIXED-FUNCTION OXIDATION
    CERVERA, J
    LEVINE, RL
    [J]. FASEB JOURNAL, 1988, 2 (10) : 2591 - 2595