Identification of 30 protein species involved in replicative senescence and stress-induced premature senescence

被引:52
作者
Dierick, JF
Kalume, DE
Wenders, F
Salmon, M
Dieu, M
Raes, M
Roepstorff, P
Toussaint, O
机构
[1] Univ Namur, FUNDP, Dept Biol, Unit Res Cellular Biol,URBC, B-5000 Namur, Belgium
[2] Odense Univ, Univ So Denmark, Prot Res Grp, DK-5230 Odense M, Denmark
关键词
stress; replicative senescence; proteomics; mass spectrometry; molecular scars; in vitro toxicology;
D O I
10.1016/S0014-5793(02)03604-9
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
Exposure of human proliferative cells to subcytotoxic stress triggers stress-induced premature senescence (SIPS) which is characterized by many biomarkers of replicative senescence. Proteomic comparison of replicative senescence and stress-induced premature senescence indicates that, at the level of protein expression, stress-induced premature senescence and replicative senescence are different phenotypes sharing however similarities. In this study, we identified 30 proteins showing changes of expression level specific or common to replicative senescence and/or stress-induced premature senescence. These changes affect different cell functions, including energy metabolism, defense systems, maintenance of the redox potential, cell morphology and transduction pathways. (C) 2002 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:499 / 504
页数:6
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