C-Fos/C-Jun expression and AP-1 activation in skin fibroblasts from centenarians

被引:25
作者
Grassilli, E
Bellesia, E
Salomoni, P
Croce, MA
Sikora, E
Radziszewska, E
Tesco, G
Vergelli, M
Latorraca, S
Barbieri, D
Fagiolo, U
Santacaterina, S
Amaducci, L
Tiozzo, R
Sorbi, S
Franceschi, C
机构
[1] INRCA ANCONA, DEPT GERONTOL RES, I-60121 ANCONA, ITALY
[2] UNIV FLORENCE, DEPT NEUROL & PSYCHIAT SCI, I-50134 FLORENCE, ITALY
[3] UNIV PADUA, INST INTERNAL MED, I-35128 PADUA, ITALY
[4] M NENCKI INST EXPT BIOL, DEPT CELLULAR BIOCHEM, PL-02093 WARSAW, POLAND
关键词
D O I
10.1006/bbrc.1996.1387
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
In vitro replicative senescence is characterized by an irreversible growth arrest due to the inability of the cell to induce some key regulators of cell cycle progression, such as c-fos and AP-1, in response to mitogenic stimuli. In vitro replicative senescence and in vivo aging have been assumed to be two related phenomena, likely controlled by overlapping or interacting genes. As a corollary, fibroblasts from centenarians, which have undergone a long process of senescence in vivo should have very limited proliferative capability. On the contrary, in a previous work we found that fibroblasts from centenarians exhibited the same capacity to respond to different mitogenic stimuli as fibroblasts from young donors. Here we provide evidences that the well preserved proliferative response is likely due to the fact that some pivotal regulators-c-fos, c-jun and AP-1-are still fully inducible, despite a long procss of in vivo senescence. Our data therefore suggest that in vivo and in vitro aging are separate phenomena whose possible relationships, if any, have to be ascertained very carefully. (C) 1996 Academic Press, Inc.
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页码:517 / 523
页数:7
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