The mitogen-inducible gene-6 is involved in regulation of cellular senescence in normal diploid fibroblasts

被引:11
作者
Xie, Bushan [1 ,2 ]
Zhao, Lin [1 ]
Chen, Hao [1 ]
Jin, Bo [1 ]
Mao, Zebin [1 ]
Yao, Zhi [3 ]
机构
[1] Peking Univ, Dept Biochem & Mol Biol, Hlth Sci Ctr, Beijing 100191, Peoples R China
[2] Nanchang Univ, Dept Gastroenterol, Affiliated Hosp 1, Nanchang 330006, Peoples R China
[3] Tianjin Med Univ, Dept Immunol, Tianjin 300070, Peoples R China
关键词
Cellular senescence; FOXO3a; Human fibroblasts; Mig-6; EPIDERMAL-GROWTH-FACTOR; ONCOGENE-INDUCED SENESCENCE; PREMATURE SENESCENCE; NEGATIVE REGULATOR; PROTEIN; SIGNAL; CELLS; RALT; SUPPRESSION; EXPRESSION;
D O I
10.1111/boc.201200052
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background informationThe mitogen-inducible gene-6 (Mig-6) is a non-kinase scaffolding adaptor protein. It has been shown that Mig-6 may play important roles in regulating stress response, maintaining homeostasis and functioning as a tumour suppressor. In this study, we investigated the role of Mig-6 in cellular senescence. ResultsOur results showed that Mig-6 is up-regulated during the senescence process. Functional analysis indicated that cells over-expressing Mig-6 have reduced DNA synthesis and showed the signs of senescence. Knockdown of Mig-6 delayed the initiation of Ras-induced cellular senescence. These results suggest that the increase of Mig-6 expression contributes to establishment of cellular senescence. Furthermore, our results showed that Mig-6 induction of senescence is related to its inhibition of EGF receptor (EGFR)/Erb B signalling. Subsequent analysis of the mechanism responsible for the up-regulation of its expression showed that FOXO3A transcriptionally up-regulates Mig-6 expression via directly binding to the FOXO response element in Mig-6 5-flanking regulatory sequences. ConclusionsMig-6 induces premature senescence via functioning in regulation of cellular senescence in normal diploid fibroblasts.
引用
收藏
页码:488 / 499
页数:12
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