Sodium butyrate induces NIH3T3 cells to senescence-like state and enhances promoter activity of p21(WAF/CIP1) in p53-independent manner

被引:94
作者
Xiao, HY [1 ]
Hasegawa, T [1 ]
Miyaishi, O [1 ]
Ohkusu, K [1 ]
Isobe, K [1 ]
机构
[1] NATL INST LONGEV SCI,DEPT BASIC GERONTOL,MORIOKA,IWATE,JAPAN
关键词
D O I
10.1006/bbrc.1997.7158
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
Sodium butyrate, a histone deacetylase inhibitor, has been shown to induce differentiation of many cancer cells and senescence-like state of human fibroblasts. Here we show that sodium butyrate also induces senescence-like state of NIH3T3 cells. The treated cells were blocked at G1 phase and featured morphologically like senescent cells with enlarged cytoplasm and multiple nuclei. The expression of p21(WAF/CIP1) (p21) increased after sodium butyrate treatment at transcriptional level. To analyze the induction of promoter activity, we isolated 4.6 kb of murine p21 promoter and inserted it upstream of a luciferase reporter gene. When this construct was transiently transfected into NIH3T3 cells, sodium butyrate enhanced the luciferase activity. p53 independency of sodium butyrate-inducible p21 promoter activity was confirmed by using the deletion mutants lacking p53 binding sites and p53 deficient cells in transfection experiments. (C) 1997 Academic Press.
引用
收藏
页码:457 / 460
页数:4
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