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p53表达在永生化颗粒细胞中环磷酸腺苷(cAMP)介导的细胞凋亡中的作用。

Involvement of p53 expression in cAMP-mediated apoptosis in immortalized granulosa cells.

作者信息

Keren-Tal I, Suh B S, Dantes A, Lindner S, Oren M, Amsterdam A

机构信息

Department of Hormone Research, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Exp Cell Res. 1995 May;218(1):283-95. doi: 10.1006/excr.1995.1157.

Abstract

In the accompanying paper we described the induction of apoptosis by extended cyclic AMP (cAMP)-mediated signals in primary granulosa cells and the reduction in this process in transformed cells expressing SV40 T antigen. In the present work, we examined the effect of overexpression of either wild-type or mutant p53 on cAMP-mediated apoptosis in steroidogenic granulosa cell lines transfected with SV40 DNA together with the Ha-ras oncogene and a temperature-sensitive variant of p53, p53val135. In cell lines expressing low amounts of T antigen and high amounts of p53val135, growth arrest was induced by transferring the cells from 37.5 degrees to 32 degrees C, a temperature which allows the manifestation of the wild-type phenotype of p53 and the induction of the WAF1 gene. While nonstimulated cells showed only a very modest apoptotic process, rapid and massive apoptosis was evident in cells stimulated by forskolin at 32 degrees C. The presence of serum could delay, but not abolish, this phenomenon. Progesterone production in such cells treated with cAMP was significantly higher at 32 degrees C than at 37.5 degrees C, suggesting that wild-type p53 can also enhance granulosa cell differentiation. Furthermore, at least at early stages, apoptosis is correlated with increased cell differentiation. On the other hand, in lines expressing high amounts of T antigen and low amounts of p53, neither an increase in cAMP-induced differentiation nor massive apoptosis was seen at 32 degrees C. These findings demonstrate that wild-type p53 can cooperate with cAMP-generated signals in the induction of steroidogenesis and of programmed cell death in granulosa cells.

摘要

在随附论文中,我们描述了延长的环磷酸腺苷(cAMP)介导的信号在原代颗粒细胞中诱导凋亡的情况,以及在表达SV40 T抗原的转化细胞中该过程的减少。在本研究中,我们检测了野生型或突变型p53过表达对用SV40 DNA、Ha-ras癌基因和p53的温度敏感变体p53val135转染的类固醇生成颗粒细胞系中cAMP介导的凋亡的影响。在表达少量T抗原和大量p53val135的细胞系中,将细胞从37.5℃转移至32℃可诱导生长停滞,此温度可使p53的野生型表型显现并诱导WAF1基因。未受刺激的细胞仅显示出非常适度的凋亡过程,而在32℃用福司可林刺激的细胞中,快速且大量的凋亡很明显。血清的存在可延迟但不能消除这种现象。在32℃用cAMP处理的此类细胞中孕酮的产生明显高于37.5℃,这表明野生型p53也可增强颗粒细胞分化。此外,至少在早期阶段,凋亡与细胞分化增加相关。另一方面,在表达大量T抗原和少量p53的细胞系中,在32℃既未观察到cAMP诱导的分化增加,也未观察到大量凋亡。这些发现表明野生型p53可与cAMP产生的信号协同作用,诱导颗粒细胞中的类固醇生成和程序性细胞死亡。

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