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聚合酶 I 和转录释放因子(PTRF)/钙卫蛋白-1 是一种新的应激诱导过早衰老的调节因子。

Polymerase I and transcript release factor (PTRF)/cavin-1 is a novel regulator of stress-induced premature senescence.

机构信息

Department of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261.

Department of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261.

出版信息

J Biol Chem. 2011 Aug 19;286(33):28657-28661. doi: 10.1074/jbc.C111.235119. Epub 2011 Jun 24.

Abstract

According to the "free radical theory" of aging, premature senescence induced by oxidative stress contributes to organismal aging. Polymerase I and transcript release factor (PTRF)/cavin-1 is a structural protein component of caveolae, invaginations of the plasma membrane involved in signal transduction. We show that oxidative stress up-regulates PTRF/cavin-1 protein expression and promotes the interaction between PTRF/cavin-1 and caveolin-1, another structural protein component of caveolae. Consistent with these data, the number of caveolae is dramatically increased in cells subjected to oxidative stress. We demonstrate that down-regulation of PTRF/cavin-1 by shRNA significantly inhibits oxidative stress-induced premature senescence. Mechanistically, we found that PTRF/cavin-1 expression is necessary for the oxidant-induced sequestration of Mdm2, a negative regulator of p53, into caveolar membranes, away from p53, and activation of the p53/p21(Waf1/Cip1) pathway. Expression of a mutant form of PTRF/cavin-1, which fails to localize to caveolar membranes after oxidative stress, inhibits oxidative stress-induced activation of p53 and induction of premature senescence. Thus, PTRF/cavin-1 is a novel regulator of oxidative stress-induced premature senescence by acting as a link between free radicals and activation of the p53/p21(Waf1/Cip1) pathway.

摘要

根据衰老的“自由基理论”,氧化应激诱导的过早衰老导致了机体衰老。聚合酶 I 和转录释放因子(PTRF)/ cavevin-1 是质膜凹陷小窝(参与信号转导)的结构蛋白成分。我们发现氧化应激上调 PTRF/cavin-1 蛋白表达,并促进 PTRF/cavin-1 与质膜另一种结构蛋白成分 caveolin-1 的相互作用。与这些数据一致,在受到氧化应激的细胞中,小窝的数量显著增加。我们证明通过 shRNA 下调 PTRF/cavin-1 可显著抑制氧化应激诱导的过早衰老。从机制上讲,我们发现 PTRF/cavin-1 表达对于氧化剂诱导的 Mdm2(p53 的负调节剂)隔离到质膜小窝中,远离 p53 并激活 p53/p21(Waf1/Cip1)途径是必需的。表达一种突变形式的 PTRF/cavin-1,其在氧化应激后不能定位到质膜小窝中,可抑制氧化应激诱导的 p53 激活和过早衰老的诱导。因此,PTRF/cavin-1 通过充当自由基和激活 p53/p21(Waf1/Cip1)途径之间的联系,成为氧化应激诱导的过早衰老的新型调节剂。

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