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