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4-羟基壬烯醛在应激诱导的程序性细胞死亡信号传导中的自我调节作用。

Self-regulatory role of 4-hydroxynonenal in signaling for stress-induced programmed cell death.

作者信息

Awasthi Yogesh C, Sharma Rajendra, Sharma Abha, Yadav Sushma, Singhal Sharad S, Chaudhary Pankaj, Awasthi Sanjay

机构信息

Department of Molecular Biology and Immunology, University of North Texas Health Science Center, Fort Worth, TX 76107-2699, USA.

出版信息

Free Radic Biol Med. 2008 Jul 15;45(2):111-8. doi: 10.1016/j.freeradbiomed.2008.04.007. Epub 2008 May 2.

Abstract

Within the last two decades, 4-hydroxynonenal has emerged as an important second messenger involved in the regulation of various cellular processes. Our recent studies suggest that HNE can induce apoptosis in various cells through the death receptor Fas (CD95)-mediated extrinsic pathway as well as through the p53-dependent intrinsic pathway. Interestingly, through its interaction with the nuclear protein Daxx, HNE can self-limit its apoptotic role by translocating Daxx to cytoplasm where it binds to Fas and inhibits Fas-mediated apoptosis. In this paper, after briefly describing recent studies on various biological activities of HNE, based on its interactions with Fas, Daxx, and p53, we speculate on possible mechanisms through which HNE may affect a multitude of cellular processes and draw a parallel between signaling roles of H(2)O(2) and HNE.

摘要

在过去二十年中,4-羟基壬烯醛已成为参与调节各种细胞过程的重要第二信使。我们最近的研究表明,HNE可通过死亡受体Fas(CD95)介导的外源性途径以及p53依赖性内源性途径诱导各种细胞凋亡。有趣的是,通过与核蛋白Daxx相互作用,HNE可将Daxx转运至细胞质,使其与Fas结合并抑制Fas介导的凋亡,从而自我限制其凋亡作用。在本文中,在简要描述了关于HNE各种生物学活性的近期研究后,基于其与Fas、Daxx和p53的相互作用,我们推测了HNE可能影响多种细胞过程的潜在机制,并对H₂O₂和HNE的信号传导作用进行了比较。

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