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Kelch 重复蛋白 KLHDC10 通过抑制 PP5 调节氧化应激诱导的 ASK1 激活。

The Kelch repeat protein KLHDC10 regulates oxidative stress-induced ASK1 activation by suppressing PP5.

机构信息

Laboratory of Cell Signaling, Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.

出版信息

Mol Cell. 2012 Dec 14;48(5):692-704. doi: 10.1016/j.molcel.2012.09.018. Epub 2012 Oct 25.

Abstract

Reactive oxygen species (ROS)-induced activation of Apoptosis signal-regulating kinase 1 (ASK1) plays crucial roles in oxidative stress-mediated cell death through the activation of the JNK and p38 MAPK pathways. However, the regulatory mechanism of ASK1 in the oxidative stress response remains to be elucidated. Here, we identified the kelch repeat protein, Slim, as an activator of ASK1 through a Drosophila misexpression screen. We also performed a proteomics screen and revealed that Kelch domain containing 10 (KLHDC10), a mammalian ortholog of Slim, interacted with Protein phosphatase 5 (PP5), which has been shown to inactivate ASK1 in response to ROS. KLHDC10 bound to the phosphatase domain of PP5 and suppressed its phosphatase activity. Moreover, KLHDC10 was required for H(2)O(2)-induced sustained activation of ASK1 and cell death in Neuro2A cells. These findings suggest that Slim/KLHDC10 is an activator of ASK1, contributing to oxidative stress-induced cell death through the suppression of PP5.

摘要

活性氧(ROS)诱导凋亡信号调节激酶 1(ASK1)的激活在氧化应激介导的细胞死亡中通过 JNK 和 p38 MAPK 途径的激活起着至关重要的作用。然而,ASK1 在氧化应激反应中的调节机制仍有待阐明。在这里,我们通过果蝇过表达筛选鉴定了 Kelch 重复蛋白 Slim 是 ASK1 的激活剂。我们还进行了蛋白质组学筛选,揭示了哺乳动物直系同源物 Kelch 结构域包含 10 号(KLHDC10)与蛋白磷酸酶 5(PP5)相互作用,PP5 已被证明在响应 ROS 时使 ASK1 失活。KLHDC10 与 PP5 的磷酸酶结构域结合并抑制其磷酸酶活性。此外,KLHDC10 是 H2O2 诱导的 Neuro2A 细胞中 ASK1 持续激活和细胞死亡所必需的。这些发现表明 Slim/KLHDC10 是 ASK1 的激活剂,通过抑制 PP5 促进氧化应激诱导的细胞死亡。

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