Suppr超能文献

DJ-1 通过与凋亡信号调节激酶 1 的物理相互作用来调节 p38 丝裂原活化蛋白激酶通路。

DJ-1 modulates the p38 mitogen-activated protein kinase pathway through physical interaction with apoptosis signal-regulating kinase 1.

机构信息

Hormone Research Center, School of Biological Sciences and Technology, Chonnam National University, Yongbong-dong, Buk-ku, Gwangju 500-757, Republic of Korea.

出版信息

J Cell Biochem. 2010 May;110(1):229-37. doi: 10.1002/jcb.22530.

Abstract

DJ-1 has been reported as a gene linked to early onset familial Parkinson's disease, and is functionally involved in transcriptional regulation and oxidative stress-induced cell death. To understand the role of DJ-1 in cellular stress, this study investigated DJ-1's effect on stress-activated protein kinase signaling and H(2)O(2)-induced activation of apoptosis signal-regulating kinase 1 (ASK1). According to the results, the overexpression of DJ-1 inhibited H(2)O(2)-induced activation of ASK1 as well as the activation of downstream kinases in the p38 mitogen-activated protein kinase (MAPK) signaling cascade. The results of both in vivo binding and kinase studies have revealed that ASK1 is the direct target of DJ-1, whereas it has shown no effect on either MKK3 or p38. DJ-1 blocked both the homo-oligomerization of ASK1 and inhibited ASK1 activity. Taken together, our data strongly suggest that DJ-1, by directly inhibiting ASK1, may act as a negative regulator in ASK1 signaling cascades.

摘要

DJ-1 已被报道与早发性家族性帕金森病有关,其功能涉及转录调控和氧化应激诱导的细胞死亡。为了了解 DJ-1 在细胞应激中的作用,本研究探讨了 DJ-1 对应激激活蛋白激酶信号转导和 H2O2 诱导的凋亡信号调节激酶 1(ASK1)激活的影响。结果表明,DJ-1 的过表达抑制了 H2O2 诱导的 ASK1 以及 p38 丝裂原激活蛋白激酶(MAPK)信号级联中下游激酶的激活。体内结合和激酶研究的结果表明,ASK1 是 DJ-1 的直接靶标,而对 MKK3 或 p38 没有影响。DJ-1 阻断了 ASK1 的同源寡聚化并抑制了 ASK1 的活性。综上所述,我们的数据强烈表明,DJ-1 通过直接抑制 ASK1,可能作为 ASK1 信号级联中的负调节剂发挥作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验