WDR81抑制ikk介导的促生存基因表达,调控细胞凋亡。

IF 4.7 1区 生物学 Q1 MICROBIOLOGY
mBio Pub Date : 2025-10-03 DOI:10.1128/mbio.02722-25
Sannoong Hu, Pranav Danthi
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引用次数: 0

摘要

细胞凋亡是宿主对病毒感染的一种常见反应。感染后细胞凋亡的程度和时间是由细胞中激活诱导死亡和促进生存途径的信号强度之间的平衡控制的。在许多细胞类型中,哺乳动物呼肠孤病毒(呼肠孤病毒)感染导致细胞在感染后期通过凋亡诱导死亡。在本研究中,我们发现呼肠孤病毒感染后,WDR81 (WD repeat-containing protein 81, WDR81)是诱导细胞凋亡所必需的。诱导细胞凋亡需要WDR81并不是呼肠孤病毒所独有的,因为缺乏WDR81的细胞也能抵抗其他激动剂诱导的细胞凋亡。我们发现,在缺乏WDR81的细胞中,一些促生存基因的表达上调。这些基因的表达受κB激酶(IKK)复合物抑制剂- kB (NFκB)信号通路核因子的调控。当IKK信号在wdr81缺陷细胞中被阻断时,促生存基因的表达恢复到正常水平,细胞重新获得对细胞死亡触发器的易感性。我们的工作揭示了WDR81在控制细胞凋亡中的新功能。此外,它还揭示了内体细胞定位蛋白WDR81与IKK-NFκB信号传导之间先前未知的联系。病毒感染通常会导致被感染细胞的死亡。在病毒子代产生之前细胞死亡限制了感染向邻近细胞的传播,因此可能对宿主有益。然而,细胞死亡也可能导致组织破坏,并可能导致病毒性疾病。因此,了解细胞死亡是如何控制的是很重要的。在这里,我们发现了WD重复序列蛋白81 (WDR81)的细胞死亡调节作用,这是一种以前未涉及影响细胞死亡的细胞蛋白。我们发现,当这种蛋白质缺失时,细胞表达的生存信号水平要高得多。这些生存信号阻止有效诱导细胞死亡。通过研究这些存活信号的表达方式,我们揭示了WDR81与kB核因子(NFκB)之间的新联系,这是一种众所周知的细胞存活途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
WDR81 represses IKK-mediated expression of pro-survival genes to regulate apoptosis.

Apoptosis is a common host response to virus infection. The extent and timing of apoptosis following infection is controlled by the balance between the strength of signals that activate death-inducing and survival-promoting pathways in cells. In many cell types, infection with mammalian orthoreovirus (reovirus) results in induction of cell death by apoptosis late in infection. In this study, we uncovered that WD repeat-containing protein 81 (WDR81) is required for apoptosis induction after reovirus infection. The requirement for WDR81 for apoptosis induction is not unique to reovirus because cells lacking WDR81 are also resistant to apoptosis induced by other agonists. We find that in cells deficient in WDR81, expression of several pro-survival genes is upregulated. The expression of these genes is controlled by the inhibitor of κB kinase (IKK) complex-nuclear factor of kB (NFκB) signaling pathway. When IKK signaling is blocked in WDR81-deficient cells, pro-survival gene expression is restored to normal levels, and the cells regain their susceptibility to cell death triggers. Our work uncovers a new function for WDR81 in controlling apoptosis. Additionally, it reveals a previously unknown link between an endosomally localized protein, WDR81, and IKK-NFκB signaling.IMPORTANCEVirus infection often results in the death of the infected cells. Cell death prior to generation of virus progeny limits the spread of infection to neighboring cells and therefore can be beneficial to the host. However, cell death might also cause tissue destruction and could contribute to viral disease. It is therefore important to understand how cell death is controlled. Here, we uncover a cell death-regulating role for WD repeat-containing protein 81 (WDR81)-a cellular protein that has not been previously implicated in affecting cell death. We find that when this protein is absent, cells express a much greater level of survival signals. These survival signals prevent efficient induction of cell death. By investigating how these survival signals are expressed, we reveal a new link between WDR81 and nuclear factor of kB (NFκB), a well-known cellular survival pathway.

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来源期刊
mBio
mBio MICROBIOLOGY-
CiteScore
10.50
自引率
3.10%
发文量
762
审稿时长
1 months
期刊介绍: mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.
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