Hippo通路激酶MST1介导一个反馈回路来维持NLRP3炎性小体的稳态。

IF 6.9 1区 生物学 Q1 CELL BIOLOGY
Xiawei Huang, Jiahui Wang, Yao Liu, Huimin Pan, Kewei Zheng, Bo Liu
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引用次数: 0

摘要

炎性小体在炎症反应中起关键作用。然而,它们的活性必须严格控制,以防止过度激活和随后的炎症性疾病。负反馈回路代表了维持信号稳态的一般机制,然而炎性小体利用这一过程防止过度激活的机制尚不清楚。在这里,我们发现了一个由Hippo通路激酶哺乳动物ste20样激酶1 (MST1)介导的负反馈回路,该回路可防止NLRP3炎性体的过度激活。在机制上,NLRP3炎性小体激活诱导caspase-1依赖性MST1在其抑制连接区域的裂解,导致激酶活性增强。增强的MST1磷酸化炎性小体适配蛋白ASC的丝氨酸58,破坏ASC的寡聚化,从而减弱炎性小体的组装。值得注意的是,staurosporine (STS)是一种MST1裂解的化学诱导剂,可以减轻脂多糖(LPS)诱导的脓毒症小鼠模型中的炎症和组织损伤。这些发现揭示了维持炎症稳态的负反馈机制,并突出了MST1切割作为控制炎症的潜在治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Hippo pathway kinase MST1 mediates a feedback loop to maintain NLRP3 inflammasome homeostasis.

Inflammasomes play pivotal roles in inflammatory responses. However, their activity must be tightly controlled to prevent overactivation and subsequent inflammatory diseases. Negative feedback loops represent a general mechanism to maintain signaling homeostasis, yet the mechanisms by which inflammasomes employ this process to prevent overactivation remain poorly understood. Here, we identify a negative feedback loop mediated by the Hippo pathway kinase mammalian Ste20-like kinase 1 (MST1) that prevents hyperactivation of the NLRP3 inflammasome. Mechanistically, NLRP3 inflammasome activation induces caspase-1-dependent cleavage of MST1 on its inhibitory linker region, resulting in enhanced kinase activity. The enhanced MST1 phosphorylates the inflammasome adaptor protein ASC at serine 58, disrupting ASC oligomerization and thereby attenuating inflammasome assembly. Notably, staurosporine (STS), a chemical inducer of MST1 cleavage, mitigates inflammation and tissue damage in a lipopolysaccharide (LPS)-induced sepsis mouse model. These findings reveal a negative feedback mechanism for maintaining inflammatory homeostasis and highlight MST1 cleavage as a potential therapeutic target for controlling inflammation.

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来源期刊
Cell reports
Cell reports CELL BIOLOGY-
CiteScore
13.80
自引率
1.10%
发文量
1305
审稿时长
77 days
期刊介绍: Cell Reports publishes high-quality research across the life sciences and focuses on new biological insight as its primary criterion for publication. The journal offers three primary article types: Reports, which are shorter single-point articles, research articles, which are longer and provide deeper mechanistic insights, and resources, which highlight significant technical advances or major informational datasets that contribute to biological advances. Reviews covering recent literature in emerging and active fields are also accepted. The Cell Reports Portfolio includes gold open-access journals that cover life, medical, and physical sciences, and its mission is to make cutting-edge research and methodologies available to a wide readership. The journal's professional in-house editors work closely with authors, reviewers, and the scientific advisory board, which consists of current and future leaders in their respective fields. The advisory board guides the scope, content, and quality of the journal, but editorial decisions are independently made by the in-house scientific editors of Cell Reports.
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