Starvation-induced phosphorylation activates gasdermin A to initiate pyroptosis

IF 7.5 1区 生物学 Q1 CELL BIOLOGY Cell reports Pub Date : 2024-09-10 DOI:10.1016/j.celrep.2024.114728
Xinran Li, Xiao Li, Cong Xiang, Jin Cao, Jiansheng Guo, Shilei Zhu, Jingyi Tan, Lijing Wang, Chun Gao, Shengduo Liu, Lifeng Zhao, Bo Yuan, Pinglong Xu, Bing Yang, Dali Li, Bin Zhao, Xin-Hua Feng
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Abstract

Pyroptosis, a pro-inflammatory form of programmed cell death, is crucial for host defense against pathogens and danger signals. Proteolytic cleavage of gasdermin proteins B–E (GSDMB–GSDME) is well established as a trigger for pyroptosis, but the intracellular activation mechanism of GSDMA remains elusive. Here, we demonstrate that severe starvation induces pyroptosis through phosphorylation-induced activation of GSDMA. Nutrient stresses stimulate GSDMA activation via phosphorylation mediated by Unc-51-like autophagy-activating kinase 1 (ULK1). Phosphorylation of Ser353 on human GSDMA by ULK1 or the phospho-mimetic Ser353Asp mutant of GSDMA liberates GSDMA from auto-inhibition, facilitating its membrane targeting and initiation of pyroptosis. To further validate the significance of GSDMA phosphorylation, we generated a constitutively active mutant Ser354Asp of mouse Gsdma, which induced skin inflammation and hyperplasia in mice, reminiscent of phenotypes with activated Gsdma. This study uncovers phosphorylation of GSDMA as a mechanism underlying pyroptosis initiation and cellular response to nutrient stress.

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饥饿诱导的磷酸化激活了气蛋白 A,从而启动了热蛋白沉积症
化脓作用是一种程序性细胞死亡的促炎形式,对于宿主抵御病原体和危险信号至关重要。气敏蛋白 B-E (GSDMB-GSDME)的蛋白水解裂解已被证实是裂解热的触发因素,但 GSDMA 的细胞内激活机制仍未确定。在这里,我们证明了严重饥饿通过磷酸化诱导的 GSDMA 激活来诱导热凋亡。营养应激通过Unc-51样自噬激活激酶1(ULK1)介导的磷酸化刺激GSDMA活化。ULK1或GSDMA的磷酸化拟态Ser353Asp突变体将人GSDMA上的Ser353磷酸化,从而使GSDMA摆脱自身抑制,促进其膜靶向和启动热噬。为了进一步验证 GSDMA 磷酸化的重要性,我们生成了小鼠 Gsdma 的组成型活性突变体 Ser354Asp,它能诱导小鼠皮肤炎症和增生,与活化的 Gsdma 表型相似。这项研究揭示了GSDMA的磷酸化机制,它是热核病启动和细胞对营养应激反应的基础。
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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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