The role of Gαq in regulating NLRP3 inflammasome activation.

IF 4.8 3区 医学 Q2 CELL BIOLOGY Inflammation Research Pub Date : 2024-10-26 DOI:10.1007/s00011-024-01961-x
Ruixue Kong, Lijun Peng, Honggang Bao, Lulu Sun, Yan Feng, Hua Li, Dashan Wang
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Abstract

Background: G proteins are a class of important signal transducers in mammalians. G proteins can corpoarated with G proteincoupled receptors (GPCRs) and transmit signals from extracellular stimuli into intracellular response, which will regulate a series of biological functions. G-proteins are heterotrimeric proteins composed of Gα, Gβ, and Gγ subunits. Based on structural and functional similarity of their α-subunits, G proteins are typically grouped into four classes (Gi, Gs, Gq/11, and G12/13). The Gq/11 subfamily consists of Gq, G11, G14, and G15/16 proteins. Gαq is the α-subunit of Gq protein and encoded by GNAQ. Our previous studies revealed that Gαq play an important role in regulating T cell survival and T cell differentiation. Inflammasomes are multiprotein complexes that play a critical role in modulating innate inflammatory response. NLRP3 inflammasome is currently the most extensively studied inflammasome.

Methods: We found that Gαq suppressed NLRP3 inflammasome activation in macrophage, Gαq also suppressed NLRP3 inflammasome activation in a LPS-induced sepsis mouse model. Gαq can locate to mitochondria and Gαq was required for the maintenance of mitochondrial homeostasis. Gαq regulated NLRP3 inflammasome activation by modulating mitochondrial reactive oxygen species (mtROS).

Results: We found that Gαq suppressed NLRP3 inflammasome activation in macrophage, Gαq also suppressed NLRP3 inflammasome activation in a LPS-induced sepsis mouse model. Gαq can locate to mitochondria and Gαq was required for the maintenance of mitochondrial homeostasis. Gαq regulated NLRP3 inflammasome activation by modulating mitochondrial reactive oxygen species (mtROS).

Conclusion: Our results indicate that Gαq regulates NLRP3 inflammasome activation by modulating mitochondrial ROS production. Our research provides new mechanistic insight into the activation of NLRP3 inflammasome. As it has been proved that NLRP3 inflammasome plays an important role in the pathogenesis many diseases such as Alzheimer's disease, cancer, and inflammatory bowel disease, Gαq might become a novel drug target for these diseases in future.

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Gαq 在调节 NLRP3 炎症小体活化中的作用。
背景:G 蛋白是哺乳动物体内一类重要的信号转换器。G蛋白可与G蛋白偶联受体(GPCR)结合,将细胞外刺激信号转导为细胞内反应,从而调控一系列生物功能。G 蛋白是由 Gα、Gβ 和 Gγ 亚基组成的异源三聚体蛋白。根据其 α 亚基的结构和功能相似性,G 蛋白通常被分为四类(Gi、Gs、Gq/11 和 G12/13)。Gq/11 亚家族由 Gq、G11、G14 和 G15/16 蛋白组成。Gαq 是 Gq 蛋白的 α-亚基,由 GNAQ 编码。我们之前的研究发现,Gαq 在调节 T 细胞存活和 T 细胞分化方面发挥着重要作用。炎症小体是一种多蛋白复合物,在调节先天性炎症反应中发挥着关键作用。NLRP3炎性体是目前研究最为广泛的炎性体:我们发现,Gαq能抑制巨噬细胞中NLRP3炎性体的活化,在LPS诱导的败血症小鼠模型中,Gαq也能抑制NLRP3炎性体的活化。Gαq 可以定位到线粒体,线粒体平衡的维持需要 Gαq 的参与。Gαq通过调节线粒体活性氧(mtROS)来调控NLRP3炎性体的激活:结果:我们发现Gαq抑制了巨噬细胞中NLRP3炎性体的活化,Gαq还抑制了LPS诱导的败血症小鼠模型中NLRP3炎性体的活化。Gαq可以定位到线粒体,线粒体平衡的维持需要Gαq。Gαq通过调节线粒体活性氧(mtROS)来调控NLRP3炎性体的激活:我们的研究结果表明,Gαq通过调节线粒体ROS的产生来调控NLRP3炎性体的激活。我们的研究为 NLRP3 炎症小体的活化提供了新的机制认识。由于 NLRP3 炎症小体已被证实在阿尔茨海默病、癌症和炎症性肠病等多种疾病的发病机制中扮演重要角色,Gαq 未来可能成为治疗这些疾病的新药靶点。
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来源期刊
Inflammation Research
Inflammation Research 医学-免疫学
CiteScore
9.90
自引率
1.50%
发文量
134
审稿时长
3-8 weeks
期刊介绍: Inflammation Research (IR) publishes peer-reviewed papers on all aspects of inflammation and related fields including histopathology, immunological mechanisms, gene expression, mediators, experimental models, clinical investigations and the effect of drugs. Related fields are broadly defined and include for instance, allergy and asthma, shock, pain, joint damage, skin disease as well as clinical trials of relevant drugs.
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