Kong Ruixue, Peng Lijun, Bao Honggang, Sun Lulu, Feng Yan, Li Hua, Wang Dashan
College of Life Sciences, Shandong Normal University, Jinan, 250014, Shandong, China.
Department of Gastroenterology, Linyi People's Hospital, Linyi, 276000, Shandong, China.
Inflamm Res. 2024 Dec;73(12):2249-2261. doi: 10.1007/s00011-024-01961-x. Epub 2024 Oct 26.
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.
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).
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).
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.
G蛋白是哺乳动物中一类重要的信号转导分子。G蛋白可与G蛋白偶联受体(GPCRs)结合,将细胞外刺激信号传递至细胞内反应,进而调节一系列生物学功能。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。我们之前的研究表明,Gαq在调节T细胞存活和T细胞分化中起重要作用。炎性小体是多蛋白复合物,在调节先天性炎症反应中起关键作用。NLRP3炎性小体是目前研究最广泛的炎性小体。
我们发现Gαq抑制巨噬细胞中NLRP3炎性小体的激活,Gαq在脂多糖诱导的脓毒症小鼠模型中也抑制NLRP3炎性小体的激活。Gαq可定位于线粒体,且维持线粒体稳态需要Gαq。Gαq通过调节线粒体活性氧(mtROS)来调节NLRP3炎性小体的激活。
我们发现Gαq抑制巨噬细胞中NLRP3炎性小体的激活,Gαq在脂多糖诱导的脓毒症小鼠模型中也抑制NLRP3炎性小体的激活。Gαq可定位于线粒体,且维持线粒体稳态需要Gαq。Gαq通过调节线粒体活性氧(mtROS)来调节NLRP3炎性小体的激活。
我们的结果表明,Gαq通过调节线粒体ROS生成来调节NLRP3炎性小体的激活。我们的研究为NLRP3炎性小体的激活提供了新的机制见解。由于已证明NLRP3炎性小体在许多疾病如阿尔茨海默病、癌症和炎症性肠病的发病机制中起重要作用,Gαq未来可能成为这些疾病的新型药物靶点。