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Mechanisms governing inflammasome activation assembly and pyroptosis induction

机译:控制炎症小体激活组装和诱导凋亡的机制

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摘要

Inflammasomes are multimeric protein complexes that regulate inflammatory responses and pyroptotic cell death to exert host defense against microbes. Intracellular pattern-recognition receptors such as nucleotide-binding domain and leucine-rich repeat receptors (NLRs) and absent in melanoma 2 like receptors (ALRs) assemble the inflammasome complexes in response to pathogens and danger or altered-self signals in the cell. Inflammasome sensors, in association with an adaptor protein—apoptosis-associated speck-like protein containing a caspase-activation and -recruitment domain (ASC)—activate inflammatory caspase-1 to enable the release of inflammatory cytokines and induce cell death, conferring host defense against pathogens. Beyond infectious diseases, the importance of inflammasomes is implicated in a variety of clinical conditions such as auto-inflammatory diseases, neuro-degeneration and metabolic disorders and the development of cancers. Understanding inflammasome activation and its molecular regulation can unveil therapeutic targets for controlling inflammasome-mediated disorders. In this review, we describe recent advances in inflammasome biology and discuss its activation, structural insights into inflammasome assembly and mechanisms for the execution of pyroptosis.
机译:炎症小体是调节炎症反应和焦细胞死亡的多聚体蛋白复合物,可对微生物发挥宿主防御作用。细胞内模式识别受体(例如核苷酸结合结构域和富含亮氨酸的重复受体(NLR))和黑色素瘤2样受体(ALR)中不存在,以响应病原体和细胞中的危险或自身信号改变来组装炎性体复合物。炎性体传感器与衔接蛋白(包含胱天蛋白酶激活和招聘结构域(ASC)的凋亡相关斑点样蛋白)结合,激活炎症caspase-1以释放炎性细胞因子并诱导细胞死亡,从而赋予宿主防御能力抵抗病原体。除感染性疾病外,炎症小体的重要性还涉及多种临床状况,例如自身炎症性疾病,神经退行性疾病和代谢性疾病以及癌症的发展。了解炎症小体的激活及其分子调控可以揭示控制炎症小体介导的疾病的治疗靶标。在这篇综述中,我们描述了炎症小体生物学的最新进展,并讨论了它的激活,对炎症小体组装的结构见解和执行烧伤的机制。

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