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炎性小体激活的细胞生物学

Cell biology of inflammasome activation.

作者信息

Pandey Abhimanu, Shen Cheng, Feng Shouya, Man Si Ming

机构信息

Department of Immunology and Infectious Disease, The John Curtin School of Medical Research, The Australian National University, Canberra, Australia.

Department of Immunology and Infectious Disease, The John Curtin School of Medical Research, The Australian National University, Canberra, Australia.

出版信息

Trends Cell Biol. 2021 Nov;31(11):924-939. doi: 10.1016/j.tcb.2021.06.010. Epub 2021 Jul 17.

Abstract

Organelles are critical structures in mediating the assembly and activation of inflammasomes in mammalian cells, resulting in inflammation and cell death. Assembly of inflammasomes can occur at the mitochondria, endoplasmic reticulum, nucleus, trans-Golgi network, or pathogen surface, facilitated by the overarching architecture of the cytoskeleton. NLRP3 and Pyrin inflammasome sensors may form smaller speckles and converge on a single larger speck at the microtubule-organizing center (MTOC). This signaling hub activates multiple mammalian inflammatory and apoptotic caspases, cytokine substrates, the pore-forming protein gasdermin D, and the plasma membrane rupture protein ninjurin-1 (NINJ1), allowing pyroptosis, cellular disintegration, and inflammation to ensue. In this review, we highlight the role of mammalian cell types and organellar architectures in executing inflammasome responses.

摘要

细胞器是介导哺乳动物细胞中炎性小体组装和激活的关键结构,可导致炎症和细胞死亡。炎性小体的组装可发生在线粒体、内质网、细胞核、反式高尔基体网络或病原体表面,细胞骨架的总体结构对此起到促进作用。NLRP3和 Pyrin炎性小体传感器可能形成较小的斑点,并在微管组织中心(MTOC)汇聚成一个更大的斑点。这个信号枢纽激活多种哺乳动物炎性和凋亡半胱天冬酶、细胞因子底物、成孔蛋白gasdermin D和质膜破裂蛋白ninjurin-1(NINJ1),从而引发细胞焦亡、细胞解体和炎症。在本综述中,我们强调了哺乳动物细胞类型和细胞器结构在执行炎性小体反应中的作用。

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