Department of Laboratory Medicine, Central South University, Changsha, Hunan, People's Republic of China; Department of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Department of Laboratory Medicine, Central South University, Changsha, Hunan, People's Republic of China; Department of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Int Immunopharmacol. 2022 Jul;108:108719. doi: 10.1016/j.intimp.2022.108719. Epub 2022 Mar 26.
As an intracellular polyprotein complex, the NLRP3 inflammasome is activated by NLRP3 perceiving pathogen-related molecular patterns, damage-related molecular patterns(DAMPs), which will result in the secretion of the caspase1-dependent pro-inflammatory cytokines IL1β and IL18, and the cleavage of GSDMD-mediated pyroptosis. Therefore, inflammasome signaling is tightly regulated. Intracellular and extracellular mitochondria DNA (mtDNA) play different roles in activating the NLRP3 inflammasome. Intracellular mtDNA is easily oxidized and transferred to the cytoplasm, and directly binds to NLRP3 to activate NLRP3 inflammasome, the extracellular mtDNA is involved in the priming and activation of NLRP3 inflammasome as a DAMP; which is related to the occurrence and development of plentiful diseases. In this paper, we will discuss how mitochondrial DNA activates the NLRP3 inflammasome and how the process of activating NLRP3 inflammasome by mtDNA interacts with other NLRP3 inflammasome activation models.
作为一种细胞内多蛋白复合物,NLRP3 炎性小体被 NLRP3 识别病原体相关分子模式(PAMPs)和损伤相关分子模式(DAMPs)激活,进而导致依赖 caspase1 的促炎细胞因子 IL1β 和 IL18 的分泌,以及 GSDMD 介导的细胞焦亡的裂解。因此,炎性小体信号受到严格调控。细胞内和细胞外线粒体 DNA(mtDNA)在激活 NLRP3 炎性小体方面发挥着不同的作用。细胞内 mtDNA 容易氧化并转移到细胞质中,直接与 NLRP3 结合激活 NLRP3 炎性小体,细胞外 mtDNA 作为 DAMPs 参与 NLRP3 炎性小体的初始激活;这与大量疾病的发生和发展有关。本文将讨论 mtDNA 如何激活 NLRP3 炎性小体,以及 mtDNA 激活 NLRP3 炎性小体的过程如何与其他 NLRP3 炎性小体激活模型相互作用。