Lv Shuangyu, Wang Honggang, Li Xiaotian
Institute of Biomedical Informatics, Bioinformatics Center, School of Basic Medical Sciences, Henan University, Kaifeng, China.
Front Cell Dev Biol. 2021 Mar 16;9:634118. doi: 10.3389/fcell.2021.634118. eCollection 2021.
Autophagy is an important and conserved cellular pathway in which cells transmit cytoplasmic contents to lysosomes for degradation. It plays an important role in maintaining the balance of cell composition synthesis, decomposition and reuse, and participates in a variety of physiological and pathological processes. The nucleotide-binding oligomerization domain-like receptor family, pyrin domain-containing 3 (NLRP3) inflammasome can induce the maturation and secretion of Interleukin-1 beta (IL-1β) and IL-18 by activating caspase-1. It is involved in many diseases. In recent years, the interplay between autophagy and NLRP3 inflammasome has been reported to contribute to many diseases including metabolic disorders related diseases. In this review, we summarized the recent studies on the interplay between autophagy and NLRP3 inflammasome in metabolic disorders to provide ideas for the relevant basic research in the future.
自噬是一种重要且保守的细胞途径,细胞通过该途径将细胞质内容物输送到溶酶体进行降解。它在维持细胞成分合成、分解和再利用的平衡中发挥重要作用,并参与多种生理和病理过程。含核苷酸结合寡聚化结构域样受体家族吡啉结构域3(NLRP3)炎性小体可通过激活半胱天冬酶-1诱导白细胞介素-1β(IL-1β)和IL-18的成熟和分泌。它与许多疾病有关。近年来,据报道自噬与NLRP3炎性小体之间的相互作用导致了包括代谢紊乱相关疾病在内的许多疾病。在本综述中,我们总结了自噬与NLRP3炎性小体在代谢紊乱中相互作用的最新研究,为未来相关基础研究提供思路。