骨关节炎软骨细胞的新型程序性死亡.

BACKGROUND: Osteoarthritis is a common degenerative joint disease. Its pathogenesis is complex and has not been elucidated. However, studies have shown that the occurrence and development of osteoarthritis is related to the programmed death of chondrocytes. OBJECTIVE: To summarize the research progress in new programmed cell death in osteoarthritis chondrocytes. METHODS: “Osteoarthritis, Pyroptosis, Necroptosis, Ferroptosis, ROS, L-ROS, iron-overload” were used as English and Chinese search terms. Relevant articles on programmed cell death were searched in CNKI, WanFang, VIP, and PubMed. The search time was from July 2012 to July 2022. All included articles were summarized, concluded, and analyzed. RESULTS AND CONCLUSION: The relationship between pyroptosis and osteoarthritis has attracted much attention in recent years, and current research still focuses on NLRP3 inflammasome and lipopolysaccharides. The development of osteoarthritis has also been shown to be closely associated with receptor-interacting protein kinase 1 in studies concerning necroptosis, and receptor-interacting protein kinase 1 could be a potential target for the treatment of osteoarthritis. Ferroptosis is a recently discovered mode of cell death, which has been found to mediate chondrocyte death through iron overload and lipid peroxidation, but ferroptosis involves the expression and regulation of multiple genes via complex signaling pathways and mechanisms that are not yet fully elucidated. Pyroptosis, necroptosis, and ferroptosis have important roles in the occurrence and development of osteoarthritis, but their related pathways, genes, and miRNAs still need further study. [ABSTRACT FROM AUTHOR]