Long Li, Guo Hongmei, Chen Xixi, Liu Yan, Wang Ruyi, Zheng Xiaomei, Huang Xiaobo, Zhou Qiao, Wang Yi
Department of Rheumatology and Immunology, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, China.
Zunyi Medical University, Zunyi, China.
Front Physiol. 2022 Oct 4;13:1036515. doi: 10.3389/fphys.2022.1036515. eCollection 2022.
Rheumatoid arthritis (RA) is a chronic, systemic disease of unknown etiology. The primary manifestation of RA is inflammatory synovitis, which eventually leads to deformity and functional loss. Ferroptosis is a non-apoptosis form of cell death that depends on intracellular iron accumulation. This leads to an increase in reactive oxygen species (ROS) induced-lipid peroxidation. The underlying mechanisms of ferroptosis are System Xc- and Glutathione metabolism, regulation of glutathione peroxidase 4 activity, and ROS generation. Recent studies have shown an association between the pathogenesis of RA and ferroptosis, suggesting the involvement of ferroptosis in the onset and progression of RA. In this review, we have focused on the mechanism of ferroptosis and its association with RA pathogenesis. Further, we discuss the status of therapeutics targeting ferroptosis in the treatment of patients with RA. Targeting ferroptosis could be a potential therapeutic approach for RA treatment.
类风湿关节炎(RA)是一种病因不明的慢性全身性疾病。RA的主要表现为炎症性滑膜炎,最终导致畸形和功能丧失。铁死亡是一种非凋亡形式的细胞死亡,它依赖于细胞内铁的积累。这会导致活性氧(ROS)诱导的脂质过氧化增加。铁死亡的潜在机制是系统Xc-和谷胱甘肽代谢、谷胱甘肽过氧化物酶4活性的调节以及ROS的产生。最近的研究表明RA的发病机制与铁死亡之间存在关联,提示铁死亡参与了RA的发病和进展。在这篇综述中,我们重点关注了铁死亡的机制及其与RA发病机制的关联。此外,我们讨论了针对铁死亡的治疗方法在RA患者治疗中的现状。靶向铁死亡可能是RA治疗的一种潜在治疗方法。