Wang Xing, Fan Danping, Cao Xiaoxue, Ye Qinbin, Wang Qiong, Zhang Mengxiao, Xiao Cheng
School of Clinical Medicine, China-Japan Friendship Hospital, Beijing University of Chinese Medicine, Beijing 100029, China.
Institute of Clinical Medicine, China-Japan Friendship Hospital, Beijing 100029, China.
Antioxidants (Basel). 2022 Jun 13;11(6):1153. doi: 10.3390/antiox11061153.
Rheumatoid arthritis (RA) is an inflammatory disease that begins with a loss of tolerance to modified self-antigens and immune system abnormalities, eventually leading to synovitis and bone and cartilage degradation. Reactive oxygen species (ROS) are commonly used as destructive or modifying agents of cellular components or they act as signaling molecules in the immune system. During the development of RA, a hypoxic and inflammatory situation in the synovium maintains ROS generation, which can be sustained by increased DNA damage and malfunctioning mitochondria in a feedback loop. Oxidative stress caused by abundant ROS production has also been shown to be associated with synovitis in RA. The goal of this review is to examine the functions of ROS and related molecular mechanisms in diverse cells in the synovial microenvironment of RA. The strategies relying on regulating ROS to treat RA are also reviewed.
类风湿性关节炎(RA)是一种炎症性疾病,始于对修饰自身抗原的耐受性丧失和免疫系统异常,最终导致滑膜炎以及骨骼和软骨退化。活性氧(ROS)通常用作细胞成分的破坏或修饰剂,或者在免疫系统中充当信号分子。在RA的发展过程中,滑膜中的缺氧和炎症状态维持ROS的产生,这可以通过DNA损伤增加和线粒体功能异常在反馈回路中持续存在。大量产生ROS引起的氧化应激也已被证明与RA中的滑膜炎有关。本综述的目的是研究RA滑膜微环境中不同细胞中ROS的功能及相关分子机制。还综述了依靠调节ROS来治疗RA的策略。