Amano Tetsuya, Yamasaki Satoshi, Yagishita Naoko, Tsuchimochi Kaneyuki, Shin Hiroshi, Kawahara Ko-ichi, Aratani Satoko, Fujita Hidetoshi, Zhang Lei, Ikeda Rie, Fujii Ryoji, Miura Naoki, Komiya Setsuro, Nishioka Kusuki, Maruyama Ikuro, Fukamizu Akiyoshi, Nakajima Toshihiro
Department of Genome Science, Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Kanagawa 216-8512, Japan.
Genes Dev. 2003 Oct 1;17(19):2436-49. doi: 10.1101/gad.1096603. Epub 2003 Sep 15.
Rheumatoid arthritis (RA) is one of the most critical articular diseases with synovial hyperplasia followed by impairment of quality of life. However, the mechanism(s) that regulates synovial cell outgrowth is not fully understood. To clarify its mechanism(s), we carried out immunoscreening by using antirheumatoid synovial cell antibody and identified and cloned "Synoviolin/Hrd1", an E3 ubiquitin ligase. Synoviolin/Hrd1 was highly expressed in the rheumatoid synovium, and mice overexpressing this enzyme developed spontaneous arthropathy. Conversely, synoviolin/hrd1(+/-) mice were resistant to collagen-induced arthritis by enhanced apoptosis of synovial cells. We conclude that Synoviolin/Hrd1 is a novel causative factor for arthropathy by triggering synovial cell outgrowth through its antiapoptotic effects. Our findings provide a new pathogenetic model of RA and suggest that Synoviolin/Hrd1 could be targeted as a therapeutic strategy for RA.
类风湿性关节炎(RA)是最严重的关节疾病之一,其特征为滑膜增生,进而影响生活质量。然而,调节滑膜细胞生长的机制尚未完全明确。为阐明其机制,我们使用抗类风湿滑膜细胞抗体进行免疫筛选,鉴定并克隆了一种E3泛素连接酶“滑膜素/Hrd1”。滑膜素/Hrd1在类风湿滑膜中高表达,过表达该酶的小鼠会发生自发性关节病。相反,滑膜素/hrd1(+/-)小鼠由于滑膜细胞凋亡增强,对胶原诱导的关节炎具有抗性。我们得出结论,滑膜素/Hrd1是关节病的一个新致病因素,它通过抗凋亡作用触发滑膜细胞生长。我们的研究结果提供了一种新的RA发病机制模型,并表明滑膜素/Hrd1可作为RA的治疗靶点。