Espinosa Alexander, Zhou Wei, Ek Monica, Hedlund Malin, Brauner Susanna, Popovic Karin, Horvath Linn, Wallerskog Therese, Oukka Mohamed, Nyberg Filippa, Kuchroo Vijay K, Wahren-Herlenius Marie
Rheumatology Unit, Department of Medicine, Karolinska Institutet at Danderyd Hospital, Karolinska Institutet, S-17176 Stockholm, Sweden.
J Immunol. 2006 May 15;176(10):6277-85. doi: 10.4049/jimmunol.176.10.6277.
Patients affected by Sjögren's syndrome and systemic lupus erythematosus (SLE) carry autoantibodies to an intracellular protein denoted Ro52. Although the serologic presence of Ro52 autoantibodies is used clinically for diagnostic purposes, the function of the protein or why it is targeted as an autoantigen in several rheumatic conditions has not been elucidated. In this study, we show that the expression of Ro52 is significantly increased in PBMC of patients with Sjögren's syndrome and SLE, and demonstrate that Ro52 is a RING-dependent E3 ligase involved in ubiquitination. Overexpression of Ro52, but not of Ro52 lacking the RING domain, in a mouse B cell line lead to decreased growth in steady state and increased cell death after activation via the CD40 pathway. The role of Ro52 in activation-mediated cell death was further confirmed as a reduction in Ro52 expression restored cell viability. These findings suggest that the increased expression of the Ro52 autoantigen in patients may be directly involved in the reduced cellular proliferation and increased apoptotic cell death observed in Sjögren's syndrome and SLE, and may thus contribute to the autoantigenic load and induction of autoimmune B and T cell responses observed in rheumatic patients.
患有干燥综合征和系统性红斑狼疮(SLE)的患者体内携带针对一种名为Ro52的细胞内蛋白的自身抗体。尽管Ro52自身抗体的血清学存在在临床上用于诊断目的,但该蛋白的功能或为何在几种风湿性疾病中被作为自身抗原靶向尚未阐明。在本研究中,我们表明干燥综合征和SLE患者外周血单个核细胞(PBMC)中Ro52的表达显著增加,并证明Ro52是一种参与泛素化的依赖RING的E3连接酶。在小鼠B细胞系中过表达Ro52而非缺乏RING结构域的Ro52,导致稳态下生长减少以及通过CD40途径激活后细胞死亡增加。Ro52在激活介导的细胞死亡中的作用进一步得到证实,因为Ro52表达的降低恢复了细胞活力。这些发现表明,患者体内Ro52自身抗原表达的增加可能直接参与了干燥综合征和SLE中观察到的细胞增殖减少和凋亡性细胞死亡增加,因此可能导致风湿性患者中观察到的自身抗原负荷以及自身免疫性B和T细胞反应的诱导。