Pruijn Ger J M
Department of Biochemistry, Radboud University Nijmegen, Nijmegen, The Netherlands.
Arthritis Res Ther. 2006;8(4):110. doi: 10.1186/ar1987.
Many intracellular macromolecular complexes that are involved in the production or degradation of RNAs are targeted by autoantibodies in systemic autoimmune diseases. RNA interference (RNAi) is a recently characterized gene silencing pathway by which specific mRNAs are either degraded or translationally suppressed. In a recent issue of Arthritis Research and Therapy, Andrew Jakymiw and colleagues reported that the enigmatic Su autoantigen complex contains key components of the RNAi machinery. Anti-Su autoantibodies from both human patients with rheumatic diseases and a mouse model of autoimmunity recognize the endonucleolytic Argonaute and Dicer proteins, both crucial enzymes of the RNAi pathway. These data raise the question of how the anti-Su response is triggered. So far, it is unknown whether molecular modifications may be involved, as has been proposed for other intracellular autoantigens. The implication of RNAi in anti-viral defence may suggest a role for virus infection in this process.
许多参与RNA产生或降解的细胞内大分子复合物是系统性自身免疫疾病中自身抗体的靶标。RNA干扰(RNAi)是一种最近被鉴定的基因沉默途径,通过该途径特定的mRNA被降解或翻译受到抑制。在最近一期的《关节炎研究与治疗》中,安德鲁·亚基米夫及其同事报告称,神秘的Su自身抗原复合物包含RNAi机制的关键成分。来自患有风湿性疾病的人类患者和自身免疫小鼠模型的抗Su自身抗体识别核酸内切酶Argonaute和Dicer蛋白,这两种都是RNAi途径的关键酶。这些数据提出了抗Su反应是如何触发的问题。到目前为止,尚不清楚是否像其他细胞内自身抗原那样,分子修饰可能参与其中。RNAi在抗病毒防御中的作用可能暗示病毒感染在这一过程中发挥作用。