Hung T, Pratt G A, Sundararaman B, Townsend M J, Chaivorapol C, Bhangale T, Graham R R, Ortmann W, Criswell L A, Yeo G W, Behrens T W
Genentech, South San Francisco, CA 94080, USA.
Department of Cellular and Molecular Medicine, Institute for Genomic Medicine, Stem Cell Program, University of California at San Diego, Sanford Consortium for Regenerative Medicine, 2880 Torrey Pines Scenic Drive, La Jolla, CA 92037, USA.
Science. 2015 Oct 23;350(6259):455-9. doi: 10.1126/science.aac7442. Epub 2015 Sep 17.
Autoantibodies target the RNA binding protein Ro60 in systemic lupus erythematosus (SLE) and Sjögren's syndrome. However, it is unclear whether Ro60 and its associated RNAs contribute to disease pathogenesis. We catalogued the Ro60-associated RNAs in human cell lines and found that among other RNAs, Ro60 bound an RNA motif derived from endogenous Alu retroelements. Alu transcripts were induced by type I interferon and stimulated proinflammatory cytokine secretion by human peripheral blood cells. Ro60 deletion resulted in enhanced expression of Alu RNAs and interferon-regulated genes. Anti-Ro60-positive SLE immune complexes contained Alu RNAs, and Alu transcripts were up-regulated in SLE whole blood samples relative to controls. These findings establish a link among the lupus autoantigen Ro60, Alu retroelements, and type I interferon.
自身抗体在系统性红斑狼疮(SLE)和干燥综合征中靶向RNA结合蛋白Ro60。然而,尚不清楚Ro60及其相关RNA是否参与疾病发病机制。我们对人类细胞系中与Ro60相关的RNA进行了编目,发现在其他RNA中,Ro60结合了源自内源性Alu逆转录元件的RNA基序。Alu转录本由I型干扰素诱导,并刺激人外周血细胞分泌促炎细胞因子。Ro60缺失导致Alu RNA和干扰素调节基因的表达增强。抗Ro60阳性的SLE免疫复合物含有Alu RNA,并且相对于对照,SLE全血样本中Alu转录本上调。这些发现建立了狼疮自身抗原Ro60、Alu逆转录元件和I型干扰素之间的联系。