A possible role of HMGB1 in DNA demethylation in CD4+ T cells from patients with systemic lupus erythematosus.

Clinical & Developmental Immunology Pub Date : 2013-01-01 Epub Date: 2013-09-03 DOI:10.1155/2013/206298
Yaping Li, Chenghui Huang, Ming Zhao, Gongping Liang, Rong Xiao, Susan Yung, Tak Mao Chan, Qianjin Lu
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引用次数: 36

Abstract

The aberrant activity of CD4(+) T cells in patients with systemic lupus erythematosus (SLE) is associated with DNA hypomethylation of the regulatory regions in CD11a and CD70 genes. Our previous studies demonstrated that Gadd45a contributes to the development of SLE by promoting DNA demethylation in CD4(+) T cells. In this study, we identified proteins that bind to Gadd45a in CD4(+) T cells during SLE flare by using the method of co-immunoprecipitation and mass spectrometry, High mobility group box protein 1 (HMGB1) is one of identified proteins. Furthermore, gene and protein expression of HMGB1 was significantly increased in SLE CD4(+) T cells compared to controls, and HMGB1 mRNA was correlated with CD11a and CD70 mRNA. A significant, positive correlation was found between HMGB1 mRNA and SLEDAI for SLE patients. Our data demonstrate that HMGB1 binds to Gadd45a and may be involved in DNA demethylation in CD4(+) T cells during lupus flare.

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HMGB1在系统性红斑狼疮患者CD4+ T细胞DNA去甲基化中的可能作用
系统性红斑狼疮(SLE)患者CD4(+) T细胞的异常活性与CD11a和CD70基因调控区DNA低甲基化有关。我们之前的研究表明,Gadd45a通过促进CD4(+) T细胞中的DNA去甲基化而促进SLE的发展。在本研究中,我们利用共免疫沉淀和质谱法鉴定了SLE发作期间CD4(+) T细胞中与Gadd45a结合的蛋白,高迁移率组框蛋白1 (HMGB1)是鉴定的蛋白之一。此外,与对照组相比,SLE CD4(+) T细胞中HMGB1基因和蛋白表达显著升高,HMGB1 mRNA与CD11a和CD70 mRNA相关。HMGB1 mRNA与SLE患者SLEDAI呈显著正相关。我们的数据表明,HMGB1与Gadd45a结合,并可能参与狼疮发作期间CD4(+) T细胞的DNA去甲基化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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