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类风湿关节炎患者 CD4(+) T 细胞中 CD40L 的去甲基化。

CD40L demethylation in CD4(+) T cells from women with rheumatoid arthritis.

机构信息

Department of Dermatology, Second Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.

出版信息

Clin Immunol. 2012 Oct;145(1):13-8. doi: 10.1016/j.clim.2012.07.006. Epub 2012 Jul 21.

Abstract

We have previously demonstrated that DNA demethylation of CD40L on the X chromosome is responsible for female susceptibility to systemic lupus erythematosus (SLE). It is unknown whether aberrant methylation of the CD40L gene also contributes to the higher incidence of rheumatoid arthritis (RA) in females. In this study, we used real-time RT-PCR and flow cytometry to compare CD40L expression levels, and bisulfite sequencing to assess the methylation status of the CD40L promoter region. The results show that CD40L is upregrulated in CD4(+) T cells of female patients with RA. In addition, the CD40L promoter region in CD4(+) T cells from female RA patients was found to be demethylated, which corresponded with increased CD40L mRNA expression. These findings suggest that DNA demethylation contributes to CD40L expression in RA CD4(+) T cells and may in part explain the female preponderance of this disease.

摘要

我们之前已经证明,X 染色体上 CD40L 的 DNA 去甲基化是女性易患系统性红斑狼疮(SLE)的原因。目前尚不清楚 CD40L 基因的异常甲基化是否也导致女性类风湿关节炎(RA)发病率更高。在这项研究中,我们使用实时 RT-PCR 和流式细胞术比较了 CD40L 的表达水平,并使用亚硫酸氢盐测序评估了 CD40L 启动子区域的甲基化状态。结果表明,RA 女性患者的 CD4+T 细胞中 CD40L 表达上调。此外,我们发现 RA 女性患者的 CD4+T 细胞中 CD40L 启动子区域发生了去甲基化,这与 CD40L mRNA 表达增加相对应。这些发现表明,DNA 去甲基化有助于 RA CD4+T 细胞中 CD40L 的表达,这可能部分解释了这种疾病在女性中的高发。

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