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MicroRNA‐126 regulates DNA methylation in CD4+ T cells and contributes to systemic lupus erythematosus by targeting DNA methyltransferase 1

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WOS被引频次:200
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成果类型:
期刊论文
作者:
Zhao, Sha;Wang, Yu;Liang, Yunsheng;Zhao, Ming;Long, Hai;Ding, Shu;Yin, Heng;Lu, Qianjin*
通讯作者:
Lu, Qianjin
作者机构:
[Lu, Qianjin] Cent S Univ, Xiangya Hosp 2, Dept Dermatol, Hunan Key Lab Med Epigenom, Changsha 410011, Hunan, Peoples R China.
[Lu, Qianjin] Cent S Univ, Xiangya Hosp 2, Dept Dermatol, Hunan Key Lab Med Epigenom, 139 Renmin Middle Rd, Changsha 410011, Hunan, Peoples R China.
通讯机构:
[Lu, Qianjin] Cent S Univ, Xiangya Hosp 2, Dept Dermatol, Hunan Key Lab Med Epigenom, 139 Renmin Middle Rd, Changsha 410011, Hunan, Peoples R China.
语种:
英文
期刊:
Arthritis & Rheumatism
ISSN:
1529-0131
年:
2011
卷:
63
期:
5
页码:
1376-1386
文献类别:
WOS:Article
所属学科:
ESI学科类别:临床医学;WOS学科类别:Rheumatology
入藏号:
基金类别:
National Natural Science Foundation of China [30730083, 30972745]; National Basic Research Program of China (973 Plan) [2009CB825605]
机构署名:
本校为第一且通讯机构
院系归属:
湘雅二医院(第二临床学院)
摘要:
To identify microRNA genes with abnormal expression in the CD4+ T cells of patients with systemic lupus erythematosus (SLE) and to determine the role of microRNA‐126 (miR‐126) in the etiology of SLE. MicroRNA expression patterns in CD4+ T cells from patients with SLE and healthy control subjects were analyzed by microRNA microarray and stem loop quantitative polymerase chain reaction (qPCR). Luciferase reporter gene assays were performed to identify miR‐126 targets. Dnmt1, CD11a, and CD70 messenger RNA and protein levels were determined by real‐time qPCR, Western blotting, and flow cytometry. CD11a, CD70, and EGFL7 promoter methylation levels were detected by bisulfite sequencing. IgG levels in T cell–B cell cocultures were determined by enzyme‐linked immunosorbent assay. The expression of 11 microRNA was significantly increased or decreased in CD4+ T cells from patients with SLE relative to that in CD4+ T cells from control subjects. Among these, miR‐126 was up‐regulated, and its degree of overexpression was inversely correlated with Dnmt1 protein levels. We demonstrated that miR‐126 directly inhibits Dnmt1 translation via interaction with its 3′–untranslated region, and that overexpression of miR‐126 in CD4+ T cells can significantly reduce Dnmt1 protein levels. The overexpression of miR‐126 in CD4+ T cells from healthy donors caused the demethylation and up‐regulation of genes encoding CD11a and CD70, thereby causing T cell and B cell hyperactivity. The inhibition of miR‐126 in CD4+ T cells from patients with SLE had the opposite effects. Expression of the miR‐126 host gene EGFL7 was also up‐regulated in CD4+ T cells from patients with SLE, possibly in a hypomethylation‐dependent manner. Our data suggest that miR‐126 regulates DNA methylation in CD4+ T cells and contributes to T cell autoreactivity in SLE by directly targeting Dnmt1.
参考文献:
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