基础医学与临床 ›› 2014, Vol. 34 ›› Issue (1): 53-57.

• 研究论文 • 上一篇    下一篇

系统性红斑狼疮患者外周血miR-7的表达及其意义

李扬1,沈濂2,叶燕霞1,张烜1   

  1. 1. 中国医学科学院 北京协和医学院 北京协和医院
    2. 中国医学科学院 北京协和医学院 基础医学研究所
  • 收稿日期:2013-05-27 修回日期:2013-08-20 出版日期:2014-01-05 发布日期:2013-12-26
  • 通讯作者: 张烜 E-mail:zxpumch2003@hotmail.com
  • 基金资助:
    国家自然科学基金(地区基金);国家重点科技研发项目;中国国家高技术研究与发展项目(973项目)

The Expression and Clinical Significance of miR-7 In Peripheral Blood of Patients with Systemic Lupus Erythematosus

  • Received:2013-05-27 Revised:2013-08-20 Online:2014-01-05 Published:2013-12-26

摘要: 目的 研究microRNA-7(miR-7)在系统性红斑狼疮(SLE)患者外周血的表达及其意义。 方法 20例SLE患者和20例性别年龄匹配的健康对照者,荧光定量PCR检测PBMC、B细胞、T细胞和单核细胞中miR-7的表达以及靶基因PTEN的mRNA水平, 通过电转染方法将miR-7的前体Pre-miR? miR-7 Precursor/抑制剂Anti-miR? miR-7 Inhibitor转染至SLE患者B细胞中,流式细胞检测B细胞增值功能。应用生物信息学方法及双荧光素酶报告基因系统预测并验证miR-7的靶基因。 结果 SLE患者PBMC及B细胞中miR-7的表达显著高于健康对照(p<0.01)。PTEN是miR-7的一个靶基因,转染miR-7的前体至SLE患者B细胞可抑制PTEN表达(p<0.05),促进B细胞增殖(p<0.05),转染miR-7抑制体则可以促进PTEN表达(p<0.05),抑制B细胞增值(p<0.05)。结论miR-7参与了SLE的发病机制,调控PTEN的表达,并介导了SLE患者B细胞的增殖,是SLE潜在的治疗靶点。

关键词: 系统性红斑狼疮, 微小RNA-7, PTEN

Abstract: Objective To investigate the expression of microRNA-7(miR-7) in peripheral blood of patients with systemic lupus erythematosus(SLE) and its clinical significance. Methods Twenty patiens with SLE and twenty healthy controls(HCs) matched with age and gender were enrolled in this study. Real time quantitative PCR was used to detect the expression of miR-7 in peripheral blood mononuclear cells(PBMC) ,B cells,T cells and monocyte of SLE patients and HCs. PTEN mRNA expression levels were also evaluated by real time quantitative PCR. Flow cytometer was used to detect the proliferation ability of B cells, which transfected with miR-7 precursor or inhibitor and then elvaluated bioinformatics prediction and dual luciferase report gene assay system were performed to identify miR-7 targets. Results The expression of miR-7 in SLE patients was significantly higher than that in HCs(p<0.01). PTEN was one of target genes of miR-7. The B cell transfected with miR-7 precursor had reduced expression of PTEN and promoted proliferation of B cell(p<0.05).In contrast, the opposite effect was observed with the miR-7 inhibitor transfection. Conclusions: miR-7 was involved in the pathogenesis of SLE by regulating the PTEN expression and B cell proliferation.It may be a potential therapeutic target for SLE.

Key words: Systemic lupus erythematosus, microRNA-7, PTEN