内含子源性miRNA通过转录因子AP1调节内皮型一氧化氮合酶表达及血管内皮细胞增殖作用
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国家自然科学基金项目(81373403);广西硕士研究生科研创新项目(YCSZ2013031)


Intronic miRNA Regulates Human Endothelial Nitric Oxide Synthase Gene and Proliferation of Endothelial Cells by the Transcription Factor AP1
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    目的 前期工作发现,内皮型一氧化氮合酶(eNOS)第4内含子的27碱基重复子产生相应27-nt miRNA,并对eNOS的转录和表达有负反馈调节作用。进一步探讨该内含子源性27-nt miRNA对内皮型一氧化氮合酶基因调节的分子机制及血管内皮细胞增殖相关转录因子AP1的作用机制。方法 应用MTT法检测人脐静脉内皮细胞(HUVEC)的增殖抑制率;细胞划痕实验检测HUVEC迁移能力;免疫组织化学方法检测内皮细胞中eNOS和AP1蛋白表达水平;进一步用Western Blot检测27-nt miRNA表达相关情况及细胞核转录因子eNOS表达情况。结果 27-nt miRNA对HUVEC增殖具有强烈抑制作用 (P<0.05);27-nt miRNA对HUVEC迁移具有显著抑制作用(P<0.05);27-nt miRNA显著降低eNOS和AP1蛋白表达(P<0.05);27-nt miRNA通过负调控AP1降低eNOS蛋白表达(P<0.05)。结论 27-nt miRNA显著抑制eNOS和AP1蛋白表达,AP1在27-nt miRNA对eNOS表达调节中起重要作用。

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    Aim We previously reported that endothelial nitric oxide synthase (eNOS) intron 4 of 27 bp repeat promoter to produce the corresponding 27-nt miRNA, which regulated expression of eNOS. This study was to investigate an intronic miRNA regulated expression of the human eNOS gene and proliferation of endothelial cells by mechanism related to the transcription factor AP1. Methods The endothelial cells proliferation inhibition rate was detected by MTT assay. Migration ability of endothelial cells was measured by scratch wound model in vitro. The protein expression level of AP1 and eNOS were detected by Western Blot. Results Overexpression of 27-nt miRNA significantly inhibited the endothelial cells proliferation (P<0.05). Overexpression of 27-nt miRNA significantly inhibited HUVEC migration (P<0.05). Overexpression of 27-nt miRNA significantly decreased AP1 and eNOS protein expression (P<0.05). Overexpression of 27-nt miRNA significantly decreased eNOS protein expression by the transcription factor AP1. Conclusions The 27nt-miRNA suppresses eNOS gene expression and AP1 expression in endothelial cells. 27-nt miRNA regulated expression of the eNOS by the transcription factor AP1.

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李玉媚,王 辉,张文宇,陈 伟,胡 楠,欧和生.内含子源性miRNA通过转录因子AP1调节内皮型一氧化氮合酶表达及血管内皮细胞增殖作用[J].中国动脉硬化杂志,2014,22(07):649~654.

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  • 收稿日期:2013-12-03
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