miR-146a and Kruppel-like factor 4 form a feedback loop to participate in vascular smooth muscle cell proliferation

被引:154
作者
Sun, Shao-guang [1 ]
Zheng, Bin [1 ]
Han, Mei [1 ]
Fang, Xin-mei [1 ]
Li, Hui-xuan [1 ]
Miao, Sui-bing [1 ]
Su, Ming [1 ]
Han, Yi [1 ]
Shi, Hui-jing [1 ]
Wen, Jin-kun [1 ]
机构
[1] Hebei Med Univ, Dept Biochem & Mol Biol, Key Lab Neural & Vasc Biol, China Adm Educ, Shijiazhuang 050017, Peoples R China
关键词
Kruppel-like factor 4; microRNA; miR-146a; proliferation; vascular smooth muscle cells; RETINOIC ACID; EXPRESSION; GROWTH; KRUPPEL-LIKE-FACTOR-4; INHIBITION; INDUCTION; GENE;
D O I
10.1038/embor.2010.172
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs are phenotypic regulators of vascular smooth muscle cells (VSMCs). In this paper, we demonstrate that miR-146a targets the Kruppel-like factor 4 (KLF4) 3'-untranslated region and has an important role in promoting VSMC proliferation in vitro and vascular neointimal hyperplasia in vivo. Silencing of miR-146a in VSMCs increases KLF4 expression, whereas overexpression of miR-146a decreases KLF4 levels. Furthermore, we demonstrate that KLF4 competes with Kruppel-like factor 5 (KLF5) to bind to and regulate the miR-146a promoter, and that KLF4 and KLF5 exert opposing effects on the miR-146a promoter. Overexpression of KLF4 in VSMCs decreases miR-146a transcription levels. By using both gain-of-function and loss-of-function approaches, we found that miR-146a promotes VSMC proliferation in vitro. Transfection of antisense miR-146a oligonucleotide into balloon-injured rat carotid arteries markedly decreased neointimal hyperplasia. These findings suggest that miR-146a and KLF4 form a feedback loop to regulate each other's expression and VSMC proliferation.
引用
收藏
页码:56 / 62
页数:7
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