新生内膜
新生内膜增生
血管平滑肌
增生
细胞周期蛋白D1
癌症研究
细胞生长
调节器
转染
细胞生物学
医学
内膜增生
内科学
化学
生物
平滑肌
细胞培养
再狭窄
癌症
细胞周期
支架
生物化学
基因
遗传学
作者
Yu Zhang,Yong Li,Chao Liu,Chan-juan Nie,Xinhua Zhang,Cuiying Zheng,Wen Jiang,Wei‐Na Yin,Minghui Ren,Yu‐Xin Jin,Shufeng Liu,Bin Zheng,Jin‐Kun Wen
摘要
Abstract Objectives The formation of vascular neointima is mainly related to impairment of the vascular endothelial barrier and abnormal proliferation and migration of smooth muscle cells. The objective of this study was to investigate whether miR‐29a exerts any promoting effect on the vascular neointimal hyperplasia and if so, its mechanism. Materials and methods RT ‐ qPCR was performed to determine expression of miR‐29a in vascular smooth muscle cells ( VSMC ) and vascular neointimal hyperplasia. To further understand its role, we restored its expression in VSMC s by transfection with miR‐29a mimics or inhibitors. Effects of miR‐29a on cell proliferation were also determined. Results In this study, we used two kinds of model to observe the role of miR‐29a in neointimal hyperplasia induced by carotid ligation or balloon injury. The major findings were that: (i) miR‐29a overexpression promoted neointimal hyperplasia induced by carotid ligation; (ii) miR‐29a increased proliferation of VSMC s, one aspect of which was by targeting expression of Ying and yang 1 protein ( YY 1), a negative regulator of Cyclin D1. A further aspect, was by increasing expression of Krüppel‐like factor 5, a positive regulator of Cyclin D1, thereby allowing formation a synergistic effect. (iii) Tongxinluo ( TXL ), a traditional Chinese medicine reduced neointimal formation in ligated vessels by inhibiting VSMC proliferation and migration. Conclusions These findings provide a new molecular mechanism of TXL in decreasing neointima hyperplasia.
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