Wang Nanping, Miao Hui, Li Yi-Shuan, Zhang Peng, Haga Jason H, Hu Yingli, Young Angela, Yuan Suli, Nguyen Phu, Wu Chia-Ching, Chien Shu
Department of Bioengineering, Whitaker Institute of Biomedical Engineering, University of California-San Diego, La Jolla, CA 92093-0412, USA.
Biochem Biophys Res Commun. 2006 Mar 24;341(4):1244-51. doi: 10.1016/j.bbrc.2006.01.089. Epub 2006 Jan 30.
Flow patterns in blood vessels contribute to focal distribution of atherosclerosis; the underlying mechanotransduction pathways remain to be investigated. We demonstrate that different flow patterns elicit distinct responses of Krüppel-like factor-2 (KLF2) in endothelial cells (ECs) in vitro and in vivo. While pulsatile flow with a significant forward direction induced sustained expression of KLF2 in cultured ECs, oscillatory flow with little forward direction caused prolonged suppression after a transient induction. The suppressive effect of oscillatory flow was Src-dependent. Immunohistochemical studies on ECs at arterial branch points revealed that KLF2 protein levels were related to local hemodynamics. Such flow-associated expression patterns were also demonstrated in a rat aortic restenosis model. Inhibition of KLF2 with siRNA sensitized ECs to oxidized LDL-induced apoptosis, indicating a protective role of KLF2. In conclusion, differential regulation of KLF2 may mediate the distinct vascular effects induced by various patterns of shear stress.
血管中的血流模式导致动脉粥样硬化的局灶性分布;其潜在的机械转导途径仍有待研究。我们证明,不同的血流模式在体外和体内的内皮细胞(ECs)中引发Krüppel样因子2(KLF2)的不同反应。虽然具有明显向前方向的脉动流在培养的ECs中诱导KLF2持续表达,但向前方向很小的振荡流在短暂诱导后导致长时间抑制。振荡流的抑制作用依赖于Src。对动脉分支点处ECs的免疫组织化学研究表明,KLF2蛋白水平与局部血流动力学有关。在大鼠主动脉再狭窄模型中也证实了这种与血流相关的表达模式。用siRNA抑制KLF2使ECs对氧化低密度脂蛋白诱导的凋亡敏感,表明KLF2具有保护作用。总之,KLF2的差异调节可能介导了由各种剪切应力模式诱导的不同血管效应。