Fujiwara K
Cardiovascular Research Institute, University of Rochester Medical Center, Rochester, NY 14642, USA.
J Intern Med. 2006 Apr;259(4):373-80. doi: 10.1111/j.1365-2796.2006.01623.x.
Endothelial cells are known to respond to mechanical forces such as fluid shear stress and cyclic stretch, but elucidating the mechanism for mechanosensing has been difficult. Experimental data indicate that there are probably several sensing mechanisms. We have recently proposed a novel mechanoresponse mechanism that involves platelet endothelial cell adhesion molecule-1 (PECAM-1). When endothelial cells are stimulated by fluid shear stress, PECAM-1 is tyrosine phosphorylated and activates the extracellular signal-regulated kinase 1 and 2 (ERK1/2) signalling cascade. The same signalling events occurred when we applied pulling force directly on PECAM-1 on the endothelial cell surface using magnetic beads coated with antibodies against the external domain of PECAM-1. These results appear to indicate that PECAM-1 is a mechanotransduction molecule. To our knowledge, this is the first mammalian molecule that is shown to respond to mechanical force directly exerted to it.
已知内皮细胞会对诸如流体剪切应力和周期性拉伸等机械力作出反应,但阐明机械传感机制一直很困难。实验数据表明可能存在多种传感机制。我们最近提出了一种涉及血小板内皮细胞黏附分子-1(PECAM-1)的新型机械反应机制。当内皮细胞受到流体剪切应力刺激时,PECAM-1会发生酪氨酸磷酸化,并激活细胞外信号调节激酶1和2(ERK1/2)信号级联反应。当我们使用包被有抗PECAM-1胞外域抗体的磁珠直接对内皮细胞表面的PECAM-1施加拉力时,也会发生同样的信号事件。这些结果似乎表明PECAM-1是一种机械转导分子。据我们所知,这是第一个被证明能直接对施加于其上的机械力作出反应的哺乳动物分子。