van der Meer A D, Kamphuis M M J, Poot A A, Feijen J, Vermes I
Institute for Biomedical Technology and Department of Polymer Chemistry and Biomaterials, Faculty of Science and Technology, University of Twente, P.O. Box 217, 7500 AE Enschede, The Netherlands.
Int J Cell Biol. 2009;2009:532432. doi: 10.1155/2009/532432. Epub 2008 Dec 23.
Vascular endothelial cells have an extensive response to physiological levels of shear stress. There is evidence that the protein caveolin-1 is involved in the early phase of this response. In this study, caveolin-1 was downregulated in human endothelial cells by RNAi. When these cells were subjected to a shear stress of 15 dyn/cm(2) for 10 minutes, activation of Akt and ERK1/2 was significantly lower than in control cells. Moreover, activation of Akt and ERK1/2 in response to vascular endothelial growth factor was significantly lower in cells with low levels of caveolin-1. However, activation of integrin-mediated signaling during cell adhesion onto fibronectin was not hampered by lowered caveolin-1 levels. In conclusion, caveolin-1 is an essential component in the response of endothelial cells to shear stress. Furthermore, the results suggest that the role of caveolin-1 in this process lies in facilitating efficient VEGFR2-mediated signaling.
血管内皮细胞对生理水平的剪切应力有广泛反应。有证据表明,小窝蛋白-1参与了这一反应的早期阶段。在本研究中,通过RNA干扰下调人内皮细胞中的小窝蛋白-1。当这些细胞在15达因/平方厘米的剪切应力下作用10分钟时,Akt和ERK1/2的激活明显低于对照细胞。此外,在小窝蛋白-1水平较低的细胞中,对血管内皮生长因子反应时Akt和ERK1/2的激活也明显较低。然而,细胞黏附到纤连蛋白上时整合素介导的信号激活并未因小窝蛋白-1水平降低而受到阻碍。总之,小窝蛋白-1是内皮细胞对剪切应力反应中的重要组成部分。此外,结果表明小窝蛋白-1在此过程中的作用在于促进有效的VEGFR2介导的信号传导。