Effects of Biomechanical Stress on Gene Regulation in Vascular Cells
The vascular vessel wall is constantly exposed to biomechanical forces, such as shear and tensile stress. Biomechanical forces are important for several physiological and pathological processes and have been shown to regulate a number of fundamental vascular functions, such as vascular tone and remodeling processes. The aim of the present thesis was to study the effects of biomechanical forces on the vessel wall. Intact human conduit vessels were exposed to normal or high intraluminal pressure, or low or high shear stress in combination with a physiological level of the other factor in a unique vascular ex vivo perfusion model, developed in our laboratory. Global gene expression profiling was performed with microarray technology of endothelial cells from stimulated vessels. Biomechanical forces were found to regulate a large number of genes. The fraction of genes that responded to both pressure and shear stimulation was surprisingly low, which indicates that the two different stimuli induce distinct gene expression response patterns. Further, these results suggest that the endothelium has the capacity to discriminate between shear stress and pressure stimulation. Detection and quantification of changes in gene expression require valid and reliable endogenous references genes. Therefore, the appropriateness of ten reference genes for studies of biomechanically stimulated endothelium was evaluated by microarray technology and real-time RT-PCR. Shear stress plays an essential role in regulation of vascular tone and remodeling, and P2 receptors have been suggested to be mediators of some of these effects. We therefore studied the effects of shear stress on P2 receptor expression in intact human vessels. In the endothelium, no significant regulation of P2 receptor mRNA levels was observed. However, in smooth muscle cells, high shear stress decreased mRNA expression of the contractile P2X1 receptor and increased the mitogenic P2Y2 and P2Y6 receptors. These findings were consistent at the protein level with Western blot analysis and morphologically with immunohistochemistry. This suggests that the shear force can be transmitted to the underlying smooth muscle cells. The interplay of shear stress and inflammatory stress on urokinase-type plasminogen activator (u-PA) and plasminogen activator inhibitor-1 (PAI-1) expression was studied in an in vitro shear stress system. Endothelial cells were exposed to either shear stress, the proinflammatory cytokine tumor necrosis factor-? (TNF-a), or a combination of both. High shear stress markedly reduced u-PA expression whereas TNF-a induced u-PA expression. Combining shear stress and inflammatory stimulation reduced the TNF-a mediated u-PA induction, which suggests that shear stress exerts a strong protective effect. The TNF-a induced expression was proposed to be partly mediated by activation of c-jun N-terminal kinase (JNK). The PAI-1 expression was induced both by shear stress and TNF-a, and the effect was potentiated when the two stimuli were combined. In conclusion, these findings illustrate that biomechanical forces regulate a large number of genes in the endothelium and that shear stress and pressure induce distinct expression patterns. Shear stress also has the capacity to influence gene expression in smooth muscle cells in intact vessels and protect against inflammatory stress, which illustrates its potency as a regulator of endothelial cell function.
Source Type:Doctoral Dissertation
Keywords:MEDICINE; shear stress; intraluminal pressure; endothelium; gene expression; DNA microarray; real-time RT-PCR; reference genes; smooth muscle cells; P2 receptors; TNF-alpha; urokinase-type plasminogen activator
Date of Publication:01/01/2007