Laminar Shear Stress Regulates Endothelial Kinin B1 Receptor Expression and Function Potential Implication in Atherogenesis

作者:Duchene Johan; Cayla Cecile; Vessillier Sandrine; Scotland Ramona; Yamashiro Kazuo; Lecomte Florence; Syed Irfan; Vo Phuong; Marrelli Alessandra; Pitzalis Costantino; Cipollone Francesco; Schanstra Joost; Bascands Jean Loup; Hobbs Adrian J; Perretti Mauro; Ahluwalia Amrita*
来源:Arteriosclerosis, Thrombosis, and Vascular Biology, 2009, 29(11): 1757-1763.
DOI:10.1161/ATVBAHA.109.191775

摘要

Objective-The proinflammatory phenotype induced by low laminar shear stress (LSS) is implicated in atherogenesis. The kinin B1 receptor (B1R), known to be induced by inflammatory stimuli, exerts many proinflammatory effects including vasodilatation and leukocyte recruitment. We investigated whether low LSS is a stimulus for endothelial B1R expression and function. Methods and Results-Human and mouse atherosclerotic plaques expressed high level of B1R mRNA and protein. In addition, B1R expression was upregulated in the aortic arch (low LSS region) of ApoE(-/-) mice fed a high-fat diet compared to vascular regions of high LSS and animals fed normal chow. Of interest, a greater expression of B1R was noticed in endothelial cells from regions of low LSS in aortic arch of ApoE(-/-) mice. B1R was also upregulated in human umbilical vein endothelial cells (HUVECs) exposed to low LSS (0 to 2 dyn/cm(2)) compared to physiological LSS (6 to 10 dyn/cm(2)): an effect similarly evident in murine vascular tissue perfused ex vivo. Functionally, B1R activation increased prostaglandin and CXCL5 expression in cells exposed to low, but not physiological, LSS. IL-1 beta and ox-LDL induced B1R expression and function in HUVECs, a response substantially enhanced under low LSS conditions and inhibited by blockade of NF kappa B activation. Conclusion-Herein, we show that LSS is a major determinant of functional B1R expression in endothelium. Furthermore, whereas physiological high LSS is a powerful repressor of this inflammatory receptor, low LSS at sites of atheroma is associated with substantial upregulation, identifying this receptor as a potential therapeutic target. (Arterioscler Thromb Vasc Biol. 2009; 29: 1757-1763.)