Bakker Erik N T P, Matlung Hanke L, Bonta Peter, de Vries Carlie J, van Rooijen Nico, Vanbavel Ed
Department of Medical Physics, Academic Medical Center, Amsterdam, the Netherlands.
Cardiovasc Res. 2008 May 1;78(2):341-8. doi: 10.1093/cvr/cvn050. Epub 2008 Feb 24.
Altered blood flow affects vascular tone, attracts inflammatory cells, and leads to microvascular remodelling. We tested the hypothesis that inflammation facilitates the remodelling response, but that vascular tone determines its direction (inward or outward).
Mouse mesenteric resistance arteries were ligated to create either increased blood flow or low blood flow in vivo. In vivo microscopy was used to determine changes in vascular tone. Structural remodelling was studied after 2 days, with or without macrophage depletion. In order to characterize the inflammatory response, immunostaining, confocal microscopy, and real-time PCR were used. To address the role of vascular tone in remodelling, arteries were treated with the vasodilator amlodipine during organ culture. Vessels exposed to high blood flow dilated, whereas low flow induced constriction. After 1 day, inflammatory markers showed a complex but remarkably similar increase in expression during high flow and low flow. Both high-flow and low-flow vessels showed an increase in the number of adventitial macrophages. Depletion of macrophages eliminated flow-induced remodelling. Manipulation of vascular tone reversed inward remodelling in response to low blood flow.
Altered blood flow triggers an inflammatory response that facilitates remodelling. Vascular tone is a crucial determinant of the direction of the remodelling response.
血流改变会影响血管张力,吸引炎症细胞,并导致微血管重塑。我们检验了以下假设:炎症促进重塑反应,但血管张力决定其方向(向内或向外)。
结扎小鼠肠系膜阻力动脉,在体内造成血流增加或血流减少。利用体内显微镜检查来确定血管张力的变化。在有或没有巨噬细胞清除的情况下,于2天后研究结构重塑。为了表征炎症反应,采用了免疫染色、共聚焦显微镜检查和实时聚合酶链反应。为了探讨血管张力在重塑中的作用,在器官培养期间用血管扩张剂氨氯地平处理动脉。暴露于高血流的血管扩张,而低血流则诱导血管收缩。1天后,炎症标志物在高血流和低血流期间显示出复杂但明显相似的表达增加。高血流和低血流血管的外膜巨噬细胞数量均增加。巨噬细胞清除消除了血流诱导的重塑。血管张力的调节逆转了对低血流的向内重塑。
血流改变引发促进重塑的炎症反应。血管张力是重塑反应方向的关键决定因素。