Marc and Ruti Bell Vascular Biology and Disease Program, Leon H. Charney Division of Cardiology, Department of Medicine, NewYork University School of Medicine, New York, NY 10016, USA.
Arterioscler Thromb Vasc Biol. 2013 May;33(5):911-9. doi: 10.1161/ATVBAHA.112.301155. Epub 2013 Feb 21.
Emerging evidence suggests that neuronal guidance cues, typically expressed during development, are involved in both physiological and pathological immune responses. We hypothesized that endothelial expression of such guidance cues may regulate leukocyte trafficking into the vascular wall during atherogenesis.
We demonstrate that members of the netrin, semaphorin, and ephrin family of guidance molecules are differentially regulated under conditions that promote or protect from atherosclerosis. Netrin-1 and semaphorin3A are expressed by coronary artery endothelial cells and potently inhibit chemokine-directed migration of human monocytes. Endothelial expression of these negative guidance cues is downregulated by proatherogenic factors, including oscillatory shear stress and proinflammatory cytokines associated with monocyte entry into the vessel wall. Furthermore, we show using intravital microscopy that inhibition of netrin-1 or semaphorin3A using blocking peptides increases leukocyte adhesion to the endothelium. Unlike netrin-1 and semaphorin3A, the guidance cue ephrinB2 is upregulated under proatherosclerotic flow conditions and functions as a chemoattractant, increasing leukocyte migration in the absence of additional chemokines.
The concurrent regulation of negative and positive guidance cues may facilitate leukocyte infiltration of the endothelium through a balance between chemoattraction and chemorepulsion. These data indicate a previously unappreciated role for axonal guidance cues in maintaining the endothelial barrier and regulating leukocyte trafficking during atherogenesis.
新出现的证据表明,神经元导向线索通常在发育过程中表达,它们参与生理和病理免疫反应。我们假设,内皮细胞表达这些导向线索可能会调节白细胞在动脉粥样硬化形成过程中向血管壁的迁移。
我们证明,在促进或预防动脉粥样硬化的条件下,神经导向蛋白、信号素和 Eph 家族的导向分子成员的表达存在差异。轴突导向蛋白-1 和信号素 3A 由冠状动脉内皮细胞表达,并强烈抑制趋化因子指导的人单核细胞迁移。这些负向导向线索的内皮表达受促动脉粥样硬化因子下调,包括与单核细胞进入血管壁相关的振荡剪切应力和促炎细胞因子。此外,我们通过活体显微镜显示,使用阻断肽抑制轴突导向蛋白-1 或信号素 3A 可增加白细胞与内皮的黏附。与轴突导向蛋白-1 和信号素 3A 不同,导向线索 EphrinB2 在促动脉粥样硬化血流条件下上调,并作为趋化因子起作用,在没有其他趋化因子的情况下增加白细胞迁移。
负向和正向导向线索的同时调节可能通过趋化吸引和趋化排斥之间的平衡促进白细胞浸润内皮。这些数据表明,轴突导向线索在维持内皮屏障和调节动脉粥样硬化形成过程中的白细胞迁移方面具有以前未被认识到的作用。