Department of Anesthesiology, Medical College of Wisconsin, USA.
Department of Medicine, Division of Cardiovascular Medicine, Medical College of Wisconsin, USA.
J Photochem Photobiol B. 2021 Jul;220:112212. doi: 10.1016/j.jphotobiol.2021.112212. Epub 2021 May 12.
Red light (670 nm) promotes ex vivo dilation of blood vessels in a nitric oxide (NO) dependent, but eNOS independent manner by secreting a quasi-stable and transferable vasoactive substance with the characteristics of S-nitrosothiols (RSNO) from the endothelium. In the present work we establish that 670 nm light mediated vasodilation occurs in vivo and is physiologically stable. Light exposure depletes intracellular S-nitroso protein while concomitantly increasing extracellular RNSO, suggesting vesicular pathways are involved. Furthermore, we demonstrate this RSNO vasodilator is embedded in extracellular vesicles (EV). The action of red light on vesicular trafficking appears to increase expression of endosome associated membrane protein CD63 in bovine aortic endothelial cells, enhance endosome localization in the endothelium, and induce exit of RSNO containing EVs from murine facialis arteries. We suggest a mechanism by which the concerted actions of 670 nm light initiate formation of RSNO containing EVs which exit the endothelium and trigger relaxation of smooth muscle cells.
红光(670nm)通过从内皮细胞分泌一种具有 S-亚硝基硫醇(RSNO)特征的准稳定且可传递的血管活性物质,以一氧化氮(NO)依赖但 eNOS 独立的方式促进血管在体扩张。在本工作中,我们确定 670nm 光介导的血管扩张发生在体内并且是生理性稳定的。光照会耗尽细胞内的 S-亚硝基蛋白,同时增加细胞外的 RNSO,这表明涉及囊泡途径。此外,我们证明这种 RSNO 血管扩张剂嵌入在细胞外囊泡(EV)中。红光对囊泡运输的作用似乎会增加牛主动脉内皮细胞中内体相关膜蛋白 CD63 的表达,增强内皮细胞中的内体定位,并诱导含有 RSNO 的 EV 从鼠面动脉中逸出。我们提出了一种机制,即 670nm 光的协同作用启动含有 RSNO 的 EV 的形成,这些 EV 从内皮细胞逸出并触发平滑肌细胞的松弛。