Yu Dao-Yi, Su Er-Ning, Mehnert Andrew, Yu Paula K, Cringle Stephen J, Morgan William H, McAllister Ian L
Lions Eye Institute, Perth, Western Australia, Australia; Centre for Ophthalmology and Visual Science, The University of Western Australia, Perth, Western Australia, Australia.
Lions Eye Institute, Perth, Western Australia, Australia; Centre for Ophthalmology and Visual Science, The University of Western Australia, Perth, Western Australia, Australia.
Exp Eye Res. 2023 Mar;228:109386. doi: 10.1016/j.exer.2023.109386. Epub 2023 Jan 16.
We have previously reported that porcine retinal veins can be contracted by vasoactive factors such as endothelin-1, but it is still unknown which cells play the major role in such contraction responses. This study seeks to confirm whether retinal vein endothelial cells play a significant role in the endothelin-1 induced contraction of porcine retinal veins. This is a novel study which provides confirmation of the endothelial cells' ability to contract retinal veins using a live vessel preparation. Retinal veins were isolated from porcine retina and cannulated for perfusion. The vessels were exposed to extraluminal delivery of endothelin-1 (10 M) and change in vessel diameter recorded automatically every 2 s. A phase contrast objective lens was also used to capture images of the endothelial cell morphometries. The length, width, area, and perimeter were assessed. In addition, vein histology and immuno-labeling for contractile proteins was performed. With 10 M endothelin-1 contractions to 63.6% of baseline were seen. The polygonal shape of the endothelial cells under normal tone became spindle-like after contraction. The area, width, perimeter and length were significantly reduced by 54.8%, 48.1%, 28.5% and 10.5% respectively. Three contractile proteins, myosin, calponin and alpha-SMA were found in retinal vein endothelial cells. Retinal vein endothelial cells contain contractile proteins and can be contracted by endothelin-1 administration. Such contractile capability may be important in regulating retinal perfusion but could also be a factor in the pathogenesis of retinal vascular diseases such as retinal vein occlusion. As far as we are aware, this is the first study on living isolated veins to confirm that endothelial cells contribute to the endothelin-1 induced contraction.
我们之前曾报道,猪视网膜静脉可被内皮素 -1 等血管活性因子收缩,但仍不清楚哪种细胞在此类收缩反应中起主要作用。本研究旨在证实视网膜静脉内皮细胞在猪视网膜静脉内皮素 -1 诱导的收缩中是否发挥重要作用。这是一项新颖的研究,通过活体血管制备证实了内皮细胞收缩视网膜静脉的能力。从猪视网膜分离出视网膜静脉并插管进行灌注。将血管暴露于管腔外给予的内皮素 -1(10 μM),每 2 秒自动记录血管直径的变化。还使用相差物镜拍摄内皮细胞形态测量的图像。评估其长度、宽度、面积和周长。此外,进行了静脉组织学检查和收缩蛋白的免疫标记。给予 10 μM 内皮素 -1 后,可见收缩至基线的 63.6%。正常张力下内皮细胞的多边形形状在收缩后变为纺锤形。面积、宽度、周长和长度分别显著减少了 54.8%、48.1%、28.5%和 10.5%。在视网膜静脉内皮细胞中发现了三种收缩蛋白,肌球蛋白、钙调蛋白和α -平滑肌肌动蛋白。视网膜静脉内皮细胞含有收缩蛋白,可通过给予内皮素 -1 而收缩。这种收缩能力可能在调节视网膜灌注中很重要,但也可能是视网膜静脉阻塞等视网膜血管疾病发病机制中的一个因素。据我们所知,这是第一项关于活体分离静脉的研究,证实了内皮细胞促成内皮素 -1 诱导的收缩。