Tonade Deoye, Liu Haitao, Kern Timothy S
Department of Pharmacology Case Western Reserve University, Cleveland, Ohio, United States.
Department of Medicine, Case Western Reserve University, Cleveland, Ohio, United States.
Invest Ophthalmol Vis Sci. 2016 Aug 1;57(10):4264-71. doi: 10.1167/iovs.16-19859.
Recent studies suggest that photoreceptor cells regulate local inflammation in the retina in diabetes. The purpose of this study was to determine if photoreceptor cells themselves produce inflammatory proteins in diabetes and if soluble factors released by photoreceptors in elevated glucose induce inflammatory changes in nearby cells.
Laser capture microdissection was used to isolate the outer retina (photoreceptors) from the inner retina in nondiabetic and diabetic mice. Diabetes-induced changes in the expression of inflammatory targets were assessed by reverse transcription polymerase chain reaction and immunohistochemistry. Cell culture experiments were carried out to determine if photoreceptors in vitro and ex vivo release soluble mediators that can stimulate nearby cells. Photoreceptor contribution to leukocyte-mediated endothelial cell death was tested using coculture models.
Messenger ribonucleic acid and protein expression levels for inflammatory proteins intercellular adhesion molecule 1 (ICAM1), inducible nitric oxide synthase (iNOS), and cyclooxygenase 2 (COX2) were increased in photoreceptors cells in diabetes. In vitro and ex vivo studies show that photoreceptor cells in elevated glucose release mediators that can induce tumor necrosis factor-α in leukocytes and endothelial cells, but not in glia. The soluble mediators released by photoreceptor cells in elevated glucose are regulated by transforming growth factor β-activated kinase 1 and nicotinamide adenine dinucleotide phosphate oxidase (NADPH oxidase) signaling. In contrast to enhanced leukocyte-mediated killing of endothelial cells by leukocytes from wild-type diabetic mice, leukocytes from diabetic mice lacking photoreceptor cells (opsin-/-) did not kill endothelial cells.
These data indicate that photoreceptor cells are a source of inflammatory proteins in diabetes, and their release of soluble mediators can contribute to the death of retinal capillaries in diabetes.
近期研究表明,光感受器细胞可调节糖尿病视网膜中的局部炎症。本研究旨在确定光感受器细胞自身在糖尿病中是否会产生炎症蛋白,以及在高糖环境下光感受器释放的可溶性因子是否会诱导附近细胞发生炎症变化。
采用激光捕获显微切割技术,从非糖尿病和糖尿病小鼠的视网膜内层分离出外层视网膜(光感受器)。通过逆转录聚合酶链反应和免疫组织化学评估糖尿病诱导的炎症靶点表达变化。进行细胞培养实验,以确定体外和离体的光感受器是否释放可刺激附近细胞的可溶性介质。使用共培养模型测试光感受器对白细胞介导的内皮细胞死亡的影响。
糖尿病小鼠的光感受器细胞中,炎症蛋白细胞间黏附分子1(ICAM1)、诱导型一氧化氮合酶(iNOS)和环氧化酶2(COX2)的信使核糖核酸和蛋白质表达水平升高。体外和离体研究表明,高糖环境下的光感受器细胞释放的介质可诱导白细胞和内皮细胞而非神经胶质细胞产生肿瘤坏死因子-α。高糖环境下光感受器细胞释放的可溶性介质受转化生长因子β激活激酶1和烟酰胺腺嘌呤二核苷酸磷酸氧化酶(NADPH氧化酶)信号通路调控。与野生型糖尿病小鼠的白细胞增强对内皮细胞的杀伤作用相反,缺乏光感受器细胞(视蛋白基因敲除小鼠)的糖尿病小鼠的白细胞并未杀伤内皮细胞。
这些数据表明,光感受器细胞是糖尿病中炎症蛋白的来源,其释放的可溶性介质可能导致糖尿病视网膜毛细血管的死亡。