Xu Jinxian, Liu Xinglou, Mo Juan, Marshall Brendan, Perry Libby, Dong Zheng, Zhang Ming
Department of Cellular Biology and Anatomy, Medical College of Georgia, Augusta University, Augusta, GA.
James and Jean Vision Discovery Institute, Medical College of Georgia, Augusta University, Augusta, GA.
Mol Vis. 2018 May 18;24:379-394. eCollection 2018.
The purpose of this study was to determine whether the blood-retina barrier is compromised by choroidal murine cytomegalovirus (MCMV) infection, using electron microscopy.
BALB/c mice were immunosuppressed with methylprednisolone and monoclonal antibodies to CD4 and CD8. At several time points post-MCMV intraperitoneal inoculation, the eyes were removed and analyzed with western blotting and immunoelectron microscopy for the presence of MCMV early antigen (EA) and the host protein RIP3. Posterior eyecups from and mice were cultured and inoculated with MCMV. At days 4, 7, and 11 post-infection, cultures were collected and analyzed with plaque assay, immunohistochemical staining, and real-time PCR (RT-PCR).
MCMV EA was observed in the nuclei of vascular endothelial cells and pericytes in the choriocapillaris. Disruption of Bruch's membrane was observed, especially at sites adjacent to activated platelets, and a few RPE cells containing some enlarged vesicles were found directly beneath disrupted Bruch's membrane. Some virus particles were also observed in the enlarged vesicles of RPE cells. Levels of the RIP3 protein, which was observed mainly in the RPE cells and the basement membrane of the choriocapillaris, were greatly increased following MCMV infection, while depletion of RIP3 resulted in greatly decreased inflammasome formation, as well as expression of downstream inflammation factors.
The results suggest that systemic MCMV spreads to the choroid and replicates in vascular endothelia and pericytes of the choriocapillaris during immunosuppression. Choroidal MCMV infection is associated with in situ inflammation and subsequent disruption of Bruch's membrane and the outer blood-retina barrier.
本研究旨在通过电子显微镜确定脉络膜小鼠巨细胞病毒(MCMV)感染是否会损害血视网膜屏障。
用甲基强的松龙和抗CD4及CD8单克隆抗体对BALB/c小鼠进行免疫抑制。在腹腔接种MCMV后的几个时间点,摘除眼睛,通过蛋白质免疫印迹法和免疫电子显微镜分析MCMV早期抗原(EA)和宿主蛋白RIP3的存在情况。对感染和未感染MCMV的小鼠的眼后杯进行培养并接种MCMV。在感染后第4、7和11天,收集培养物并通过空斑试验、免疫组织化学染色和实时聚合酶链反应(RT-PCR)进行分析。
在脉络膜毛细血管的血管内皮细胞和周细胞的细胞核中观察到MCMV EA。观察到布鲁赫膜的破坏,尤其是在与活化血小板相邻的部位,并且在破坏的布鲁赫膜正下方发现了一些含有一些扩大囊泡的视网膜色素上皮(RPE)细胞。在RPE细胞扩大的囊泡中也观察到一些病毒颗粒。主要在RPE细胞和脉络膜毛细血管基底膜中观察到的RIP3蛋白水平在MCMV感染后大幅增加;而RIP3的缺失导致炎性小体形成大幅减少,以及下游炎症因子的表达减少。
结果表明,在免疫抑制期间,全身性MCMV扩散到脉络膜并在脉络膜毛细血管的血管内皮细胞和周细胞中复制。脉络膜MCMV感染与原位炎症以及随后的布鲁赫膜和外血视网膜屏障破坏有关。