Obert Elisabeth, Strauss Randy, Brandon Carlene, Grek Christina, Ghatnekar Gautam, Gourdie Robert, Rohrer Bärbel
Department of Neuroscience, Medical University of South Carolina, Charleston, SC, 29425, USA.
Center for Heart and Regenerative Medicine, Virginia Tech Carilion Research Institute, Roanoke, VA, 24016, USA.
J Mol Med (Berl). 2017 May;95(5):535-552. doi: 10.1007/s00109-017-1506-8. Epub 2017 Jan 28.
A critical target tissue in age-related macular degeneration (AMD) is the retinal pigment epithelium (RPE), which forms the outer blood-retina barrier (BRB). RPE-barrier dysfunction might result from attenuation/disruption of intercellular tight junctions. Zonula occludens-1 (ZO-1) is a major structural protein of intercellular junctions. A connexin43-based peptide mimetic, αCT1, was developed to competitively block interactions at the PDZ2 domain of ZO-1, thereby inhibiting ligands that selectively bind to this domain. We hypothesized that targeting ZO-1 signaling using αCT1 would maintain BRB integrity and reduce RPE pathophysiology by stabilizing gap- and/or tight-junctions. RPE-cell barrier dysfunction was generated in mice using laser photocoagulation triggering choroidal neovascularization (CNV) or bright light exposure leading to morphological damage. αCT1 was delivered via eye drops. αCT1 treatment reduced CNV development and fluid leakage as determined by optical coherence tomography, and damage was correlated with disruption in cellular integrity of surrounding RPE cells. Light damage significantly disrupted RPE cell morphology as determined by ZO-1 and occludin staining and tiling pattern analysis, which was prevented by αCT1 pre-treatment. In vitro experiments using RPE and MDCK monolayers indicated that αCT1 stabilizes tight junctions, independent of its effects on Cx43. Taken together, stabilization of intercellular junctions by αCT1 was effective in ameliorating RPE dysfunction in models of AMD-like pathology.
The connexin43 mimetic αCT1 accumulates in the mouse retinal pigment epithelium following topical delivery via eye drops. αCT1 eye drops prevented RPE-cell barrier dysfunction in two mouse models. αCT1 stabilizes intercellular tight junctions. Stabilization of cellular junctions via αCT1 may serve as a novel therapeutic approach for both wet and dry age-related macular degeneration.
年龄相关性黄斑变性(AMD)中的一个关键靶组织是视网膜色素上皮(RPE),它形成了外血视网膜屏障(BRB)。RPE屏障功能障碍可能源于细胞间紧密连接的减弱/破坏。闭合蛋白-1(ZO-1)是细胞间连接的一种主要结构蛋白。一种基于连接蛋白43的肽模拟物αCT1被开发出来,以竞争性阻断ZO-1的PDZ2结构域处的相互作用,从而抑制选择性结合该结构域的配体。我们假设使用αCT1靶向ZO-1信号传导将通过稳定缝隙连接和/或紧密连接来维持BRB完整性并减少RPE病理生理学变化。使用激光光凝触发脉络膜新生血管(CNV)或强光照射导致形态学损伤在小鼠中产生RPE细胞屏障功能障碍。αCT1通过滴眼液给药。如通过光学相干断层扫描所确定的,αCT1治疗减少了CNV的发展和液体渗漏,并且损伤与周围RPE细胞的细胞完整性破坏相关。如通过ZO-1和闭合蛋白染色及平铺模式分析所确定的,光损伤显著破坏了RPE细胞形态,而αCT1预处理可预防这种情况。使用RPE和MDCK单层细胞进行的体外实验表明,αCT1稳定紧密连接,与其对Cx43的作用无关。综上所述,αCT1对细胞间连接的稳定在改善AMD样病理模型中的RPE功能障碍方面是有效的。
连接蛋白43模拟物αCT1通过滴眼液局部给药后在小鼠视网膜色素上皮中蓄积。αCT1滴眼液在两种小鼠模型中预防了RPE细胞屏障功能障碍。αCT1稳定细胞间紧密连接。通过αCT1稳定细胞连接可能是湿性和干性年龄相关性黄斑变性的一种新的治疗方法。