From the Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder (C.Z., M.B.L., V.J., Z.C., H.J.J.).
Department of Ophthalmology, University of Colorado School of Medicine, Aurora (M.G.P., J.M.P.).
Arterioscler Thromb Vasc Biol. 2018 Nov;38(11):2691-2705. doi: 10.1161/ATVBAHA.118.311689.
Objective- Blood-CNS (central nervous system) barrier defects are implicated in retinopathies, neurodegenerative diseases, stroke, and epilepsy, yet, the pathological mechanisms downstream of barrier defects remain incompletely understood. Blood-retina barrier (BRB) formation and retinal angiogenesis require β-catenin signaling induced by the ligand norrin (NDP [Norrie disease protein]), the receptor FZD4 (frizzled 4), coreceptor LRP5 (low-density lipoprotein receptor-like protein 5), and the tetraspanin TSPAN12 (tetraspanin 12). Impaired NDP/FZD4 signaling causes familial exudative vitreoretinopathy, which may lead to blindness. This study seeked to define cell type-specific functions of TSPAN12 in the retina. Approach and Results- A loxP-flanked Tspan12 allele was generated and recombined in endothelial cells using a tamoxifen-inducible Cdh5-CreERT2 driver. Resulting phenotypes were documented using confocal microscopy. RNA-Seq, histopathologic analysis, and electroretinogram were performed on retinas of aged mice. We show that TSPAN12 functions in endothelial cells to promote vascular morphogenesis and BRB formation in developing mice and BRB maintenance in adult mice. Early loss of TSPAN12 in endothelial cells causes lack of intraretinal capillaries and increased VE-cadherin (CDH5 [cadherin5 aka VE-cadherin]) expression, consistent with premature vascular quiescence. Late loss of TSPAN12 strongly impairs BRB maintenance without affecting vascular morphogenesis, pericyte coverage, or perfusion. Long-term BRB defects are associated with immunoglobulin extravasation, complement deposition, cystoid edema, and impaired b-wave in electroretinograms. RNA-sequencing reveals transcriptional responses to the perturbation of the BRB, including genes involved in vascular basement membrane alterations in diabetic retinopathy. Conclusions- This study establishes mice with late endothelial cell-specific loss of Tspan12 as a model to study pathological consequences of BRB impairment in an otherwise intact vasculature.
目的-血脑屏障(CNS)缺陷与视网膜病变、神经退行性疾病、中风和癫痫有关,但屏障缺陷下游的病理机制仍不完全清楚。血视网膜屏障(BRB)的形成和视网膜血管生成需要β-连环蛋白信号,该信号由配体诺里(NDP[诺里病蛋白])、受体 FZD4(卷曲蛋白 4)、辅助受体 LRP5(低密度脂蛋白受体样蛋白 5)和四跨膜蛋白 TSPAN12(四跨膜蛋白 12)诱导。NDP/FZD4 信号受损会导致家族性渗出性玻璃体视网膜病变,可能导致失明。本研究旨在确定 TSPAN12 在视网膜中的细胞类型特异性功能。方法和结果-生成了一个loxP 侧翼 Tspan12 等位基因,并使用他莫昔芬诱导的 Cdh5-CreERT2 驱动在血管内皮细胞中进行重组。使用共聚焦显微镜记录所得表型。对老年小鼠的视网膜进行 RNA-Seq、组织病理学分析和视网膜电图检查。我们表明,TSPAN12 在血管内皮细胞中发挥作用,可促进发育中小鼠的血管形态发生和 BRB 形成,并维持成年小鼠的 BRB。内皮细胞中 TSPAN12 的早期缺失导致视网膜内毛细血管缺失和 VE-钙粘蛋白(CDH5[钙粘蛋白 5,又名 VE-钙粘蛋白])表达增加,这与血管过早静止一致。内皮细胞中 TSPAN12 的晚期缺失强烈损害 BRB 的维持,而不影响血管形态发生、周细胞覆盖或灌注。长期的 BRB 缺陷与免疫球蛋白渗出、补体沉积、囊样水肿和视网膜电图 b 波受损有关。RNA 测序揭示了对 BRB 扰动的转录反应,包括参与糖尿病视网膜病变中血管基底膜改变的基因。结论-本研究建立了内皮细胞特异性晚期缺失 Tspan12 的小鼠模型,用于研究在完整血管中 BRB 损伤的病理后果。