Ocular Angiogenesis Group, Departments of Ophthalmology and Cell Biology and Histology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Department of Molecular Ophthalmology, Lions Eye Institute, Nedlands, Western Australia, Australia.
Exp Eye Res. 2014 May;122:123-31. doi: 10.1016/j.exer.2014.03.005. Epub 2014 Apr 3.
The molecular mechanisms of vascular leakage in diabetic macular edema and proliferative retinopathy are poorly understood, mainly due to the lack of reliable in vivo models. The Akimba (Ins2(Akita)VEGF(+/-)) mouse model combines retinal neovascularization with hyperglycemia, and in contrast to other models, displays the majority of signs of advanced clinical diabetic retinopathy (DR). To study the molecular mechanism that underlies the breakdown of the blood-retinal barrier (BRB) in diabetic macular edema and proliferative diabetic retinopathy, we investigated the retinal vasculature of Akimba and its parental mice Kimba (trVEGF029) and Akita (Ins2(Akita)). Quantitative PCR, immunohistochemistry and fluorescein angiography were used to characterize the retinal vasculature with special reference to the inner BRB. Correlations between the degree of fluorescein leakage and retinal gene expression were tested by calculating the Spearman's correlation coefficient. Fluorescein leakage demonstrating BRB loss was observed in Kimba and Akimba, but not in Akita or wild type mice. In Kimba and Akimba mice fluorescein leakage was associated with focal angiogenesis and correlated significantly with Plvap gene expression. PLVAP is an endothelial cell-specific protein that is absent in intact blood-retinal barrier, but its expression significantly increases in pathological conditions such as DR. Furthermore, in Akimba mice BRB disruption was linked to decreased expression of endothelial junction proteins, pericyte dropout and vessel loss. Despite fluorescein leakage, no alteration in BRB protein levels or pericyte coverage was detected in retinas of Kimba mice. In summary, our data not only demonstrate that hyperglycemia sensitizes retinal vasculature to the effects of VEGF, leading to more severe microvascular changes, but also confirm an important role of PLVAP in the regulation of BRB permeability.
糖尿病性黄斑水肿和增生性视网膜病变中血管渗漏的分子机制尚不清楚,主要是因为缺乏可靠的体内模型。Akimba(Ins2(Akita)VEGF(+/-))小鼠模型结合了视网膜新生血管形成和高血糖,与其他模型相比,该模型显示了大多数晚期临床糖尿病性视网膜病变(DR)的迹象。为了研究糖尿病性黄斑水肿和增生性糖尿病性视网膜病变中血视网膜屏障(BRB)破裂的分子机制,我们研究了 Akimba 及其亲本小鼠 Kimba(trVEGF029)和 Akita(Ins2(Akita))的视网膜血管。定量 PCR、免疫组织化学和荧光血管造影用于描述视网膜血管,特别参考了内 BRB。通过计算 Spearman 相关系数来测试荧光素渗漏与视网膜基因表达之间的相关性。在 Kimba 和 Akimba 小鼠中观察到 BRB 丢失的荧光素渗漏,但在 Akita 或野生型小鼠中未观察到。在 Kimba 和 Akimba 小鼠中,荧光素渗漏与局灶性血管生成相关,并与 Plvap 基因表达显著相关。PLVAP 是一种内皮细胞特异性蛋白,在完整的血视网膜屏障中不存在,但在 DR 等病理条件下其表达显著增加。此外,在 Akimba 小鼠中,BRB 破坏与内皮细胞连接蛋白表达减少、周细胞脱落和血管丢失有关。尽管存在荧光素渗漏,但 Kimba 小鼠的视网膜中未检测到 BRB 蛋白水平或周细胞覆盖的改变。总之,我们的数据不仅表明高血糖使视网膜血管对 VEGF 的作用敏感,导致更严重的微血管变化,而且还证实了 PLVAP 在调节 BRB 通透性方面的重要作用。