Boston University School of Medicine, Boston, MA, USA.
Boston University School of Medicine, Boston, MA, USA.
Prog Retin Eye Res. 2021 May;82:100903. doi: 10.1016/j.preteyeres.2020.100903. Epub 2020 Sep 18.
Vascular basement membrane (BM) thickening has been hailed over half a century as the most prominent histological lesion in diabetic microangiopathy, and represents an early ultrastructural change in diabetic retinopathy (DR). Although vascular complications of DR have been clinically well established, specific cellular and molecular mechanisms underlying dysfunction of small vessels are not well understood. In DR, small vessels develop insidiously as BM thickening occurs. Studies examining high resolution imaging data have established BM thickening as one of the foremost structural abnormalities of retinal capillaries. This fundamental structural change develops, at least in part, from excess accumulation of BM components. Although BM thickening is closely associated with the development of DR, its contributory role in the pathogenesis of DR is coming to light recently. DR develops over several years before clinical manifestations appear, and it is during this clinically silent period that hyperglycemia induces excess synthesis of BM components, contributes to vascular BM thickening, and promotes structural and functional lesions including cell death and vascular leakage in the diabetic retina. Studies using animal models show promising results in preventing BM thickening with subsequent beneficial effects. Several gene regulatory approaches are being developed to prevent excess synthesis of vascular BM components in an effort to reduce BM thickening. This review highlights current understanding of capillary BM thickening development, role of BM thickening in retinal vascular lesions, and strategies for preventing vascular BM thickening as a potential therapeutic strategy in alleviating characteristic lesions associated with DR.
血管基底膜 (BM) 增厚在半个多世纪以来一直被誉为糖尿病微血管病变中最突出的组织学病变,是糖尿病性视网膜病变 (DR) 的早期超微结构改变。尽管 DR 的血管并发症在临床上已经得到很好的证实,但小血管功能障碍的具体细胞和分子机制尚不清楚。在 DR 中,随着 BM 增厚,小血管逐渐发生病变。对高分辨率成像数据的研究已经确立了 BM 增厚是视网膜毛细血管最重要的结构异常之一。这种基本的结构变化至少部分是由于 BM 成分的过度积累而发生的。尽管 BM 增厚与 DR 的发生密切相关,但它在 DR 发病机制中的作用最近才被揭示。DR 在出现临床症状之前需要数年时间才能发展,而正是在这段临床无症状期间,高血糖会导致 BM 成分过度合成,导致血管 BM 增厚,并促进结构和功能损伤,包括糖尿病视网膜中的细胞死亡和血管渗漏。使用动物模型的研究显示,预防 BM 增厚具有很大的前景,并能带来后续的有益效果。目前正在开发几种基因调控方法来防止血管 BM 成分的过度合成,以减少 BM 增厚。本文综述了目前对毛细血管 BM 增厚发展的认识、BM 增厚在视网膜血管病变中的作用,以及预防血管 BM 增厚作为缓解与 DR 相关特征性病变的潜在治疗策略。