Institute of Anatomy, Medical Faculty Carl Gustav Carus, Technische Universität Dresden School of Medicine, Fetscherstr 74, 01307, Dresden, Germany.
Angiogenesis. 2024 Aug;27(3):311-331. doi: 10.1007/s10456-024-09911-1. Epub 2024 Apr 2.
Diabetic retinopathy has a high probability of causing visual impairment or blindness throughout the disease progression and is characterized by the growth of new blood vessels in the retina at an advanced, proliferative stage. Microglia are a resident immune population in the central nervous system, known to play a crucial role in regulating retinal angiogenesis in both physiological and pathological conditions, including diabetic retinopathy. Physiologically, they are located close to blood vessels and are essential for forming new blood vessels (neovascularization). In diabetic retinopathy, microglia become widely activated, showing a distinct polarization phenotype that leads to their accumulation around neovascular tufts. These activated microglia induce pathogenic angiogenesis through the secretion of various angiogenic factors and by regulating the status of endothelial cells. Interestingly, some subtypes of microglia simultaneously promote the regression of neovascularization tufts and normal angiogenesis in neovascularization lesions. Modulating the state of microglial activation to ameliorate neovascularization thus appears as a promising potential therapeutic approach for managing diabetic retinopathy.
糖尿病性视网膜病变在疾病进展过程中极有可能导致视力损害或失明,其特征是在晚期增生阶段视网膜新生血管的生长。小胶质细胞是中枢神经系统中的固有免疫群体,已知在生理和病理条件下(包括糖尿病性视网膜病变)在调节视网膜血管生成中发挥关键作用。在生理上,它们靠近血管,对于形成新血管(新生血管形成)至关重要。在糖尿病性视网膜病变中,小胶质细胞广泛激活,表现出明显的极化表型,导致它们在新血管丛周围积聚。这些激活的小胶质细胞通过分泌各种血管生成因子和调节内皮细胞状态来诱导病理性血管生成。有趣的是,小胶质细胞的某些亚型同时促进新血管化丛的消退和新血管化病变中的正常血管生成。调节小胶质细胞激活状态以改善新生血管形成似乎是治疗糖尿病性视网膜病变的一种很有前途的潜在治疗方法。