Wang Yuwen, Yang Mei, Wang Xuan, Zou Huan, Chen Xiaofan, Yuan Rongdi
Department of Ophthalmology, Xinqiao Hospital, Army Medical University, Xinqiao Road, Shapingba District, Chongqing, 400037, China.
Department of Ophthalmology, Daping Hospital, Army Medical University, Chongqing, 400042, China.
Mol Biotechnol. 2025 Jun;67(6):2467-2480. doi: 10.1007/s12033-024-01210-w. Epub 2024 Jun 12.
Retinal microangiopathies, such as neovascularization and preretinal and vitreous hemorrhages, are the primary pathological features of diabetic retinopathy (DR). These conditions can worsen visual impairment and may result in blindness. Furthermore, multiple metabolic pathways are associated with microangiopathy in DR. However, the specific underlying pathological mechanisms remain unclear. Several studies have demonstrated the important role of G protein-coupled receptor 124 (Gpr124) in cerebral vascular endothelial cells, but its effect on the retinal endothelium has not been elucidated. In this study, we found that Gpr124 is expressed in both pathological retinal fibrous vascular membranes of DR patients and retinal blood vessels of mice, with elevated protein expression specifically observed in the retinas of DR model mice. Furthermore, Gpr124 expression was elevated after high-glucose treatment of human retinal microvascular endothelial cells (HRMECs). Inhibition of Gpr124 expression affected the high glucose-induced proliferation, migration, and tube-forming ability of HRMECs. We concluded that Gpr124 expression was upregulated in DR and promoted HRMECs angiogenesis in a high-glucose environment. This finding may help to elucidate the pathogenesis of DR and provide a critical research basis for identifying effective treatments.
视网膜微血管病变,如新生血管形成、视网膜前和玻璃体出血,是糖尿病视网膜病变(DR)的主要病理特征。这些情况会加重视力损害,并可能导致失明。此外,多种代谢途径与DR中的微血管病变有关。然而,具体的潜在病理机制仍不清楚。多项研究已证明G蛋白偶联受体124(Gpr124)在脑血管内皮细胞中的重要作用,但其对视网膜内皮的影响尚未阐明。在本研究中,我们发现Gpr124在DR患者的病理性视网膜纤维血管膜和小鼠视网膜血管中均有表达,在DR模型小鼠的视网膜中特异性观察到蛋白表达升高。此外,人视网膜微血管内皮细胞(HRMECs)经高糖处理后,Gpr124表达升高。抑制Gpr124表达影响高糖诱导的HRMECs增殖、迁移和管形成能力。我们得出结论,DR中Gpr124表达上调,并在高糖环境中促进HRMECs血管生成。这一发现可能有助于阐明DR的发病机制,并为确定有效治疗方法提供关键的研究基础。