Tu Yuanyuan, Luo Yalu, Zhao Qingliang, Zeng Yanfeng, Leng Kai, Zhu Manhui
Department of Ophthalmology, Lixiang Eye Hospital of Soochow University, Suzhou, Jiangsu, China.
Suzhou Medical College, Soochow University, Suzhou, China.
Heliyon. 2024 May 7;10(10):e30840. doi: 10.1016/j.heliyon.2024.e30840. eCollection 2024 May 30.
Ocular neovascularization is the leading cause of blindness in clinical settings. Pathological angiogenesis of the eye can be divided into corneal neovascularization (CoNV), retinal neovascularization (RNV, including diabetic retinopathy and retinopathy of prematurity), and choroidal neovascularization (CNV) based on the anatomical location of abnormal neovascularization. Although anti-Vascular endothelial growth factor (VEGF) agents have wide-ranging clinical applications and are an effective treatment for neovascular eye disease, many deficiencies in this treatment strategy remain. Recently, emerging evidence has demonstrated that macrophages are vital during the process of physiological and pathological angiogenesis. Monocyte-macrophage lineage is diverse and plastic, they can shift between different activation modes and have different functions. Due to the obvious regulatory effect of macrophages on inflammation and angiogenesis, macrophages have been increasingly studied in the field of ophthalmology. Here, we detail how macrophage activated and the role of different subtypes of macrophages in the pathogenesis of ocular neovascularization. The complexity of macrophages has recently taken center stage owing to their subset diversity and tightly regulated molecular and metabolic phenotypes. In this review, we reveal the functional and phenotypic characterization of macrophage subsets associated with ocular neovascularization, more in-depth research is needed to explore the specific mechanisms by which macrophages regulate angiogenesis as well as macrophage polarization. Targeted regulation of macrophage differentiation based on their phenotype and function could be an effective approach to treat and manage ocular neovascularization in the future.
眼部新生血管形成是临床环境中导致失明的主要原因。根据异常新生血管形成的解剖位置,眼部病理性血管生成可分为角膜新生血管形成(CoNV)、视网膜新生血管形成(RNV,包括糖尿病视网膜病变和早产儿视网膜病变)和脉络膜新生血管形成(CNV)。尽管抗血管内皮生长因子(VEGF)药物在临床上有广泛应用,且是治疗新生血管性眼病的有效方法,但该治疗策略仍存在许多不足之处。最近,新出现的证据表明巨噬细胞在生理性和病理性血管生成过程中至关重要。单核细胞-巨噬细胞谱系多样且具有可塑性,它们可以在不同激活模式之间转换并具有不同功能。由于巨噬细胞对炎症和血管生成具有明显的调节作用,巨噬细胞在眼科领域受到越来越多的研究。在此,我们详细阐述巨噬细胞如何被激活以及不同亚型巨噬细胞在眼部新生血管形成发病机制中的作用。由于巨噬细胞亚群的多样性以及其分子和代谢表型受到严格调控,巨噬细胞的复杂性最近成为了研究的焦点。在本综述中,我们揭示了与眼部新生血管形成相关的巨噬细胞亚群的功能和表型特征,需要更深入的研究来探索巨噬细胞调节血管生成以及巨噬细胞极化的具体机制。基于巨噬细胞的表型和功能进行靶向调控可能是未来治疗和管理眼部新生血管形成的有效方法。