脉络膜新生血管
CCR2型
生物
巨噬细胞
基因剔除小鼠
黄斑变性
肿瘤坏死因子α
免疫学
新生血管
单核细胞
四氯化碳
癌症研究
病理
受体
炎症
趋化因子
血管生成
趋化因子受体
医学
视网膜
眼科
遗传学
体外
生物化学
作者
Chikako Tsutsumi,Koh‐Hei Sonoda,Kensuke Egashira,Hong Qiao,Toshio Hisatomi,Shintaro Nakao,Minako Ishibashi,Israel Charo,Taiji Sakamoto,Toshinori Murata,Tatsuro Ishibashi
摘要
Abstract Choroidal neovascularization (CNV) is directly related to visual loss in some eye diseases, such as age-related macular degeneration. Although several human histological studies have suggested the participation of macrophages in CNV formation, the precise mechanisms are still not fully understood. In this study, we elucidated the role of ocular-infiltrating macrophages in experimental CNV using CCR2 knockout (KO) mice, wild-type mice, and C57BL/6 (B6) mice. CCR2 is the receptor of monocyte chemoattractant protein-1, and the number of infiltrating macrophage and the area of CNV were significantly reduced in CCR2 KO mice. Enriched ocular-infiltrating macrophages from B6 mice actually showed angiogenic ability in a dorsal air sac assay. Moreover, their expression of class II, CD40, B7-1 and B7-2 molecules, and the mRNA for potential angiogenic factors, such as vascular endothelial growth factor, basic fibroblast growth factor, and tumor necrosis factor α, was also observed. Collectively, we conclude that ocular-infiltrating macrophages play an important role in CNV generation.
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