Horie Shintaro, Robbie Scott J, Liu Jian, Wu Wei-Kang, Ali Robin R, Bainbridge James W, Nicholson Lindsay B, Mochizuki Manabu, Dick Andrew D, Copland David A
1] Academic Unit of Ophthalmology, School of Clinical Sciences, University of Bristol, Bristol, UK [2] Department of Ophthalmology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan [3].
Sci Rep. 2013 Oct 30;3:3072. doi: 10.1038/srep03072.
Macrophages are rapidly conditioned by cognate and soluble signals to acquire phenotypes that deliver specific functions during inflammation, wound healing and angiogenesis. Whether inhibitory CD200R signaling regulates pro-angiogenic macrophage phenotypes with the potential to suppress ocular neovascularization is unknown. CD200R-deficient bone marrow derived macrophages (BMMΦ) were used to demonstrate that macrophages lacking this inhibitory receptor exhibit enhanced levels of Vegfa, Arg-1 and Il-1β when stimulated with PGE2 or RPE-conditioned (PGE2-enriched) media. Endothelial tube formation in HUVECs was increased when co-cultured with PGE2-conditioned CD200R(-/-) BMMΦ, and laser-induced choroidal neovascularization was enhanced in CD200R-deficient mice. In corroboration, signaling through CD200R results in the down-regulation of BMMΦ angiogenic and pro-inflammatory phenotypes. Translational potential of this pathway was investigated in the laser-induced model of choroidal neovascularization. Local delivery of a CD200R agonist mAb to target myeloid infiltrate alters macrophage phenotype and inhibits pro-angiogenic gene expression, which suppresses pathological angiogenesis and CNV development.
巨噬细胞可被同源信号和可溶性信号迅速调节,以获得在炎症、伤口愈合和血管生成过程中发挥特定功能的表型。抑制性CD200R信号是否调节具有抑制眼新生血管形成潜力的促血管生成巨噬细胞表型尚不清楚。利用CD200R缺陷的骨髓来源巨噬细胞(BMMΦ)证明,缺乏这种抑制性受体的巨噬细胞在用PGE2或视网膜色素上皮细胞条件培养基(富含PGE2)刺激时,Vegfa、Arg-1和Il-1β水平会升高。当与PGE2条件培养基处理的CD200R(-/-)BMMΦ共培养时,人脐静脉内皮细胞(HUVEC)中的内皮管形成增加,并且在CD200R缺陷小鼠中激光诱导的脉络膜新生血管形成增强。与此一致的是,通过CD200R发出的信号导致BMMΦ血管生成和促炎表型的下调。在激光诱导的脉络膜新生血管形成模型中研究了该途径的转化潜力。向靶向髓样浸润部位局部递送CD200R激动剂单克隆抗体可改变巨噬细胞表型并抑制促血管生成基因表达,从而抑制病理性血管生成和脉络膜新生血管的发展。