Yang Yu, Liu Fang, Tang Miao, Yuan Miner, Hu Andina, Zhan Zongyi, Li Zijing, Li Jiaqing, Ding Xiaoyan, Lu Lin
State Key Laboratory of Ophthalmology, Retina Division, Zhongshan Ophthalmic Center, Sun Yat-sen University, 510060, Guangzhou, Guangdong, China.
Sci Rep. 2016 Aug 4;6:30933. doi: 10.1038/srep30933.
Macrophages play an important role in the development of age-related macular degeneration (AMD). In this study, the spatial and temporal changes and the polarization of macrophages in murine laser-induced choroidal neovascularization (CNV) were investigated, and the polarized M1 and M2 biomarkers in the aqueous humors of neovascular AMD (nAMD) patients were studied. Macrophages, the main infiltrating inflammatory cells in CNV lesions, were evidenced by a significant increase in F4/80 mRNA expression and by the infiltration of F4/80+ cells in the lesions and the vicinity of laser-induced CNV. The mRNA expressions of M1-related markers were dramatically upregulated in the early stage, while the M2-related markers were slightly upregulated in the middle stage and sustained until the late stage. The results of immunostaining showed a similar early-but-transient M1 pattern and a delayed-but-sustained M2 pattern in laser-induced CNV. In addition, a higher M2/M1 ratio was found in both the murine models (Arg-1/iNOS and CCL22/CXCL10) and the aqueous humors of nAMD patients (CCL22/CXCL10) than in the controls. Our results suggested that the dynamic patterns of M1 and M2 were different in both the experimental and clinical CNV. The M2 macrophages were predominant and may play a more important role in the development of CNV.
巨噬细胞在年龄相关性黄斑变性(AMD)的发展中起重要作用。在本研究中,研究了小鼠激光诱导脉络膜新生血管(CNV)中巨噬细胞的时空变化及极化情况,并研究了新生血管性AMD(nAMD)患者房水中极化的M1和M2生物标志物。巨噬细胞是CNV病变中主要浸润的炎性细胞,F4/80 mRNA表达显著增加以及F4/80+细胞在激光诱导的CNV病变及其附近浸润证明了这一点。M1相关标志物的mRNA表达在早期显著上调,而M2相关标志物在中期略有上调并持续至晚期。免疫染色结果显示,激光诱导的CNV中存在类似的早期但短暂的M1模式和延迟但持续的M2模式。此外,在小鼠模型(Arg-1/iNOS和CCL22/CXCL10)和nAMD患者房水(CCL22/CXCL10)中发现的M2/M1比值均高于对照组。我们的结果表明,在实验性和临床CNV中,M1和M2的动态模式不同。M2巨噬细胞占主导地位,可能在CNV的发展中起更重要的作用。