Son YeonSung, Lee BomNaeRin, Choi Young-Jin, Jeon Seon Ae, Kim Ju-Hyun, Lee Hoo-Keun, Kwon Sang-Mo, Cho Je-Yoel
Department of Biochemistry, BK21 Plus and Research Institute for Veterinary Science, School of Veterinary Medicine, Seoul National University, Seoul, 151-742, Korea.
College of Pharmacy, Gachon University, Incheon 406-840, Republic of Korea.
PLoS One. 2016 Sep 27;11(9):e0163301. doi: 10.1371/journal.pone.0163301. eCollection 2016.
Outgrowth endothelial cells (OECs) are a subpopulation of endothelial progenitor cells (EPCs) that have the capacity for proliferation and the ability to promote angiogenesis. In this study, we identified Nectin-2 as a surface protein of OECs through unbiased quantitative proteomics analysis. Using immunocytochemistry and flow cytometry, we confirmed that Nectin-2 is highly expressed on OECs. Nectin-2 (CD112) expression was limited or lower on mononuclear cells (MNCs) and mature tube-forming endothelial cells (ECs). Blocking Nectin-2 with a neutralizing monoclonal antibody significantly increased the trans-well migration and tube forming capacity of OECs. Similarly, Nectin-2 knockdown resulted in enhanced tube formation, cell migration and proliferation with p-Erk activation. Moreover, Nectin-2 deficiency resulted in compensatory increase of other Nectin family genes including Nectin-3 and Necl-4 which promote VEGFR signaling. These results indicate that Nectin-2 is a surface marker and an important regulator of OECs, with significant implications for the isolation of OECs and blocking Nectin-2 on OECs by an antibody for angiogenic applications.
增殖内皮细胞(OECs)是内皮祖细胞(EPCs)的一个亚群,具有增殖能力和促进血管生成的能力。在本研究中,我们通过无偏倚定量蛋白质组学分析确定Nectin-2为OECs的一种表面蛋白。使用免疫细胞化学和流式细胞术,我们证实Nectin-2在OECs上高度表达。Nectin-2(CD112)在单核细胞(MNCs)和成熟的成管内皮细胞(ECs)上表达受限或较低。用中和单克隆抗体阻断Nectin-2可显著提高OECs的跨膜迁移和管形成能力。同样,Nectin-2基因敲低导致管形成、细胞迁移和增殖增强,并伴有p-Erk激活。此外,Nectin-2缺乏导致包括Nectin-3和Necl-4在内的其他Nectin家族基因的代偿性增加,这些基因促进VEGFR信号传导。这些结果表明,Nectin-2是OECs的一种表面标志物和重要调节因子,对OECs的分离以及通过抗体阻断OECs上的Nectin-2用于血管生成应用具有重要意义。