Donnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
Department of Molecular Genetics, University of Toronto, Toronto, M5S 1A8, Canada.
Sci Rep. 2019 Jan 29;9(1):842. doi: 10.1038/s41598-018-37462-1.
Cell surface antigen discovery is of great interest for biomedical research both for isolation of rare cell populations and therapeutic targeting. We developed a rapid, cost-effective, fully in vitro technology which facilities the simultaneous target discovery and human antibody generation on the surface of virtually any cell population of interest. We apply our technique to human colorectal cancer-initiating cells (CICs) and identify hundreds of unique human antibodies. We characterized the top three antibody candidates targeting these CICs and identify their protein targets as integrin α7 (ITGA7), HLA-A1 and integrin β6 (ITGB6). We demonstrate that these antibodies can be used to isolate self-renewing colorectal CICs, and that the integrin α7 antibody can prospectively identify glioblastoma brain tumor initiating cells as well as human muscle stem cells. We also demonstrate that genetic ablation of integrin β6 impedes colorectal CIC function. The methodology can be readily applied to other cell populations including stem cells, cancer, or immune cells to facilitate the rapid identification of novel targets and simultaneous generation of potent and specific antibodies with therapeutic potential.
细胞表面抗原的发现对于生物医学研究具有重要意义,既可以用于分离稀有细胞群体,也可以用于治疗性靶向。我们开发了一种快速、经济有效的、完全在体外的技术,该技术可以在实际上任何有兴趣的细胞群体的表面同时进行目标发现和人类抗体的产生。我们将我们的技术应用于人类结直肠肿瘤起始细胞(CICs),并鉴定了数百种独特的人类抗体。我们对针对这些 CICs 的三种顶级抗体候选物进行了表征,并鉴定了它们的蛋白靶标为整合素α7(ITGA7)、HLA-A1 和整合素β6(ITGB6)。我们证明这些抗体可用于分离自我更新的结直肠 CICs,并且整合素α7 抗体可以前瞻性地鉴定神经胶质瘤脑肿瘤起始细胞以及人类肌肉干细胞。我们还证明,整合素β6 的基因缺失会阻碍结直肠 CIC 的功能。该方法可以很容易地应用于其他细胞群体,包括干细胞、癌症或免疫细胞,以促进对新型靶标的快速识别以及同时产生具有治疗潜力的有效和特异性抗体。