Horrocks Grace M, Lauder Lyndsey, Stewart Rebecca, Przyborski Stefan
School of Biological and Biomedical Sciences, University of Durham, South Road, Durham, DH1 3LE, UK.
Biochem Biophys Res Commun. 2003 May 2;304(2):411-6. doi: 10.1016/s0006-291x(03)00611-9.
Embryonal carcinoma (EC) stem cells derived from germ cell tumours are valuable tools for the study of embryogenesis and closely resemble embryonic stem cells. When human TERA2.cl.SP12 EC cells are exposed to retinoic acid and grown as adherent monolayers, approximately 10-15% of cells commit toward becoming neurons whilst the remainder of cells produce non-neuronal cell types. Using established protocols it is possible to isolate and purify neurons from these cultures but such a process takes several weeks and the numbers of neurons produced are relatively low. In this study, we describe the development of novel procedures to enhance neuronal productivity with dramatically increased efficiency, which will be of value for research purposes and drug discovery programmes.
源自生殖细胞肿瘤的胚胎癌(EC)干细胞是研究胚胎发生的宝贵工具,与胚胎干细胞极为相似。当人类TERA2.cl.SP12 EC细胞暴露于视黄酸并作为贴壁单层细胞生长时,约10 - 15%的细胞会向神经元方向分化,而其余细胞则产生非神经元细胞类型。利用既定方案,从这些培养物中分离和纯化神经元是可行的,但这个过程需要数周时间,且产生的神经元数量相对较少。在本研究中,我们描述了开发新方法以显著提高神经元生成效率的过程,这对于研究目的和药物发现计划具有重要价值。