Cellartis AB Maclagan House, 1 Würzburg Court, Dundee DD2 1FB, UK.
In Vitro Cell Dev Biol Anim. 2010 Apr;46(3-4):217-30. doi: 10.1007/s11626-010-9289-z. Epub 2010 Feb 23.
This report summarises our efforts in deriving, characterising and banking of 20 different human embryonic stem cell lines. We have derived a large number of human embryonic stem cell lines between 2001 and 2005. One of these cell lines was established under totally xeno-free culture conditions. In addition, several subclones have been established, including a karyoptypical normal clone from a trisomic mother line. A master cell banking system has been utilised in concert with an extensive characterisation programme, ensuring a supply of high quality pluripotent stem cells for further research and development. In this report we also present the first data on a proprietary novel antibody, hES-Cellect, that exhibits high specificity for undifferentiated hES cells. In addition to the traditional manual dissection approach of propagating hES cells, we here also report on the successful approaches of feeder-free cultures as well as single cell cultures based on enzymatic digestion. All culture systems used as reported here have maintained the hES cells in a karyotypical normal and pluripotent state. These systems also have the advantage of being the principal springboards for further scale up of cultures for industrial or clinical applications that would require vastly more cells that can be produced by mechanical means.
本报告总结了我们在衍生、表征和储存 20 种不同的人类胚胎干细胞系方面的努力。我们在 2001 年至 2005 年期间衍生了大量的人类胚胎干细胞系。其中一个细胞系是在完全无动物培养条件下建立的。此外,还建立了几个亚克隆,包括一条来自三体母系的核型正常克隆。我们利用主细胞储存系统和广泛的特征分析计划,确保提供高质量的多能干细胞,用于进一步的研究和开发。在本报告中,我们还介绍了一种新型专有抗体 hES-Cellect 的首批数据,该抗体对未分化的 hES 细胞具有高度特异性。除了传统的手动分离方法来繁殖 hES 细胞外,我们还报告了无饲养层培养以及基于酶消化的单细胞培养的成功方法。这里报告的所有培养系统都使 hES 细胞保持核型正常和多能状态。这些系统还具有优势,可以进一步扩大培养规模,用于工业或临床应用,这些应用需要远远超过机械手段所能产生的更多细胞。