Department of Women's Health and Division of Reproduction and Endocrinology, King's College London, London, UK.
In Vitro Cell Dev Biol Anim. 2010 Apr;46(3-4):178-85. doi: 10.1007/s11626-010-9276-4. Epub 2010 Feb 23.
Since the derivation of the first human embryonic stem cell (hESC) line in 1998, there has been substantial interest in the potential of these cells for regenerative medicine and cell therapy and in the use of hESCs carrying clinically relevant genetic mutations as models for disease research and therapeutic target identification. There is still a need to improve derivation efficiency and further the understanding of the basic biology of these cells and to develop clinical grade culture systems with the aim of producing cell lines suitable for subsequent manipulation for therapy. The derivation of initial hESC lines at King's College London is discussed here, with focus on derivation methodology. Each of the derivations was distinctive. Although the stage and morphology of each blastocyst were generally similar in each attempt, the behaviour of the colonies was unpredictable; colony morphology and development was different with each attempt. Days 5, 6 and 7 blastocysts were used successfully, and the number of days until appearance of stem-like cells varied from 4 to 14 d. Routine characterisation analyses were performed on three lines, all of which displayed appropriate marker expression and survived cryopreservation-thaw cycles. From the lines discussed, four are at various stages of the deposition process with the UKSCB, one is pending submission and two are unsuitable for banking. Continued open and transparent reporting of results and collaborations will maximise the efficiency of derivation and facilitate the development of standardised protocols for the derivation and early culture of hESC lines.
自 1998 年首次成功分离出人类胚胎干细胞(hESC)以来,人们对这些细胞在再生医学和细胞治疗中的应用以及携带临床相关基因突变的 hESC 作为疾病研究和治疗靶点鉴定模型的潜力产生了浓厚的兴趣。仍需要提高其分离效率,并进一步深入了解这些细胞的基本生物学特性,开发具有临床级别的培养系统,旨在获得适合后续治疗操作的细胞系。本文讨论了伦敦国王学院初始 hESC 系的分离,重点介绍分离方法。每次分离都具有独特性。尽管每个胚胎囊胚的阶段和形态在每次尝试中通常相似,但菌落的行为是不可预测的;每个尝试的菌落形态和发育都不同。成功使用了第 5、6 和 7 天的胚胎囊胚,出现干细胞样细胞的时间从 4 天到 14 天不等。对三条系进行了常规特征分析,所有系均显示出适当的标志物表达,并能在冷冻和解冻循环中存活。在所讨论的系中,有四条系处于英国干细胞委员会的不同存款过程阶段,一条系正在提交中,两条系不适合存款。继续公开透明地报告结果和合作将最大限度地提高分离效率,并促进建立 hESC 系的分离和早期培养的标准化方案。