The derivation of clinical-grade human embryonic stem cell lines

被引:38
作者
Skottman, Heli
Dilber, M. Sirac
Hovatta, Outi [1 ]
机构
[1] Univ Tampere, Inst Regenerat Med, FI-33520 Tampere, Finland
[2] Tampere Univ Hosp, FI-33520 Tampere, Finland
[3] Karolinska Univ Hosp Huddinge, Karolinska Inst, Dept Med, SE-14186 Stockholm, Sweden
[4] Karolinska Univ Hosp Huddinge, Karolinska Inst, Dept Clin Sci Intervent & Technol, SE-14186 Stockholm, Sweden
关键词
human embryonic stem cells; derivation; culture; good manufacturing practice;
D O I
10.1016/j.febslet.2006.03.083
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The pluripotent nature of human embryonic stem cells (hESC) has attracted great interest in using them as a source of cells or tissue in cell therapy. However, in order to be used in regenerative medicine, the pluripotent hESC lines should be established and propagated according to good manufacturing practice quality requirements. The cultures should be animal substance free in order to exclude the risk of infections and immunogenity. They should also be genetically and epigenetically normal. The detailed molecular mechanisms of their pluripotency are still not defined. Using human feeder cells, a medium containing only human proteins, the mechanical isolation of the inner cell mass and mechanical passaging of hESC, is a safe option until a functional defined medium containing physiological concentrations of regulatory factors is available. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2875 / 2878
页数:4
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