A Survey of Parameters Involved in the Establishment of New Lines of Human Embryonic Stem Cells

被引:14
作者
Fraga, Ana Maria [1 ]
Souza de Araujo, Erica Sara [1 ]
Stabellini, Raquel [1 ]
Vergani, Naja [1 ]
Pereira, Lygia V. [1 ]
机构
[1] Univ Sao Paulo, Lab Nacl Celulas Tronco Embrionarias, Inst Nacl Ciencia & Tecnol Celulas Tronco & Terap, Dept Genet & Biol Evolutiva,Inst Biociencias, BR-05508090 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Human embryonic stem cells; Cell line derivation; Pluripotency; Human embryo; Cell therapy; POOR-QUALITY EMBRYOS; HUMAN BLASTOCYSTS; DERIVATION; CULTURE; DIFFERENTIATION; INACTIVATION; POPULATION; DIVERSITY;
D O I
10.1007/s12015-011-9250-x
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Since the derivation of the first human embryonic stem cell (hESC) lines by Thomson and coworkers in 1998, more than 1,200 different hESC lines have been established worldwide. Nevertheless, there is still a recognized interest in the establishment of new lines of hESC, particularly from HLA types and ethnic groups currently underrepresented among the available lines. The methodology of hESC derivation has evolved significantly since 1998, when human LIF (hLIF) was used for maintenance of pluripotency. However, there are a number of different strategies for the several steps involved in establishing a new line of hESC. Here we make a survey of the most relevant parameters used between 1998 and 2010 for the derivation of the 375 hESC lines deposited in two international stem cell registries, and able to form teratomas in immunocompromised mice. Although we identify some trends in the methodology for establishing hESC lines, our data reveal a much greater heterogeneity of strategies than what is used for derivation of murine ESC lines, indicating that optimum conditions have not been consolidated yet, and thus, hESC establishment is still an evolving field of research.
引用
收藏
页码:775 / 781
页数:7
相关论文
共 41 条
[1]   Clonally derived human embryonic stem cell lines maintain pluripotency and proliferative potential for prolonged periods of culture [J].
Amit, M ;
Carpenter, MK ;
Inokuma, MS ;
Chiu, CP ;
Harris, CP ;
Waknitz, MA ;
Itskovitz-Eldor, J ;
Thomson, JA .
DEVELOPMENTAL BIOLOGY, 2000, 227 (02) :271-278
[2]   Human ES cell lines-introduction [J].
Andrews, Peter W. ;
Benvenisty, Nissim ;
Knowles, Barbara B. ;
McKay, Ronald D. G. ;
Oh, Steve K. W. ;
Pera, Martin F. ;
Rossant, Janet ;
Stacey, Glyn N. .
IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL, 2010, 46 (3-4) :167-168
[3]   International stem cell registries [J].
Borstlap, Joeri ;
Luong, Mai X. ;
Rooke, Heather M. ;
Aran, B. ;
Damaschun, A. ;
Elstner, A. ;
Smith, Kelly P. ;
Stein, Gary S. ;
Veiga, Anna .
IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL, 2010, 46 (3-4) :242-246
[4]   Characterization of six new human embryonic stem cell lines (HSF7, -8, -9, -10, -12, and -13) derived under minimal-animal component conditions [J].
Chavez, Shawn L. ;
Meneses, Juanito J. ;
Nguyen, Ha Nam ;
Kim, Seung K. ;
Pera, Renee A. Reijo .
STEM CELLS AND DEVELOPMENT, 2008, 17 (03) :535-546
[5]   Optimal Timing of Inner Cell Mass Isolation Increases the Efficiency of Human Embryonic Stem Cell Derivation and Allows Generation of Sibling Cell Lines [J].
Chen, Alice E. ;
Egli, Dieter ;
Niakan, Kathy ;
Deng, Jie ;
Akutsu, Hidenori ;
Yamaki, Mariko ;
Cowan, Chad ;
Fitz-Gerald, Claire ;
Zhang, Kun ;
Melton, Douglas A. ;
Eggan, Kevin .
CELL STEM CELL, 2009, 4 (02) :103-106
[6]   Human embryonic stem cell lines generated without embryo destruction [J].
Chung, Young ;
Klimanskaya, Irina ;
Becker, Sandy ;
Li, Tong ;
Maserati, Marc ;
Lu, Shi-Jiang ;
Zdravkovic, Tamara ;
Ilic, Dusko ;
Genbacev, Olga ;
Fisher, Susan ;
Krtolica, Ana ;
Lanza, Robert .
CELL STEM CELL, 2008, 2 (02) :113-117
[7]  
Cowan CA, 2004, NEW ENGL J MED, V350, P1353, DOI 10.1056/NEJMsr040330
[8]   LIF/STAT3 signaling fails to maintain self-renewal of human embryonic stem cells [J].
Dahéron, L ;
Opitz, SL ;
Zaehres, H ;
Lensch, WM ;
Andrews, PW ;
Itskovitz-Eldor, J ;
Daley, GQ .
STEM CELLS, 2004, 22 (05) :770-778
[9]   High-resolution analysis of the subtelomeric regions of human embryonic stem cells [J].
Darnfors, C ;
Flodin, A ;
Andersson, K ;
Caisander, G ;
Lindqvist, J ;
Hyllner, J ;
Wahlström, J ;
Sartipy, P .
STEM CELLS, 2005, 23 (04) :483-488
[10]   The immunogenicity of human embryonic stem-derived cells [J].
Drukker, M ;
Benvenisty, N .
TRENDS IN BIOTECHNOLOGY, 2004, 22 (03) :136-141