Basic fibroblast growth factor supports undifferentiated human embryonic stem cell growth without conditioned medium

被引:287
作者
Xu, CH [1 ]
Rosler, E [1 ]
Jiang, JJ [1 ]
Lebkowski, JS [1 ]
Gold, JD [1 ]
O'Sullivan, C [1 ]
Delavan-Boorsma, K [1 ]
Mok, M [1 ]
Bronstein, A [1 ]
Carpenter, MK [1 ]
机构
[1] Geron Corp, Menlo Pk, CA 94025 USA
关键词
human embryonic stem cells; growth factors; telomerase; stem cell markers; differentiation;
D O I
10.1634/stemcells.2004-0211
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Previous studies have shown that prolonged propagation of undifferentiated human embryonic stem cells (hESCs) requires conditioned medium from mouse embryonic feeders (MEF-CM) as well as matrix components. Because hESCs express growth factor receptors, including those for basic fibroblast growth factor (bFGF), stem cell factor (SCF), and fetal liver tyrosine kinase-3 ligand (Flt3L), we evaluated these and other growth factors for their ability to maintain undifferentiated hESCs in the absence of conditioned medium. We found cultures maintained in bFGF alone or in combination with other factors showed characteristics similar to MEF-CM control cultures, including morphology, surface marker and transcription factor expression, telomerase activity, differentiation, and karyotypic stability. In contrast, cells in media containing Flt-3L, thrombopoietin, and SCF, individually or in combination, showed almost complete differentiation after 6 weeks in culture. These data demonstrate that hESCs can be maintained in nonconditioned medium using growth factors.
引用
收藏
页码:315 / 323
页数:9
相关论文
共 55 条
[21]   Human embryonic stem cells can differentiate into myocytes with structural and functional properties of cardiomyocytes [J].
Kehat, I ;
Kenyagin-Karsenti, D ;
Snir, M ;
Segev, H ;
Amit, M ;
Gepstein, A ;
Livne, E ;
Binah, O ;
Itskovitz-Eldor, J ;
Gepstein, L .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (03) :407-414
[22]   SPECIFIC ASSOCIATION OF HUMAN TELOMERASE ACTIVITY WITH IMMORTAL CELLS AND CANCER [J].
KIM, NW ;
PIATYSZEK, MA ;
PROWSE, KR ;
HARLEY, CB ;
WEST, MD ;
HO, PLC ;
COVIELLO, GM ;
WRIGHT, WE ;
WEINRICH, SL ;
SHAY, JW .
SCIENCE, 1994, 266 (5193) :2011-2015
[23]  
Lebkowski JS, 2001, CANCER J, V7, pS83
[24]   Endothelial cells derived from human embryonic stem cells [J].
Levenberg, S ;
Golub, JS ;
Amit, M ;
Itskovitz-Eldor, J ;
Langer, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (07) :4391-4396
[25]  
LUSKEY BD, 1992, BLOOD, V80, P396
[26]   TARGETED DISRUPTION OF THE FLK2/FLT3 GENE LEADS TO DEFICIENCIES IN PRIMITIVE HEMATOPOIETIC PROGENITORS [J].
MACKAREHTSCHIAN, K ;
HARDIN, JD ;
MOORE, KA ;
BOAST, S ;
GOFF, SP ;
LEMISCHKA, IR .
IMMUNITY, 1995, 3 (01) :147-161
[27]   EFFECT OF STEEL FACTOR AND LEUKEMIA INHIBITORY FACTOR ON MURINE PRIMORDIAL GERM-CELLS IN CULTURE [J].
MATSUI, Y ;
TOKSOZ, D ;
NISHIKAWA, S ;
NISHIKAWA, SI ;
WILLIAMS, D ;
ZSEBO, K ;
HOGAN, BLM .
NATURE, 1991, 353 (6346) :750-752
[28]   DERIVATION OF PLURIPOTENTIAL EMBRYONIC STEM-CELLS FROM MURINE PRIMORDIAL GERM-CELLS IN CULTURE [J].
MATSUI, Y ;
ZSEBO, K ;
HOGAN, BLM .
CELL, 1992, 70 (05) :841-847
[29]   FGF MODULATES THE PDGF-DRIVEN PATHWAY OF OLIGODENDROCYTE DEVELOPMENT [J].
MCKINNON, RD ;
MATSUI, T ;
DUBOISDALCQ, M ;
AARONSON, SA .
NEURON, 1990, 5 (05) :603-614
[30]   Cardiomyocyte differentiation of mouse and human embryonic stem cells [J].
Mummery, C ;
Ward, D ;
van den Brink, CE ;
Bird, SD ;
Doevendans, PA ;
Opthof, T ;
de la Riviere, AB ;
Tertoolen, L ;
van der Heyden, M ;
Pera, M .
JOURNAL OF ANATOMY, 2002, 200 (03) :233-242