Pluripotency of embryonic stem cells

被引:52
作者
Yamanaka, Satoshi [1 ]
Li, Jinliang [1 ]
Kania, Gabriela [2 ]
Elliott, Steve [3 ]
Wersto, Robert P. [1 ]
Van Eyk, Jennifer [3 ]
Wobus, Anna M. [2 ]
Boheler, Kenneth R. [1 ]
机构
[1] NIA, Gerontol Res Ctr, Cardiovasc Sci Lab, Baltimore, MD 21224 USA
[2] Leibniz Inst IPK Gatersleben, In Vitro Differentiat Grp, D-06466 Gatersleben, Germany
[3] Johns Hopkins Univ, Dept Med, Baltimore, MD USA
关键词
embryonic stem cells; pluripotency; differentiation; development;
D O I
10.1007/s00441-007-0520-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Embryonic stem (ES) cells derived from pre-implantation embryos have the potential to differentiate into any cell type derived from the three germ layers of ectoderm (epidermal tissues and nerves), mesoderm (muscle, bone, blood), and endoderm (liver, pancreas, gastrointestinal tract, lungs), including fetal and adult cells. Alone, these cells do not develop into a viable fetus or adult animal because they do not retain the potential to contribute to extraembryonic tissue, and in vitro, they lack spatial and temporal signaling cues essential to normal in vivo development. The basis of pluripotentiality resides in conserved regulatory networks composed of numerous transcription factors and multiple signaling cascades. Together, these regulatory networks maintain ES cells in a pluripotent and undifferentiated form; however, alterations in the stoichiometry of these signals promote differentiation. By taking advantage of this differentiation capacity in vitro, ES cells have clearly been shown to possess the potential to generate multipotent stem and progenitor cells capable of differentiating into a limited number of cell fates. These latter types of cells may prove to be therapeutically viable, but perhaps more importantly, the studies of these cells have led to a greater understanding of mammalian development.
引用
收藏
页码:5 / 22
页数:18
相关论文
共 134 条
[1]   Synergistic activation of the fibroblast growth factor 4 enhancer by Sox2 and Oct-3 depends on protein-protein interactions facilitated by a specific spatial arrangement of factor binding sites [J].
Ambrosetti, DC ;
Basilico, C ;
Dailey, L .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (11) :6321-6329
[2]   Feeder layer- and serum-free culture of human embryonic stem cells [J].
Amit, M ;
Shariki, C ;
Margulets, V ;
Itskovitz-Eldor, J .
BIOLOGY OF REPRODUCTION, 2004, 70 (03) :837-845
[3]  
Androutsellis-Theotokis A, 2006, NATURE, V442, P823, DOI 10.1038/nature04940
[4]   The appearance of truncated cyclin A2 correlates with differentiation of mouse embryonic stem cells [J].
Anger, M ;
Bryja, V ;
Jirmanova, L ;
Hampl, A ;
Carrington, M ;
Motlik, J ;
Dvorak, P ;
Kubelka, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 302 (04) :825-830
[5]   Functional gene screening in embryonic stem cells implicates Wnt antagonism in neural differentiation [J].
Aubert, J ;
Dunstan, H ;
Chambers, I ;
Smith, A .
NATURE BIOTECHNOLOGY, 2002, 20 (12) :1240-1245
[6]   Multipotent cell lineages in early mouse development depend on SOX2 function [J].
Avilion, AA ;
Nicolis, SK ;
Pevny, LH ;
Perez, L ;
Vivian, N ;
Lovell-Badge, R .
GENES & DEVELOPMENT, 2003, 17 (01) :126-140
[7]   Differentiation of embryonal stem cells into keratinocytes: Comparison of wild-type and beta(1) integrin-deficient cells [J].
Bagutti, C ;
Wobus, AM ;
Fassler, R ;
Watt, FM .
DEVELOPMENTAL BIOLOGY, 1996, 179 (01) :184-196
[8]   Generation of skeletal muscle from transplanted embryonic stem cells in dystrophic mice [J].
Bhagavati, S ;
Xu, WM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 333 (02) :644-649
[9]   Embryonic stem cells differentiate into insulin-producing cells without selection of nestin-expressing cells [J].
Blyszczuk, P ;
Asbrand, C ;
Rozzo, A ;
Kania, G ;
St-Onge, L ;
Rupnik, M ;
Wobus, AM .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY, 2004, 48 (10) :1095-1104
[10]   Expression of Pax4 in embryonic stem cells promotes differentiation of nestin-positive progenitor and insulin-producing cells [J].
Blyszczuk, P ;
Czyz, J ;
Kania, G ;
Wagner, M ;
Roll, U ;
St-Onge, L ;
Wobus, AM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (03) :998-1003