Progress with nonhuman primate embryonic stem cells

被引:44
作者
Wolf, DP
Kuo, HC
Pau, KYF
Lester, L
机构
[1] Oregon Hlth & Sci Univ, Oregon Natl Primate Res Ctr, Beaverton, OR 97006 USA
[2] Oregon Hlth & Sci Univ, Div Reprod Sci, Beaverton, OR 97006 USA
[3] Oregon Hlth & Sci Univ, Dept Med, Portland, OR 97201 USA
关键词
assisted reproductive technology; developmental biology; diabetes; differentiation; early development; embryo; monkey; primate; regenerative medicine; stem cells;
D O I
10.1095/biolreprod.104.029413
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Embryonic stem cells hold potential in the fields of regenerative medicine, developmental biology, tissue regeneration, disease pathogenicity, and drug discovery. Embryonic stem (ES) cell lines are now available in primates, including man, rhesus, and cynomologous monkeys. Monkey ES cells serve as invaluable clinically relevant models for studies that can't be conducted in humans because of practical or ethical limitations, or in rodents because of differences in physiology and anatomy. Here, we review the current status of nonhuman primate research with ES cells, beginning with a description of their isolation, characterization, and availability. Substantial limitations still plague the use of primate ES cells, such as their required growth on feeder layers, poor cloning efficiency, and restricted availability. The ability to produce homogenous populations of both undifferentiated as well as differentiated phenotypes is an important challenge, and genetic approaches to achieving these objectives are discussed. Finally, safety, efficiency, and feasibility issues relating to the transplantation of ES-derived cells are considered.
引用
收藏
页码:1766 / 1771
页数:6
相关论文
共 43 条
[1]   Engraftment and tumor formation after allogeneic in utero transplantation of primate embryonic stem cells [J].
Asano, T ;
Ageyama, N ;
Takeuchi, K ;
Momoeda, M ;
Kitano, Y ;
Sasaki, K ;
Ueda, Y ;
Suzuki, Y ;
Kondo, Y ;
Torii, R ;
Hasegawa, M ;
Ookawara, S ;
Harii, K ;
Terao, K ;
Ozawa, K ;
Hanazono, Y .
TRANSPLANTATION, 2003, 76 (07) :1061-1067
[2]  
AZAKA TP, 2003, NAT BIOTECHNOL, V21, P319
[3]   Setting standards for human embryonic stem cells [J].
Brivanlou, AH ;
Gage, FH ;
Jaenisch, R ;
Jessell, T ;
Melton, D ;
Rossant, J .
SCIENCE, 2003, 300 (5621) :913-+
[4]   Signalling, cell cycle and pluripotency in embryonic stem cells [J].
Burdon, T ;
Smith, A ;
Savatier, P .
TRENDS IN CELL BIOLOGY, 2002, 12 (09) :432-438
[5]   Portrait of a stem cell [J].
Burns, CE ;
Zon, LI .
DEVELOPMENTAL CELL, 2002, 3 (05) :612-613
[6]   Parthenogenetic stem cells in nonhuman primates [J].
Cibelli, Jose B. ;
Grant, Kathleen A. ;
Chapman, Karen B. ;
Cunniff, Kerrianne ;
Worst, Travis ;
Green, Heather L. ;
Walker, Stephen J. ;
Gutin, Philip H. ;
Vilner, Lucy ;
Tabar, Viviane ;
Dominko, Tanja ;
Kane, Jeff ;
Wettstein, Peter J. ;
Lanza, Robert P. ;
Studer, Lorenz ;
Vrana, Kent E. ;
West, Michael D. .
Science, 2002, 295 (5556)
[7]   Safety issues in cell-based intervention trials [J].
Dawson, L ;
Bateman-House, AS ;
Agnew, DM ;
Bok, H ;
Brock, DW ;
Chakravarti, A ;
Greene, M ;
King, PA ;
O'Brien, SJ ;
Sachs, DH ;
Schill, KE ;
Siegel, A ;
Solter, D ;
Suter, SM ;
Verfaillie, CM ;
Walters, LB ;
Gearhart, JD ;
Faden, RR .
FERTILITY AND STERILITY, 2003, 80 (05) :1077-1085
[8]   Surface antigens of human embryonic stem cells: changes upon differentiation in culture [J].
Draper, JS ;
Pigott, C ;
Thomson, JA ;
Andrews, PW .
JOURNAL OF ANATOMY, 2002, 200 (03) :249-258
[9]   A molecular view on pluripotent stem cells [J].
Eiges, R ;
Benvenisty, N .
FEBS LETTERS, 2002, 529 (01) :135-141
[10]  
Fortunel NO, 2003, SCIENCE, V302, P393