Embryonic stem cells from parthenotes

被引:31
作者
Cibelli, Jose B. [1 ]
Cunniff, Kerrianne
Vrana, Kent E.
机构
[1] Michigan State Univ, Dept Anim Sci, E Lansing, MI 48824 USA
[2] Michigan State Univ, Dept Physiol, E Lansing, MI 48824 USA
来源
EMBRYONIC STEM CELLS | 2006年 / 418卷
关键词
D O I
10.1016/S0076-6879(06)18008-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
While human embryonic stem cells (hESCs) hold tremendous therapeutic potential, they also create societal and ethical dilemmas. Adult and placental stem cells represent two alternatives to the hESC, but may have technical limitations. An additional alternative is the stem cell derived from parthenogenesis. Parthenogenesis is a reproductive mechanism that is common in lower organisms and produces a live birth from an oocyte activated in the absence of sperm. However, parthenogenetic embryos will develop to the blastocyst stage and so can serve as a source of embryonic stem cells. Parthenogenetic ESCs (pESCs) have been shown to have the properties of self-renewal and the capacity to generate cell derivatives from the three germ layers, confirmed by contributions to chimeric animals and/or teratoma formation when injected into SCID mice. Therefore, this mechanism for generating stem cells has the ethical advantage of not involving the destruction of viable embryos. Moreover, the cells do not involve the union of male and female and so genetic material will be derived exclusively from the female oocyte donor (with the attendant potential immunological advantages). This chapter describes the biology underlying parthenogenesis, as well as provides detailed technical considerations for the production of pESCs.
引用
收藏
页码:117 / 135
页数:19
相关论文
共 46 条
[1]  
ALLEN ND, 1994, DEVELOPMENT, V120, P1473
[2]   Fusion with activated mouse oocytes modulates the transcriptional activity of introduced somatic cell nuclei [J].
Borsuk, E ;
Szollosi, MS ;
Besombes, D ;
Debey, P .
EXPERIMENTAL CELL RESEARCH, 1996, 225 (01) :93-101
[3]   Meiotic and mitotic Ca2+ oscillations affect cell composition in resulting blastocysts [J].
BosMikich, A ;
Whittingham, DG ;
Jones, KT .
DEVELOPMENTAL BIOLOGY, 1997, 182 (01) :172-179
[4]   Cloned rabbits produced by nuclear transfer from adult somatic cells [J].
Chesné, P ;
Adenot, PG ;
Viglietta, C ;
Baratte, M ;
Boulanger, L ;
Renard, JP .
NATURE BIOTECHNOLOGY, 2002, 20 (04) :366-369
[5]  
Cibelli J.B., 2001, J REGEN MED, V2, P25, DOI [10.1089/152489001753262168, DOI 10.1089/152489001753262168]
[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]   PARTHENOGENETIC ACTIVATION OF MOUSE OOCYTES INVITRO WITH ETHANOL AND BENZYL ALCOHOL [J].
CUTHBERTSON, KSR .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 1983, 226 (02) :311-314
[8]   Effect of 6-dimethylaminopurine on electrically activated in vitro matured porcine oocytes [J].
Grupen, CG ;
Mau, JC ;
McIlfatrick, SM ;
Maddocks, S ;
Nottle, MB .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 2002, 62 (03) :387-396
[9]   Cell cycle-coupled [Ca2+]i oscillations in mouse zygotes and function of the inositol 1,4,5-trisphosphate receptor-1 [J].
Jellerette, T ;
Kurokawa, M ;
Lee, B ;
Malcuit, C ;
Yoon, SY ;
Smyth, J ;
Vermassen, E ;
De Smedt, H ;
Parys, JB ;
Fissore, RA .
DEVELOPMENTAL BIOLOGY, 2004, 274 (01) :94-109
[10]  
KAUFMAN MH, 1983, J EMBRYOL EXP MORPH, V73, P249