Heterozygous embryonic stem cell lines derived from nonhuman primate parthenotes

被引:46
作者
Dighe, Vikas [1 ]
Clepper, Lisa [1 ]
Pedersen, Darlene [1 ]
Byrne, James [1 ]
Ferguson, Betsy [1 ]
Gokhale, Sumita [4 ]
Penedo, M. Cecilia T. [5 ]
Wolf, Don [1 ]
Mitalipov, Shoukhrat [1 ,2 ,3 ]
机构
[1] Oregon Hlth & Sci Univ, Oregon Natl Primate Res Ctr, Beaverton, OR USA
[2] Oregon Hlth & Sci Univ, Oregon Stem Cell Ctr, Beaverton, OR USA
[3] Oregon Hlth & Sci Univ, Dept Obstet & Gynecol, Beaverton, OR USA
[4] MIT, Whitehead Inst Biomed Res, Cambridge, MA USA
[5] Univ Calif Davis, Vet Gen Lab, Davis, CA 95616 USA
关键词
embryonic stem cells; parthenogenetic; meiotic recombination; imprinting; histocompatible;
D O I
10.1634/stemcells.2007-0869
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Monoparental parthenotes represent a potential source of histocompatible stem cells that should be isogenic with the oocyte donor and therefore suitable for use in cell or tissue replacement therapy. We generated five rhesus monkey parthenogenetic embryonic stem cell (PESC) lines with stable, diploid female karyotypes that were morphologically indistinguishable from biparental controls, expressed key pluripotent markers, and generated cell derivatives representative of all three germ layers following in vivo and in vitro differentiation. Interestingly, high levels of heterozygosity were observed at the majority of loci that were polymorphic in the oocyte donors. Some PESC lines were also heterozygous in the major histocompatibility complex region, carrying haplotypes identical to those of the egg donor females. Expression analysis revealed transcripts from some imprinted genes that are normally expressed from only the paternal allele. These results indicate that limitations accompanying the potential use of PESC-derived phenotypes in regenerative medicine, including aberrant genomic imprinting and high levels of homozygosity, are cell line-dependent and not always present. PESC lines were derived in high enough yields to be practicable, and their derivatives are suitable for autologous transplantation into oocyte donors or could be used to establish a bank of histocompatible cell lines for a broad spectrum of patients.
引用
收藏
页码:756 / 766
页数:11
相关论文
共 37 条
[1]  
ALLEN ND, 1994, DEVELOPMENT, V120, P1473
[2]   ROLE OF PATERNAL AND MATERNAL GENOMES IN MOUSE DEVELOPMENT [J].
BARTON, SC ;
SURANI, MAH ;
NORRIS, ML .
NATURE, 1984, 311 (5984) :374-376
[3]   Producing primate embryonic stem cells by somatic cell nuclear transfer [J].
Byrne, J. A. ;
Pedersen, D. A. ;
Clepper, L. L. ;
Nelson, M. ;
Sanger, W. G. ;
Gokhale, S. ;
Wolf, D. P. ;
Mitalipov, S. M. .
NATURE, 2007, 450 (7169) :497-U3
[4]   Transcriptional profiling of rhesus monkey embryonic stem cells [J].
Byrne, James A. ;
Mitalipov, Shoukhrat M. ;
Clepper, Lisa ;
Wolf, Don P. .
BIOLOGY OF REPRODUCTION, 2006, 75 (06) :908-915
[5]   Selection of transplant donors based on MHC microsatellite data (vol 51, pg 106, 1996) [J].
Carrington, M ;
Wade, J .
HUMAN IMMUNOLOGY, 1996, 51 (02) :106-109
[6]  
CAVENEE WK, 1989, CLIN CHEM, V35, pB48
[7]   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)
[8]  
Cui HM, 2002, CANCER RES, V62, P6442
[9]  
Dean W, 1998, DEVELOPMENT, V125, P2273
[10]  
DomingoRoura X, 1997, AM J PRIMATOL, V43, P357, DOI 10.1002/(SICI)1098-2345(1997)43:4<357::AID-AJP7>3.0.CO