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EMBRYONIC STEM CELLS

Heterozygous Embryonic Stem Cell Lines Derived from Nonhuman Primate Parthenotes

^aOregon National Primate Research Center,
^dOregon Stem Cell Center, and
^eDepartment of Obstetrics and Gynecology, Oregon Health & Science University, Beaverton, Oregon, USA;
^bWhitehead Institute for Biomedical Research, Cambridge, Massachusetts, USA;
^cVeterinary Genetics Laboratory, University of California, Davis, California, USA

Key Words. Embryonic stem cells • Parthenogenetic • Meiotic recombination • Imprinting • Histocompatible

Correspondence: Correspondence: Shoukhrat Mitalipov, Ph.D., 505 NW 185th Avenue, Beaverton, Oregon 97006, USA. Telephone: 503-614-3709; Fax: 503-533-2494; e-mail: mitalipo{at}ohsu.edu

Received on October 15, 2007; accepted for publication on December 27, 2007.

First published online in STEM CELLS EXPRESS  January 10, 2008.


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.

Disclosure of potential conflicts of interest is found at the end of this article.

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