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This Article Free via Open Access: OA OA Full Text Full Text (PDF) OA All Versions of this Article: 2007-0640v1 26/2/465    most recent Alert me when this article is cited Alert me if a correction is posted Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints/Permissions Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Hayes, B. Articles by Torok-Storb, B. Search for Related Content PubMed PubMed Citation Articles by Hayes, B. Articles by Torok-Storb, B.

EMBRYONIC STEM CELLS

Derivation, Characterization, and In Vitro Differentiation of Canine Embryonic Stem Cells

Fred Hutchinson Cancer Research Center, Clinical Research Division, Seattle, Washington, USA

Key Words. Canine • Embryonic stem cells • Tissue-specific stem cells • Hematopoietic cell transplantation • Embryoid bodies

Correspondence: Beverly Torok-Storb, Ph.D., D1-100, Fred Hutchinson Cancer Research Center, Clinical Research Division, 1100 Fairview Avenue North, P.O. Box 19024, Seattle, Washington 98109-1024, USA. Telephone: 206-667-4549; Fax: 206-667-5978; e-mail: btorokst{at}fhcrc.org

Received August 6, 2007; accepted for publication November 22, 2007.
First published online in STEM CELLS EXPRESS   December 6, 2007.



Canine embryonic stem (cES) cell lines were generated to establish a large-animal preclinical model for testing the safety and efficacy of embryonic stem (ES) cell-derived tissue replacement therapy. Putative cES cell lines were initiated from canine blastocysts harvested from natural matings. Times of harvest were estimated as 12–16 days after the presumed surge in circulating levels of luteinizing hormone. Four lines established from blastocysts harvested at days 13–14 postsurge satisfied most of the criteria for embryonic stem cells, whereas lines established after day 14 did not. One line, Fred Hutchinson dog (FHDO)-7, has been maintained through 34 passages and is presented here. FHDO-7 cells are alkaline phosphatase-positive and express both message and protein for the Oct4 transcription factor. They also express message for Nanog and telomerase but do not express message for Cdx2, which is associated with trophectoderm. Furthermore, they express a cluster of pluripotency-associated microRNAs (miRs) (miR-302b, miR-302c, and miR-367) characteristic of human and mouse ES cells. The FHDO-7 cells grow on feeder layers of modified mouse embryonic fibroblasts as flat colonies that resemble ES cells from mink, a close phylogenetic relative of dog. When cultured in nonadherent plates without feeders, the cells form embryoid bodies (EBs). Under various culture conditions, the EBs give rise to ectoderm-derived neuronal cells expressing -enolase and β3-tubulin; mesoderm-derived cells producing collagen IIA1, cartilage, and bone; and endoderm-derived cells expressing -fetoprotein or Clara cell-specific protein.

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

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