Journal of Leukocyte Biology
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Originally published online as doi:10.1189/jlb.0106015 on July 24, 2006

Published online before print July 24, 2006
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(Journal of Leukocyte Biology. 2006;80:816-826.)
© 2006 by Society for Leukocyte Biology

Characterization, isolation, and differentiation of murine skin cells expressing hematopoietic stem cell markers

Simone Meindl*, Uwe Schmidt{dagger}, Christine Vaculik* and Adelheid Elbe-Bürger*,1

* Department of Dermatology, Division of Immunology, Allergy and Infectious Diseases, and
{dagger} Institute of Immunology, Vienna Competence Center, Medical University of Vienna, Vienna, Austria

1 Correspondence: Department of Dermatology, Division of Immunology, Allergy and Infectious Diseases, Vienna Competence Center, Medical University of Vienna, Lazarettgasse 19, Vienna 1090 , Austria. E-mail: adelheid.elbe-buerger{at}meduniwien.ac.at

As the phenotype of adult dermal stem cells is still elusive, and the hematopoietic stem cell is one of the best-characterized stem cells in the body, we tested dermal cell suspensions, sections, and wholemounts in newborn and adult mice for hematopoietic stem cell marker expression. Phenotypic analysis revealed that a small population of CD45+ cells and a large population of CD45 cells expressed CD34, CD117, and stem cell antigen-1 molecules. When cultivated in selected media supplemented with hematopoietic cytokines, total dermal cells, lineage–, and/or highly enriched phenotypically defined cell subsets produced hematopoietic and nonhematopoietic colonies. When injected into lethally irradiated recipient mice, a small percentage of newborn dermal cells was able to migrate into hematopoietic tissues and the skin and survived through the 11-month monitoring period. Our ability to isolate a candidate autologous stem cell pool will make these cells ideal vehicles for genetic manipulation and gene therapy.

Key Words: dermis • mouse • single cell suspension • semisolid medium • hematopoietic cytokines







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