Neural crest–derived cells with stem cell features can be traced back to multiple lineages in the adult skin

Author:

Wong Christine E.1,Paratore Christian1,Dours-Zimmermann María T.2,Rochat Ariane3,Pietri Thomas4,Suter Ueli1,Zimmermann Dieter R.2,Dufour Sylvie4,Thiery Jean Paul4,Meijer Dies5,Beermann Friedrich6,Barrandon Yann3,Sommer Lukas1

Affiliation:

1. Department of Biology, Institute of Cell Biology, Swiss Federal Institute of Technology (ETH) Zurich, CH-8093 Zurich, Switzerland

2. Molecular Biology Laboratory, Department of Pathology, University Hospital of Zurich, CH-8091 Zurich, Switzerland

3. Laboratory of Stem Cell Dynamics, School of Life Sciences, Ecole Polytechnique Féderale de Lausanne and Lausanne University Hospital, CH-1015 Lausanne, Switzerland

4. UMR144, Centre National de la Recherche Scientifique, Institut Curie, 75248 Paris, Cedex 05, France

5. Department of Cell Biology and Genetics, Erasmus University Medical Center, 3000DR Rotterdam, Netherlands

6. Swiss Institute for Experimental Cancer Research, 1066 Epalinges, Switzerland

Abstract

Given their accessibility, multipotent skin-derived cells might be useful for future cell replacement therapies. We describe the isolation of multipotent stem cell–like cells from the adult trunk skin of mice and humans that express the neural crest stem cell markers p75 and Sox10 and display extensive self-renewal capacity in sphere cultures. To determine the origin of these cells, we genetically mapped the fate of neural crest cells in face and trunk skin of mouse. In whisker follicles of the face, many mesenchymal structures are neural crest derived and appear to contain cells with sphere-forming potential. In the trunk skin, however, sphere-forming neural crest–derived cells are restricted to the glial and melanocyte lineages. Thus, self-renewing cells in the adult skin can be obtained from several neural crest derivatives, and these are of distinct nature in face and trunk skin. These findings are relevant for the design of therapeutic strategies because the potential of stem and progenitor cells in vivo likely depends on their nature and origin.

Publisher

Rockefeller University Press

Subject

Cell Biology

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