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Arteriosclerosis, Thrombosis, and Vascular Biology
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Published Online
on February 5, 2009

Arteriosclerosis, Thrombosis, and Vascular Biology. 2009
Published online before print February 5, 2009, doi: 10.1161/ATVBAHA.108.178962
A more recent version of this article appeared on April 1, 2009
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Submitted on October 20, 2008
Accepted on January 26, 2009

Cell Therapy Based on Adipose Tissue-Derived Stromal Cells Promotes Physiological and Pathological Wound Healing

T. G. Ebrahimian ; F. Pouzoulet ; C. Squiban ; V. Buard ; M. André ; B. Cousin ; P. Gourmelon ; M. Benderitter ; L. Casteilla ; and R. Tamarat *

From the Institut de Radioprotection et de Surete Nucleaire IRSN, Service de Radiobiologie d'Epidemiologie (T.G.E, F.P., C.S., V.B., M.B., R.T.), Direction de la Radioprotection de l'Homme, Laboratoire de RadioPathologie, Fontenay-aux-Roses Cedex, France; and UMR 5241 CNRS UPS, IFR31 (M.A., B.C., L.C.), Toulouse, France.

* To whom correspondence should be addressed. E-mail: radia.tamarat{at}irsn.fr.

Objective—We hypothesized that adipose tissue may contain progenitors cells with cutaneous and angiogenic potential.

Methods and Results—Adipose tissue-derived stroma cells (ADSCs) were administrated to skin punched wounds of both nonirradiated and irradiated mice (20 Gy, locally). At day14, ADSCs promoted dermal wound healing and enhanced wound closure, viscolesticity, and collagen tissue secretion in both irradiated and nonirradiated mice. Interestingly, GFP-positive ADSCs incorporated in dermal and epidermal tissue in vivo and expressed epidermal markers K5 and K14. Cultured ADSCs in keratinocyte medium have been shown to differentiate into K5- and K14-positive cells and produced high levels of KGF. At Day 7, ADSCs also improved skin blood perfusion assessed by laser Doppler imaging, capillary density, and VEGF plasma levels in both irradiated and nonirradiated animals. GFP-positive ADSCs incorporated into capillary structures in vivo and expressed the endothelial cell marker CD31. Finally, in situ interphase fluorescence hybridization showed that a small number of ADSCs have the potential to fuse with endogenous keratinocytes.

Conclusion—ADSCs participate in dermal wound healing in physiological and pathological conditions by their ability to promote reepithelialization and angiogenesis. Hence, adipose lineage cells represent a new cell source for therapeutic dermal wound healing.