Enhanced Healing of Diabetic Wounds by Topical Administration of Adipose Tissue-Derived Stromal Cells Overexpressing Stromal-Derived Factor-1: Biodistribution and Engraftment Analysis by Bioluminescent Imaging
Author(s) -
Giuliana Di Rocco,
Antonietta Gentile,
Annalisa Antonini,
Francesca Ceradini,
Joseph C. Wu,
Maurizio C. Capogrossi,
Gabriele Toietta
Publication year - 2010
Publication title -
stem cells international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.205
H-Index - 64
eISSN - 1687-9678
pISSN - 1687-966X
DOI - 10.4061/2011/304562
Subject(s) - stromal cell , homing (biology) , wound healing , medicine , paracrine signalling , progenitor cell , adipose tissue , biodistribution , ex vivo , cancer research , bioluminescence imaging , stem cell , chemokine , pathology , in vivo , immunology , inflammation , luciferase , microbiology and biotechnology , biology , receptor , cell culture , ecology , transfection , genetics
Chronic ulcers represent a major health problem in diabetic patients resulting in pain and discomfort. Conventional therapy does not guarantee adequate wound repair. In diabetes, impaired healing is partly due to poor endothelial progenitor cells mobilisation and homing, with altered levels of the chemokine stromal-derived factor-1 (SDF-1) at the wound site. Adipose tissue-associated stromal cells (AT-SCs) can provide an accessible source of progenitor cells secreting proangiogenic factors and differentiating into endothelial-like cells. We demonstrated that topical administration of AT-SCs genetically modified ex vivo to overexpress SDF-1, promotes wound healing into diabetic mice. In particular, by in vivo bioluminescent imaging analysis, we monitored biodistribution and survival after transplantation of luciferase-expressing cells. In conclusion, this study indicates the therapeutic potential of AT-SCs administration in wound healing, through cell differentiation, enhanced cellular recruitment at the wound site, and paracrine effects associated with local growth-factors production.
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