Production of human tissue-engineered skin trilayer on a plasma-based hypodermis


Por: A. MONFORT, M. SORIANO-NAVARRO, J. GARCIA-VERDUGO and A. IZETA

Publicada: 1 jun 2013
Resumen:
Full thickness wounds require a dermal component to achieve functional permanent skin restoration. Currently available tissue-engineered skin substitutes lack a subcutaneous fat layer that would functionally contribute some of the mechanical and thermoregulatory properties of normal skin. To generate a trilayer engineered skin equivalent, we included bone marrow mesenchymal (BM-MSC) or adipose tissue-derived (ASC) stromal cells in a human plasma hydrogel exposed to adipogenic clues for three weeks. Approximately half of the cells differentiated under these conditions into mature adipocytes that survived for two years in culture with minimal medium change. In vitro generation of bona fide fully differentiated adipocytes was assessed by leptin secretion and ultrastructurally demonstrated through semithin to ultrathin sectioning and lipid staining with osmium tetroxide. Furthermore, presence of BM-MSCs or ASCs within the subcutaneous layer contributed to the epidermal differentiation program, with more proliferating basal cells depositing basal membrane proteins and differentiating into mature keratinocytes that were able to generate a pluristratified epithelium. In conclusion, we engineered a fully differentiated human skin trilayer that could present multiple applications such as use for in vitro drug absorption tests and regenerative therapies. Copyright (c) 2012 John Wiley & Sons, Ltd.

Filiaciones:
A. MONFORT:
 Fdn Inbiomed, San Sebastian, Spain

:
 CIBERNED, Unidad Mixta CIPF UVEG, Lab Morfol Celular, Valencia, Spain

:
 CIBERNED, Unidad Mixta CIPF UVEG, Lab Morfol Celular, Valencia, Spain

A. IZETA:
 Fdn Inbiomed, San Sebastian, Spain

 Hosp Donostia, Inst Biodonostia, San Sebastian 20014, Spain
ISSN: 19326254





Journal of Tissue Engineering and Regenerative Medicine
Editorial
WILEY, 111 RIVER ST, HOBOKEN 07030-5774, NJ, Reino Unido
Tipo de documento: Article
Volumen: 7 Número: 6
Páginas: 479-490
WOS Id: 000319831100007
ID de PubMed: 22294482

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