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Issue title: Cell Therapy, Bioengineering and Regenerative Medicine, September 2008, Nancy, France
Article type: Research Article
Authors: Auxenfans, Céline; | Thépot, Amélie; | Justin, Virginie | Hautefeuille, Agnès | Shahabeddin, Lili | Damour, Odile; | Hainaut, Pierre
Affiliations: Banque de Tissus et Cellules des Hospices Civils de Lyon, Lyon, France | International Agency for Research on Cancer, Lyon, France
Note: [] Co-first-authors.
Note: [] Address for corespondence: Dr Odile Damour, Banque de Tissus et Cellules des Hospices Civils de Lyon, Hôpital E. Herriot, 69437 Lyon cedex 03, France. Tel.: +33 4 72 11 06 18; Fax:+33 4 72 11 96 49; E-mail: odile.damour@chu-lyon.fr.
Abstract: Large-scale culture of primary keratinocytes allows the production of large epidermal sheet surfaces for the treatment of extensive skin burns. This method is dependent upon the capacity to establish cultures of proliferating keratinocytes in conditions compatible with their clonal expansion while maintaining their capacity to differentiate into the typical squamous pattern of human epidermis. Feeder layers are critical in this process because the fibroblasts that compose this layer serve as a source of adhesion, growth and differentiation factors. In this report, we have characterise the expression patterns of p63 isoforms in primary keratinocytes cultured on two different feeder layer systems, murine 3T3 and human fibroblasts. We show that with the latter, keratinocytes express a higher ratio of ΔN to TAp63 isoform, in relation with higher clonogenic potential. These results indicate that human fibroblasts represent an adequate feeder layer system to support the culture of primary human keratinocytes.
Keywords: Feeder layer, 3T3 fibroblasts, human fibroblasts, keratinocytes culture, ΔN/TAp63
DOI: 10.3233/BME-2009-0601
Journal: Bio-Medical Materials and Engineering, vol. 19, no. 4-5, pp. 365-372, 2009
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