STUDY OF THE HUMAN KERATINOCYTE ISOLATION METHODS AND IN-VITRO CULTURE TECHNIQUES IN A SINGLE LABORATORY

Citation
Eg. Fernandez et al., STUDY OF THE HUMAN KERATINOCYTE ISOLATION METHODS AND IN-VITRO CULTURE TECHNIQUES IN A SINGLE LABORATORY, European journal of plastic surgery, 21(7), 1998, pp. 353-357
Citations number
29
Categorie Soggetti
Surgery
ISSN journal
0930343X
Volume
21
Issue
7
Year of publication
1998
Pages
353 - 357
Database
ISI
SICI code
0930-343X(1998)21:7<353:SOTHKI>2.0.ZU;2-0
Abstract
The survey was conducted to analyze different human keratinocyte isola tion methods and in vitro culture techniques used in current practice. The aim was to find which would work best in our laboratory to obtain epidermal sheets suitable for grafting. The techniques for epidermal removal and keratinocyte isolation involve dispase II or trypsin solut ions at different concentrations and times. The number of cells and ce llular viability were measured from different origins and size samples . The main approaches developed for in vitro culture of keratinocytes include the use of serum-containing media and of a feeder-layer of let hally irradiated mouse fibroblasts, serum-free medium in the absence o f a feeder-layer and a commercially prepared serum-free medium. Other techniques include the use of different substrates such as laminin, fi bronectin, collagen IV or fibrin glue to obtain more complete differen tiation of epithelial sheets. The growth rate and cellular attachment have been studied using these media and support systems. In summary, f or the isolation of keratinocytes, the best results were obtained with 0.17% trypsin solution overnight. The best attachment and growth rate s of cell cultures have been obtained when using serum-containing medi um and a feeder-layer of lethally irradiated mouse fibroblasts.