ISOLATION AND CULTURE OF FETAL MURINE EPIDERMAL STEM CELLS IN VITRO AND rAAV2/eGFP GENETIC TRANSFECTION
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Department of Histology and Embryology, Harbin Medical University, Harbin 150086, China
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2006-06-23
2006-09-28
2007-10-06
Abstract
Objective To isolate,culture and identify epidermal stem cells(ESCs). The gene of enhanced green fluorescent protein(eGFP) was introduced via recombinant adeno-associated virus(rAAV) infection into the epidermal stem cells in vitro and the transfection efficiency under various tite of culture was determined. Methods 1. Getting fetal Wistar rats’dissociated single epidermal cells.2. Making laminin and CollagenⅣ the substitution of basal memrane,ESCs were isolated by adhering to murine laminin and CollagenⅣ.3. Epidermal stem cells were cultured in twenty-four-well plate,and cells number was controled 5×104 or so.After epidermal stem cells adhered to plate,diluted rAAV2/eGFP virus fluid with serum-free medium.The diluted rAAV2/eGFP virus fluid was added to the twenty-four-well plate according to the different MOI(viru gene/cells).The number of green fluorescence cells were counted under fluorescence microscope.The transfection efficiency was determined. Results 1. ESCs had better adhesive ability to laminin and higher colony formation efficiency(CFE) than that of keratinocytes.2. ESCs wer strongly positive with immunocytochemical staining of integrin β1 and keration 19(K19).3. After rAAV2/eGFP genetic transfection of ESCs,the positive cloning expressed highly eGFP gene along with time.Conclusion 1. These results suggest that rats’epidermal stem cells could been successfully isolated and enric