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Updated: Apr 14, 2026

A Simplified and Efficient Method to Isolate Primary Human Keratinocytes from Adult Skin Tissue
Published on: August 25, 2018
Considerations in the improvement of human epidermal keratinocyte culture in vitro
Maryam Kaviani1, Bita Geramizadeh, Marjan Rahsaz
1From the Shiraz Transplant Research Center, Shiraz, Iran.
Objectives:
Large-scale expansion of epidermal keratinocytes is essential in the application of these cells for severe burn treatment in patients. Therefore, this study was designed to evaluate various conditions in the expansion of human epidermal keratinocytes.
Materials And Methods:
The epidermis was separated from the dermis of skin samples using dispase. The epidermis was trypsinized for keratinocyte isolation. Keratinocytes were cultured in various conditions, with or without a human dermal fibroblast feeder layer, mitomycin C treatment, and different culture media.
Results:
Our results suggest that keratinocytes cultured on a human dermal fibroblast feeder layer were grown for several passages. Extensive deformation and rapid deterioration were observed in the cultured cells without a feeder layer and in serum-free medium.
Conclusions:
Human dermal fibroblasts treated with mitomycin C can provide optimal conditions for proliferation of keratinocytes.
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