| Abstract: |
Epidermal cell cultures were grown in keratinocyte-conditioned medium for use as burn wound grafts; the melanocyte composition of the grafts was studied under a variety of conditions. Melanocytes were identified by immunohistochemistry based on a monoclonal antibody (MEL-5) that has previously been shown to react specifically with melanocytes. During the first 7 days of growth in primary culture, the total number of melanocytes in the epidermal cultures decreased to 10% of the number present in normal skin. Beginning on day 2 of culture, bipolar melanocytes were present at a mean cell density of 116 ± 2/mm2; the keratinocyte to melanocyte ratio was preserved during further primary culture and through three subpassages. Moreover, exposure of cultures to mild UVB irradiation stimulated the melanocytes to proliferate, suggesting that the melanocytes growing in culture maintained their responsiveness to external stimuli. When the sheets of cultured cells were enzymatically detached from the plastic culture flasks before grafting, melanocytes remained in the basal layer of cells as part of the graft applied to the patient. © 1990, by The Williams & Wilkins Co. |
| Keywords: |
human cell; conference paper; methodology; cells, cultured; cell division; epidermis; melanocyte; melanocytes; immunoenzyme techniques; antibodies, monoclonal; cell culture; cell count; epidemiology; ultraviolet rays; skin graft; normal human; skin transplantation; epidermis cell; burns; human; priority journal; support, non-u.s. gov't; support, u.s. gov't, p.h.s.
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