MSH RECEPTORS IN IMMORTALIZED HUMAN EPIDERMAL-KERATINOCYTES - A POTENTIAL MECHANISM FOR COORDINATE REGULATION OF THE EPIDERMAL-MELANIN UNIT

Receptors for melanotropin (MSH) were found to be expressed by immortalized primary human epidermal keratinocytes (RHEK-1). Using I-125 betaMSH as a probe, the MSH receptors from mouse melanoma cells and human keratinocytes were found to be remarkably similar. In each cell line, there were high and low affinity receptors, with the high affinity classes showing positive cooperativity. Competition of I-125-betaMSH for binding with non-radioactive MSH revealed similar profiles. Cross-linking studies, followed by gel electrophoresis and autoradiography, showed almost identical gel migration patterns. Both cell types expressed internal as well as plasma membrane binding sites. MSH receptors on both cell types were up-regulated by ultraviolet light and by MSH itself. Although the function of MSH receptors expressed by the immortalized keratinocytes is unknown, the results are consistent with recent reports that proliferation of epidermal keratinocytes is stimulated by MSH and that proopiomelanocortin genes are expresed in the epidermis. These results support a model in which keratinocytes and melanocytes, interacting in an ''epidermal-melanin unit,'' each respond to UV light signals with increased MSH receptor activity. (C) 1993 Wiley-Liss, Inc.