Abstract
MC1R is recognized for its role in the regulation of melanin pigmentation. In addition, many investigators believe that it also plays a crucial role in immunomodulation (immunosuppression) and in melanogenesis-independent protective responses against ultraviolet radiation (UVR). Surprisingly, Wolnicka-Glubisz et al. have shown that loss of function in the MC1R has no effect on inflammatory responses and immunosuppression induced by UVR in C57BL/6 mice as well as on the degree of UVA-induced DNA damage in the epidermis and dermis. These findings, by challenging the existing dogmas on the precise role of MC1R in non-pigmentary responses to the UVR, mandate further research to either validate the presented data or to define to which degree these phenomena are restricted to the C57BL/6 mouse model or are applicable to other species including humans. The alternative target for immunomodulation is represented by MC3R. However, cutaneous expression of MC3R remains to be demonstrated.