The two mouse melanoma cell lines B16-F1 and B16-G4F retain their mela
nogenic capacity when cultured in vitro. Melanotropic peptides such as
alpha-melanocyte-stimulating hormone (alpha-MSH) induce formation and
release of melanin pigment in B16-F1 cells. In contrast, B16-G4F cell
s do not respond to alpha-MSH. Using receptor-binding analysis and pho
toaffinity crosslinking we demonstrate that the lack of response of B1
6-G4F cells to alpha-MSH is due to the absence of functional MSH recep
tors from the cell surface. Northern blot analysis of receptor mRNA re
vealed that MSH receptor mRNA is not expressed in B16-G4F cells. These
cells represent a new tool for the study of signal pathways related t
o the control of melanogenesis in melanoma cells.