Endogenous melanin-concentrating hormone receptor SLC-1 in human melanoma SK-MEL-37 cells
Citation
Y. Saito et al., Endogenous melanin-concentrating hormone receptor SLC-1 in human melanoma SK-MEL-37 cells, BIOC BIOP R, 289(1), 2001, pp. 44-50
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
SICI code
0006-291X(20011123)289:1<44:EMHRSI>2.0.ZU;2-M
Abstract
Melanin-concentrating hormone (MCH) is a hypothalamic neuropeptide that reg
ulates several physiological functions. The orphan G protein-coupled recept
ors SLC-1 and MCHR2 were recently found to bind MCH with high affinity. We
show here that the human melanoma cell line SK-MEL-37 expresses SLC-1 mRNA
but not MCHR2 by RT-PCR analysis and immunofluorescence studies. Using Chin
ese hamster ovary cells and 293 cells overexpressing SLC-1 by cDNA transfec
tion, it was shown that SLC-1 coupled to both G alpha (i)/G alpha (o) and G
alpha (q) proteins. In SK-MEL-37 cells, MCH inhibited forskolin-stimulated
cyclic AMP accumulation and induced mitogen-activated protein kinase (MAPK
) in a pertussis toxin- (PTX) -sensitive manner. The MAPK activity leads to
the production of phosphorylated forms of p42/p44 MAPK. However, an increa
se in the intracellular free Ca2+ concentration was not elicited by MCH in
SK-MEL-37 cells. These results show that SLC-1 is coupled only to PTX-sensi
tive Gai/Gao in SK-MEL-37 cells. This study provides for the first time a s
kin-derived cellular model to analyze the molecular mechanism of the MCH si
gnaling pathway. (C) 2001 Academic Press.