Abstract
Binding assays using 2-[125I]iodomelatonin revealed high-affinity, guanosine 5'-O-(3-thiotriphosphate) sensitive, melatonin binding sites (B(max) 1.1 fmol/mg protein) in the human embryonic kidney cell line HEK293. Competition studies using the selective melatonin receptor antagonist luzindole and RT-PCR techniques identified these sites as human Mel1a melatonin receptors. Challenge of HEK293 cells with 1 microM melatonin had no effect on forskolin stimulated cyclic AMP levels, whereas in HEK293 cells engineered to stably over-express the human Mel1a melatonin receptor (B(max) > 400 fmol/mg protein) melatonin dose-dependently inhibited stimulated cyclic AMP levels (IC50 7.7 pM). These data may indicate that certain tissues, expressing low levels of G protein-coupled melatonin receptors, do not display melatonin mediated inhibition of cAMP.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Binding, Competitive
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Cell Line
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Colforsin / pharmacology
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Cyclic AMP / metabolism
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GTP-Binding Proteins / metabolism*
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Genomic Library
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Humans
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Kidney / cytology
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Kidney / embryology
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Kidney / metabolism*
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Melatonin / analogs & derivatives
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Melatonin / metabolism*
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RNA, Messenger / genetics
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Receptors, Cell Surface / genetics
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Receptors, Cell Surface / metabolism*
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Receptors, Cytoplasmic and Nuclear / genetics
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Receptors, Cytoplasmic and Nuclear / metabolism*
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Receptors, Melatonin
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Sequence Analysis, DNA
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Serotonin / analogs & derivatives
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Serotonin / metabolism
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Signal Transduction
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Tryptamines / metabolism
Substances
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RNA, Messenger
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Receptors, Cell Surface
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Receptors, Cytoplasmic and Nuclear
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Receptors, Melatonin
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Tryptamines
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luzindole
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Colforsin
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Serotonin
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2-iodomelatonin
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Cyclic AMP
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GTP-Binding Proteins
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Melatonin
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N-acetylserotonin
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6-hydroxymelatonin