Binding of Anti-Inflammatoryα-Melanocyte-Stimulating-Hormone Peptides and Proinflammatory Cytokines to Receptors on Melanoma Cells
作者:
Krzysztof Lyson,
Giuliana Ceriani,
Akira Takashima,
Anna Catania,
James M. Lipton,
期刊:
Neuroimmunomodulation
(Karger Available online 1994)
卷期:
Volume 1,
issue 2
页码: 121-126
ISSN:1021-7401
年代: 1994
DOI:10.1159/000097145
出版商: S. Karger AG
关键词: Melanocytes;α-MSH11-13receptors;α-MSH analog;Saturation binding;Competitive binding;Interleukin-6;Interleukin-8;α-MSH1-13receptors
数据来源: Karger
摘要:
α-Melanocyte-stimulating hormone (α-MSH1-13), a peptide derived from proopiomelanocortin, has remarkable anti-inflammatory and antipyretic activities. This peptide and a tripeptide that forms the COOH-terminal portion of the molecule (α-MSH11-13; Lys Pro Val) inhibit inflammation when given centrally or peripherally Because of the similarity in their actions, the tripeptide has been presumed to be the amino acid message sequence underlying the effects ofα-MSH1-13. To test the possibility that the two peptides occupy the same receptors, competitive binding experiments were performed with B16 mouse melanoma cells that are known to haveα-MSH1-13receptors. In these experiments,α-MSH1-13did not inhibit binding of a radiolabelledα-MSH1-13analog. This finding suggests thatα-MSH1-13andα-MSH11-13exert their anti-inflammatory/antipyretic/anticytokine effects via stimulation of separate receptors. Becauseα-MSH inhibits the effects of several cytokines including inflammation caused by interleukin (IL)-6 and IL-8, the capacity of these cytokines to compete forα-MSH binding sites was tested. There was no evidence that these proinflammatory cytokines bind toα-MSH receptors on murine melanoma cells. Although further tests with host cells involved in inflammation are required, the latter result is the first evidence that the mechanism of anticytokine action ofα-MSH does not depend upon peptide/cytokine competition for binding sites.
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