Muramyl dipeptide mimicry in the regulation of murine macrophage activation by serotonin

Muramyl peptides (MPs) are regulators of macrophage function. That the activities of MPs may be mediated by serotonin (5-HT) is supported by earlier work that demonstrated specific binding sites for MPs on macrophages that competitively bind 5-HT. Both mediators were also shown to enhance the produc...

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Veröffentlicht in:International journal of immunopharmacology 1995-03, Vol.17 (3), p.225,231-229,232
Hauptverfasser: Polanski, Malu, Vermeulen, Mary W., Wu, Jiayi, Karnovsky, Manfred L.
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Sprache:eng
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Zusammenfassung:Muramyl peptides (MPs) are regulators of macrophage function. That the activities of MPs may be mediated by serotonin (5-HT) is supported by earlier work that demonstrated specific binding sites for MPs on macrophages that competitively bind 5-HT. Both mediators were also shown to enhance the production of superoxide anion (an antibacterial agent) by these cells. We now report on two additional macrophage activation phenomena affected by 5-HT: phagocytosis and induction of tumor necrosis factorα (TNF) mRNA. Serotonin acts as a muramyl peptide-like agonist by increasing phagocytosis of tubercle bacilli by murine peritoneal macrophages, and as a partial agonist/antagonist in the induction of mRNA for tumor necrosis factor.These observations provide further evidence for a serotonergic involvement in some of the physiological responses to MPs.
ISSN:0192-0561
1879-3495
DOI:10.1016/0192-0561(94)00097-8