Modulation of human lymphocyte proliferation by FLFQPQRFamide, a FMRFamide-like peptide with anti-opiate properties

The octapeptide Phe-Leu-Phe-Gln-Pro-Gln-Arg-Phe-NH 2 (F8Fa), originally detected in mammalian brain by antisera raised against the invertebrate peptide Phe-Met-Arg-Phe-NH 2 (FMRFamide) is a neuropeptide able to antagonize the actions of both endogenous and exogenous opiates. Since it is well accepte...

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Veröffentlicht in:Journal of neuroimmunology 1992-05, Vol.38 (1), p.1-8
Hauptverfasser: Lecron, Jean-Claude, Minault, Martine, Allard, Michèle, Laforest, Pierre Goube de, Gombert, Jacques, Simonnet, Guy
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container_end_page 8
container_issue 1
container_start_page 1
container_title Journal of neuroimmunology
container_volume 38
creator Lecron, Jean-Claude
Minault, Martine
Allard, Michèle
Laforest, Pierre Goube de
Gombert, Jacques
Simonnet, Guy
description The octapeptide Phe-Leu-Phe-Gln-Pro-Gln-Arg-Phe-NH 2 (F8Fa), originally detected in mammalian brain by antisera raised against the invertebrate peptide Phe-Met-Arg-Phe-NH 2 (FMRFamide) is a neuropeptide able to antagonize the actions of both endogenous and exogenous opiates. Since it is well accepted that lymphocytes are targets for opiates, we have tested the effect of F8Fa on T cell proliferation from normal human peripheral blood lymphocytes. Our study shows that F8Fa exerts a concentration-dependent diphasic modulation of human T lymphocyte proliferation. Thus, despite a great variability between individuals, 10 −13 M F8Fa was found to enhance the proliferation of T cells induced by phytohemagglutinin or anti-CD2 monoclonal antibodies, whike 10 −7 M F8Fa inhibited T cell proliferation, without affecting cell viability. When F8Fa was tested on monocyte-depleted cell preparations, only the inhibitory effect was observed. These results indicate that F8Fa may stimulate T cells via monocytes, but may also directly inhibit T lymphocyte proliferation. Given the presence of F8Fa-like peptide in human plasma, we suggest that F8Fa may act as a neurohormone in the control of the immune system.
doi_str_mv 10.1016/0165-5728(92)90084-X
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Since it is well accepted that lymphocytes are targets for opiates, we have tested the effect of F8Fa on T cell proliferation from normal human peripheral blood lymphocytes. Our study shows that F8Fa exerts a concentration-dependent diphasic modulation of human T lymphocyte proliferation. Thus, despite a great variability between individuals, 10 −13 M F8Fa was found to enhance the proliferation of T cells induced by phytohemagglutinin or anti-CD2 monoclonal antibodies, whike 10 −7 M F8Fa inhibited T cell proliferation, without affecting cell viability. When F8Fa was tested on monocyte-depleted cell preparations, only the inhibitory effect was observed. These results indicate that F8Fa may stimulate T cells via monocytes, but may also directly inhibit T lymphocyte proliferation. 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subjects Anti-opiate peptide
Carbohydrate Sequence
Cell Division - drug effects
Dose-Response Relationship, Drug
F8Fa
FMRFamide
Humans
Kinetics
Molecular Sequence Data
Monocyte
Narcotic Antagonists - pharmacology
Neuropeptides - pharmacology
Oligopeptides - pharmacology
Peptides - pharmacology
T lymphocyte
T-Lymphocytes - cytology
title Modulation of human lymphocyte proliferation by FLFQPQRFamide, a FMRFamide-like peptide with anti-opiate properties
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