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The neuropeptide galanin modulates natural killer cell function.
- Source :
-
Neuropeptides [Neuropeptides] 2017 Aug; Vol. 64, pp. 109-115. Date of Electronic Publication: 2016 Nov 05. - Publication Year :
- 2017
-
Abstract
- Natural killer (NK) cells are part of the innate immune system and combat pathogens and tumors by secreting pro-inflammatory cytokines like interferon gamma (IFN-γ) and by their cytotoxic action. Galanin is a neuropeptide also expressed in peripheral tissue where it impacts several physiological functions, including inflammation. The effects of galanin are mediated via three receptors, GAL <subscript>1-3</subscript> . Since other neuropeptides have been shown to regulate NK cell activity, we investigated the potential of galanin to modulate human NK cell function. NK cells were isolated from human peripheral blood mononuclear cells. mRNA expression was analyzed by qRT-PCR. The dynamic mass redistribution of NK cells upon regulatory peptide stimulation was determined by label-free biochip technology. IFN-γ producing NK cells were identified by flow cytometry analysis and IFN-γ secretion was measured by ELISA. NK cell cytotoxicity was analyzed by flow cytometry via CD107a mobilization. NK cells were found to express the receptor GAL <subscript>2</subscript> but not GAL <subscript>1</subscript> , GAL <subscript>3</subscript> or galanin. Galanin per se did not affect the dynamic mass redistribution of NK cells, but significantly enhanced the response of NK cells to IL-18. Galanin significantly modulated the IFN-γ production of the CD56 <superscript>bright</superscript> NK cell population upon IL-12 and IL-18 stimulation. Furthermore, galanin significantly modulated the IL-12 and IL-18 stimulated IFN-γ secretion. NK cell cytotoxicity was not modulated by galanin treatment. Galanin can be classified as an immunomodulatory peptide as it is able to sensitize NK cells toward specific cytokines.<br /> (Copyright © 2016 Elsevier Ltd. All rights reserved.)
Details
- Language :
- English
- ISSN :
- 1532-2785
- Volume :
- 64
- Database :
- MEDLINE
- Journal :
- Neuropeptides
- Publication Type :
- Academic Journal
- Accession number :
- 27837916
- Full Text :
- https://doi.org/10.1016/j.npep.2016.11.002