Zeitschriftenaufsatz
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2019
Galanin is a potent modulator of cytokine and chemokine expression in human macrophages
Autor:in
Koller, Andreas; Brunner, Susanne Maria; Bianchini, Rodolfo; Ramspacher, Andrea; Emberger, Michael; Sternberg, Felix; Schlager, Sandra; Kofler, Barbara
Publikationen als Autor:in / Herausgeber:in der Vetmeduni
Journal
Abstrakt
The regulatory peptide galanin is broadly distributed in the central- and peripheral nervous systems as well as in non-neuronal tissues, where it exerts its diverse physiological functions via three G-protein-coupled receptors (GAL(1-3)-R). Regulatory peptides are important mediators of the cross-communication between the nervous- and immune systems and have emerged as a focus of new therapeutics for a variety of inflammatory diseases. Studies on inflammatory animal models and immune cells revealed both pro- and anti-inflammatory functions of galanin. Here, we probed specific immune-related functions of the galanin system and found galanin and GAL(1)-R and GAL(2)-R mRNA to be expressed in a range of human immune cells. In particular, macrophages displayed differentiation- and polarization-dependent expression of galanin and its receptors. Exposure to exogenous galanin affected the cytokine/chemokine expression profile of macrophages differently, depending on their differentiation and polarization, and mainly modulated the expression of chemokines (CCL2, CCL3, CCL5 and CXCL8) and anti-inflammatory cytokines (TGF-beta, IL-10 and IL-1Ra), especially in type-1 macrophages. Cytokine/chemokine expression levels in interferon-gamma- and lipopolysaccharide-polarized macrophages were upregulated whereas in unpolarized macrophages they were downregulated upon galanin treatment for 20 hours. This study illuminates the regulation of important cytokines/chemokines in macrophages by galanin, depending on specific cell activation.
Schlagwörter
GENE-RELATED PEPTIDE; RECEPTOR-TYPE II; DENDRITIC CELLS; SUBSTANCE-P; INFLAMMATORY CYTOKINES; ACTIVATED MACROPHAGES; NEUROPEPTIDES; SPEXIN; SECRETION; POLARIZATION
Dokumententyp
Originalarbeit
CC Lizenz
CCBY
Open Access Type
Gold
ISSN/eISSN
2045-2322 -
WoS ID
PubMed ID