Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/109899
Title: Histamine modulates microglia function
Authors: Ferreira, Raquel 
Santos, Tiago 
Gonçalves, Joana 
Baltazar, Graça 
Ferreira, Lino 
Agasse, Fabienne 
Bernardino, Liliana 
Keywords: Histamine; Microglia; Inflammation; Histamine 4 receptor; Migration
Issue Date: 8-May-2012
Publisher: Springer Nature
Project: PTDC/SAU-NEU/104415/2008 
PTDC/SAU-NEU/101783/2008 
grant no. 96542, from the Calouste Gulbenkian Foundation 
L'Oréal-UNESCO Portugal for Women in Science 
MIT-Portugal 
PTDC/CTM/099659/2008 
Serial title, monograph or event: Journal of Neuroinflammation
Volume: 9
Abstract: Background: Histamine is commonly acknowledged as an inflammatory mediator in peripheral tissues, leaving its role in brain immune responses scarcely studied. Therefore, our aim was to uncover the cellular and molecular mechanisms elicited by this molecule and its receptors in microglia-induced inflammation by evaluating cell migration and inflammatory mediator release. Methods: Firstly, we detected the expression of all known histamine receptor subtypes (H1R, H2R, H3R and H4R), using a murine microglial cell line and primary microglia cell cultures from rat cortex, by real-time PCR analysis, immunocytochemistry and Western blotting. Then, we evaluated the role of histamine in microglial cell motility by performing scratch wound assays. Results were further confirmed using murine cortex explants. Finally, interleukin- 1beta (IL-1β) and tumor necrosis factor-alpha (TNF-α) levels were evaluated by ELISA measurements to determine the role of histamine on the release of these inflammatory mediators. Results: After 12 h of treatment, 100 μM histamine and 10 μg/ml histamine-loaded poly (lactic-co-glycolic acid) microparticles significantly stimulated microglia motility via H4R activation. In addition, migration involves α5β1 integrins, and p38 and Akt signaling pathways. Migration of microglial cells was also enhanced in the presence of lipopolysaccharide (LPS, 100 ng/ml), used as a positive control. Importantly, histamine inhibited LPS-stimulated migration via H4R activation. Histamine or H4R agonist also inhibited LPS-induced IL-1β release in both N9 microglia cell line and hippocampal organotypic slice cultures. Conclusions: To our knowledge, we are the first to show a dual role of histamine in the modulation of microglial inflammatory responses. Altogether, our data suggest that histamine per se triggers microglia motility, whereas histamine impedes LPS-induced microglia migration and IL-1β release. This last datum assigns a new putative antiinflammatory role for histamine, acting via H4R to restrain exacerbated microglial responses under inflammatory challenge, which could have strong repercussions in the treatment of CNS disorders accompanied by microgliaderived inflammation.
URI: http://hdl.handle.net/10316/109899
DOI: 10.1186/1742-2094-9-90
Rights: openAccess
Appears in Collections:I&D IBILI - Artigos em Revistas Internacionais
FMUC Medicina - Artigos em Revistas Internacionais
I&D CNC - Artigos em Revistas Internacionais

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