Cargando…

Modulation of TLR3/TLR4 inflammatory signaling by the GABA(B) receptor agonist baclofen in glia and immune cells: relevance to therapeutic effects in multiple sclerosis

The GABA(B) receptor agonist, baclofen, is used to treat muscle tightness and cramping caused by spasticity in a number of disorders including multiple sclerosis (MS), but its precise mechanism of action is unknown. Neuroinflammation drives the central pathology in MS and is mediated by both immunor...

Descripción completa

Detalles Bibliográficos
Autores principales: Crowley, Tadhg, Fitzpatrick, John-Mark, Kuijper, Teun, Cryan, John F., O’Toole, Orna, O’Leary, Olivia F., Downer, Eric J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4516894/
https://www.ncbi.nlm.nih.gov/pubmed/26283920
http://dx.doi.org/10.3389/fncel.2015.00284
_version_ 1782383116117082112
author Crowley, Tadhg
Fitzpatrick, John-Mark
Kuijper, Teun
Cryan, John F.
O’Toole, Orna
O’Leary, Olivia F.
Downer, Eric J.
author_facet Crowley, Tadhg
Fitzpatrick, John-Mark
Kuijper, Teun
Cryan, John F.
O’Toole, Orna
O’Leary, Olivia F.
Downer, Eric J.
author_sort Crowley, Tadhg
collection PubMed
description The GABA(B) receptor agonist, baclofen, is used to treat muscle tightness and cramping caused by spasticity in a number of disorders including multiple sclerosis (MS), but its precise mechanism of action is unknown. Neuroinflammation drives the central pathology in MS and is mediated by both immunoreactive glial cells and invading lymphocytes. Furthermore, a body of data indicates that the Toll-like receptor (TLR) family of innate immune receptors is implicated in MS progression. In the present study we investigated whether modulation of GABA(B) receptors using baclofen can exert anti-inflammatory effects by targeting TLR3 and(or) TLR4-induced inflammatory signaling in murine glial cells and human peripheral blood mononuclear cells (PBMCs) isolated from healthy control individuals and patients with the relapse-remitting (RR) form of MS. TLR3 and TLR4 stimulation promoted the nuclear sequestration of NF-κB and pro-inflammatory cytokine expression in murine glia, while TLR4, but not TLR3, promoted pro-inflammatory cytokine expression in PBMCs isolated from both healthy donors and RR-MS patients. Importantly, this effect was exacerbated in RR-MS patient immune cells. We present further evidence that baclofen dose-dependently attenuated TLR3- and TLR4-induced inflammatory signaling in primary glial cells. Pre-exposure of PBMCs isolated from healthy donors to baclofen attenuated TLR4-induced TNF-α expression, but did not affect TLR4-induced TNF-α expression in RR-MS patient PBMCs. Interestingly, mRNA expression of the GABA(B) receptor was reduced in PBMCs from RR-MS donors when compared to healthy controls, an effect that might contribute to the differential sensitivity to baclofen seen in healthy and RR-MS patient cells. Overall these findings indicate that baclofen differentially regulates TLR3 and TLR4 signaling in glia and immune cells, and offers insight on the role of baclofen in the treatment of neuroinflammatory disease states including MS.
format Online
Article
Text
id pubmed-4516894
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-45168942015-08-17 Modulation of TLR3/TLR4 inflammatory signaling by the GABA(B) receptor agonist baclofen in glia and immune cells: relevance to therapeutic effects in multiple sclerosis Crowley, Tadhg Fitzpatrick, John-Mark Kuijper, Teun Cryan, John F. O’Toole, Orna O’Leary, Olivia F. Downer, Eric J. Front Cell Neurosci Neuroscience The GABA(B) receptor agonist, baclofen, is used to treat muscle tightness and cramping caused by spasticity in a number of disorders including multiple sclerosis (MS), but its precise mechanism of action is unknown. Neuroinflammation drives the central pathology in MS and is mediated by both immunoreactive glial cells and invading lymphocytes. Furthermore, a body of data indicates that the Toll-like receptor (TLR) family of innate immune receptors is implicated in MS progression. In the present study we investigated whether modulation of GABA(B) receptors using baclofen can exert anti-inflammatory effects by targeting TLR3 and(or) TLR4-induced inflammatory signaling in murine glial cells and human peripheral blood mononuclear cells (PBMCs) isolated from healthy control individuals and patients with the relapse-remitting (RR) form of MS. TLR3 and TLR4 stimulation promoted the nuclear sequestration of NF-κB and pro-inflammatory cytokine expression in murine glia, while TLR4, but not TLR3, promoted pro-inflammatory cytokine expression in PBMCs isolated from both healthy donors and RR-MS patients. Importantly, this effect was exacerbated in RR-MS patient immune cells. We present further evidence that baclofen dose-dependently attenuated TLR3- and TLR4-induced inflammatory signaling in primary glial cells. Pre-exposure of PBMCs isolated from healthy donors to baclofen attenuated TLR4-induced TNF-α expression, but did not affect TLR4-induced TNF-α expression in RR-MS patient PBMCs. Interestingly, mRNA expression of the GABA(B) receptor was reduced in PBMCs from RR-MS donors when compared to healthy controls, an effect that might contribute to the differential sensitivity to baclofen seen in healthy and RR-MS patient cells. Overall these findings indicate that baclofen differentially regulates TLR3 and TLR4 signaling in glia and immune cells, and offers insight on the role of baclofen in the treatment of neuroinflammatory disease states including MS. Frontiers Media S.A. 2015-07-28 /pmc/articles/PMC4516894/ /pubmed/26283920 http://dx.doi.org/10.3389/fncel.2015.00284 Text en Copyright © 2015 Crowley, Fitzpatrick, Kuijper, Cryan, O’Toole, O’Leary and Downer. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Crowley, Tadhg
Fitzpatrick, John-Mark
Kuijper, Teun
Cryan, John F.
O’Toole, Orna
O’Leary, Olivia F.
Downer, Eric J.
Modulation of TLR3/TLR4 inflammatory signaling by the GABA(B) receptor agonist baclofen in glia and immune cells: relevance to therapeutic effects in multiple sclerosis
title Modulation of TLR3/TLR4 inflammatory signaling by the GABA(B) receptor agonist baclofen in glia and immune cells: relevance to therapeutic effects in multiple sclerosis
title_full Modulation of TLR3/TLR4 inflammatory signaling by the GABA(B) receptor agonist baclofen in glia and immune cells: relevance to therapeutic effects in multiple sclerosis
title_fullStr Modulation of TLR3/TLR4 inflammatory signaling by the GABA(B) receptor agonist baclofen in glia and immune cells: relevance to therapeutic effects in multiple sclerosis
title_full_unstemmed Modulation of TLR3/TLR4 inflammatory signaling by the GABA(B) receptor agonist baclofen in glia and immune cells: relevance to therapeutic effects in multiple sclerosis
title_short Modulation of TLR3/TLR4 inflammatory signaling by the GABA(B) receptor agonist baclofen in glia and immune cells: relevance to therapeutic effects in multiple sclerosis
title_sort modulation of tlr3/tlr4 inflammatory signaling by the gaba(b) receptor agonist baclofen in glia and immune cells: relevance to therapeutic effects in multiple sclerosis
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4516894/
https://www.ncbi.nlm.nih.gov/pubmed/26283920
http://dx.doi.org/10.3389/fncel.2015.00284
work_keys_str_mv AT crowleytadhg modulationoftlr3tlr4inflammatorysignalingbythegababreceptoragonistbaclofeningliaandimmunecellsrelevancetotherapeuticeffectsinmultiplesclerosis
AT fitzpatrickjohnmark modulationoftlr3tlr4inflammatorysignalingbythegababreceptoragonistbaclofeningliaandimmunecellsrelevancetotherapeuticeffectsinmultiplesclerosis
AT kuijperteun modulationoftlr3tlr4inflammatorysignalingbythegababreceptoragonistbaclofeningliaandimmunecellsrelevancetotherapeuticeffectsinmultiplesclerosis
AT cryanjohnf modulationoftlr3tlr4inflammatorysignalingbythegababreceptoragonistbaclofeningliaandimmunecellsrelevancetotherapeuticeffectsinmultiplesclerosis
AT otooleorna modulationoftlr3tlr4inflammatorysignalingbythegababreceptoragonistbaclofeningliaandimmunecellsrelevancetotherapeuticeffectsinmultiplesclerosis
AT olearyoliviaf modulationoftlr3tlr4inflammatorysignalingbythegababreceptoragonistbaclofeningliaandimmunecellsrelevancetotherapeuticeffectsinmultiplesclerosis
AT downerericj modulationoftlr3tlr4inflammatorysignalingbythegababreceptoragonistbaclofeningliaandimmunecellsrelevancetotherapeuticeffectsinmultiplesclerosis