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Rapid Exercise-Induced Mobilization of Dendritic Cells Is Potentially Mediated by a Flt3L- and MMP-9-Dependent Process in Multiple Sclerosis

In healthy individuals, one exercise bout induces a substantial increase in the number of circulating leukocytes, while their function is transiently suppressed. The effect of one exercise bout in multiple sclerosis (MS) is less studied. Since recent evidence suggests a role of dendritic cells (DC)...

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Autores principales: Deckx, Nathalie, Wens, Inez, Nuyts, Amber H., Lee, Wai-Ping, Hens, Niel, Koppen, Gudrun, Goossens, Herman, Van Damme, Pierre, Berneman, Zwi N., Eijnde, Bert O., Cools, Nathalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4641936/
https://www.ncbi.nlm.nih.gov/pubmed/26604429
http://dx.doi.org/10.1155/2015/158956
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author Deckx, Nathalie
Wens, Inez
Nuyts, Amber H.
Lee, Wai-Ping
Hens, Niel
Koppen, Gudrun
Goossens, Herman
Van Damme, Pierre
Berneman, Zwi N.
Eijnde, Bert O.
Cools, Nathalie
author_facet Deckx, Nathalie
Wens, Inez
Nuyts, Amber H.
Lee, Wai-Ping
Hens, Niel
Koppen, Gudrun
Goossens, Herman
Van Damme, Pierre
Berneman, Zwi N.
Eijnde, Bert O.
Cools, Nathalie
author_sort Deckx, Nathalie
collection PubMed
description In healthy individuals, one exercise bout induces a substantial increase in the number of circulating leukocytes, while their function is transiently suppressed. The effect of one exercise bout in multiple sclerosis (MS) is less studied. Since recent evidence suggests a role of dendritic cells (DC) in the pathogenesis of MS, we investigated the effect of one combined endurance/resistance exercise bout on the number and function of DC in MS patients and healthy controls. Our results show a rapid increase in the number of DC in response to physical exercise in both MS patients and controls. Further investigation revealed that in particular DC expressing the migratory molecules CCR5 and CD62L were increased upon acute physical activity. This may be mediated by Flt3L- and MMP-9-dependent mobilization of DC, as demonstrated by increased circulating levels of Flt3L and MMP-9 following one exercise bout. Circulating DC display reduced TLR responsiveness after acute exercise, as evidenced by a less pronounced upregulation of activation markers, HLA-DR and CD86, on plasmacytoid DC and conventional DC, respectively. Our results indicate mobilization of DC, which may be less prone to drive inflammatory processes, following exercise. This may present a negative feedback mechanism for exercise-induced tissue damage and inflammation.
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spelling pubmed-46419362015-11-24 Rapid Exercise-Induced Mobilization of Dendritic Cells Is Potentially Mediated by a Flt3L- and MMP-9-Dependent Process in Multiple Sclerosis Deckx, Nathalie Wens, Inez Nuyts, Amber H. Lee, Wai-Ping Hens, Niel Koppen, Gudrun Goossens, Herman Van Damme, Pierre Berneman, Zwi N. Eijnde, Bert O. Cools, Nathalie Mediators Inflamm Research Article In healthy individuals, one exercise bout induces a substantial increase in the number of circulating leukocytes, while their function is transiently suppressed. The effect of one exercise bout in multiple sclerosis (MS) is less studied. Since recent evidence suggests a role of dendritic cells (DC) in the pathogenesis of MS, we investigated the effect of one combined endurance/resistance exercise bout on the number and function of DC in MS patients and healthy controls. Our results show a rapid increase in the number of DC in response to physical exercise in both MS patients and controls. Further investigation revealed that in particular DC expressing the migratory molecules CCR5 and CD62L were increased upon acute physical activity. This may be mediated by Flt3L- and MMP-9-dependent mobilization of DC, as demonstrated by increased circulating levels of Flt3L and MMP-9 following one exercise bout. Circulating DC display reduced TLR responsiveness after acute exercise, as evidenced by a less pronounced upregulation of activation markers, HLA-DR and CD86, on plasmacytoid DC and conventional DC, respectively. Our results indicate mobilization of DC, which may be less prone to drive inflammatory processes, following exercise. This may present a negative feedback mechanism for exercise-induced tissue damage and inflammation. Hindawi Publishing Corporation 2015 2015-10-29 /pmc/articles/PMC4641936/ /pubmed/26604429 http://dx.doi.org/10.1155/2015/158956 Text en Copyright © 2015 Nathalie Deckx et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Deckx, Nathalie
Wens, Inez
Nuyts, Amber H.
Lee, Wai-Ping
Hens, Niel
Koppen, Gudrun
Goossens, Herman
Van Damme, Pierre
Berneman, Zwi N.
Eijnde, Bert O.
Cools, Nathalie
Rapid Exercise-Induced Mobilization of Dendritic Cells Is Potentially Mediated by a Flt3L- and MMP-9-Dependent Process in Multiple Sclerosis
title Rapid Exercise-Induced Mobilization of Dendritic Cells Is Potentially Mediated by a Flt3L- and MMP-9-Dependent Process in Multiple Sclerosis
title_full Rapid Exercise-Induced Mobilization of Dendritic Cells Is Potentially Mediated by a Flt3L- and MMP-9-Dependent Process in Multiple Sclerosis
title_fullStr Rapid Exercise-Induced Mobilization of Dendritic Cells Is Potentially Mediated by a Flt3L- and MMP-9-Dependent Process in Multiple Sclerosis
title_full_unstemmed Rapid Exercise-Induced Mobilization of Dendritic Cells Is Potentially Mediated by a Flt3L- and MMP-9-Dependent Process in Multiple Sclerosis
title_short Rapid Exercise-Induced Mobilization of Dendritic Cells Is Potentially Mediated by a Flt3L- and MMP-9-Dependent Process in Multiple Sclerosis
title_sort rapid exercise-induced mobilization of dendritic cells is potentially mediated by a flt3l- and mmp-9-dependent process in multiple sclerosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4641936/
https://www.ncbi.nlm.nih.gov/pubmed/26604429
http://dx.doi.org/10.1155/2015/158956
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