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The circadian clock in immune cells controls the magnitude of Leishmania parasite infection

The intracellular parasite Leishmania uses neutrophils and macrophages as host cells upon infection. These immune cells harbour their own intrinsic circadian clocks, known to influence many aspects of their functions. Therefore, we tested whether the host circadian clocks regulate the magnitude of L...

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Autores principales: Kiessling, Silke, Dubeau-Laramée, Geneviève, Ohm, Hyejee, Labrecque, Nathalie, Olivier, Martin, Cermakian, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589941/
https://www.ncbi.nlm.nih.gov/pubmed/28883509
http://dx.doi.org/10.1038/s41598-017-11297-8
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author Kiessling, Silke
Dubeau-Laramée, Geneviève
Ohm, Hyejee
Labrecque, Nathalie
Olivier, Martin
Cermakian, Nicolas
author_facet Kiessling, Silke
Dubeau-Laramée, Geneviève
Ohm, Hyejee
Labrecque, Nathalie
Olivier, Martin
Cermakian, Nicolas
author_sort Kiessling, Silke
collection PubMed
description The intracellular parasite Leishmania uses neutrophils and macrophages as host cells upon infection. These immune cells harbour their own intrinsic circadian clocks, known to influence many aspects of their functions. Therefore, we tested whether the host circadian clocks regulate the magnitude of Leishmania major infection in mice. The extent of parasitic infection varied over 24 h in bone marrow-derived macrophages in vitro and in two different in vivo models, footpad and peritoneal cavity infection. In vivo this was paralleled by time of day-dependent neutrophil and macrophage infiltration to the infection site and rhythmic chemokine expression. Thus, rhythmic parasitic infection observed in vivo was likely initiated by the circadian expression of chemoattractants and the subsequent rhythmic infiltration of neutrophils and macrophages. Importantly, all rhythms were abolished in clock-deficient macrophages and when mice lacking the circadian clock in immune cells were infected. Therefore we demonstrated a critical role for the circadian clocks in immune cells in modulating the magnitude of Leishmania infection. To our knowledge this is the first report showing that the circadian clock controls infection by protozoan parasites in mammals. Understanding the timed regulation of host-parasite interactions will allow developing better prophylactic and therapeutic strategies to fight off vector-borne diseases.
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spelling pubmed-55899412017-09-13 The circadian clock in immune cells controls the magnitude of Leishmania parasite infection Kiessling, Silke Dubeau-Laramée, Geneviève Ohm, Hyejee Labrecque, Nathalie Olivier, Martin Cermakian, Nicolas Sci Rep Article The intracellular parasite Leishmania uses neutrophils and macrophages as host cells upon infection. These immune cells harbour their own intrinsic circadian clocks, known to influence many aspects of their functions. Therefore, we tested whether the host circadian clocks regulate the magnitude of Leishmania major infection in mice. The extent of parasitic infection varied over 24 h in bone marrow-derived macrophages in vitro and in two different in vivo models, footpad and peritoneal cavity infection. In vivo this was paralleled by time of day-dependent neutrophil and macrophage infiltration to the infection site and rhythmic chemokine expression. Thus, rhythmic parasitic infection observed in vivo was likely initiated by the circadian expression of chemoattractants and the subsequent rhythmic infiltration of neutrophils and macrophages. Importantly, all rhythms were abolished in clock-deficient macrophages and when mice lacking the circadian clock in immune cells were infected. Therefore we demonstrated a critical role for the circadian clocks in immune cells in modulating the magnitude of Leishmania infection. To our knowledge this is the first report showing that the circadian clock controls infection by protozoan parasites in mammals. Understanding the timed regulation of host-parasite interactions will allow developing better prophylactic and therapeutic strategies to fight off vector-borne diseases. Nature Publishing Group UK 2017-09-07 /pmc/articles/PMC5589941/ /pubmed/28883509 http://dx.doi.org/10.1038/s41598-017-11297-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kiessling, Silke
Dubeau-Laramée, Geneviève
Ohm, Hyejee
Labrecque, Nathalie
Olivier, Martin
Cermakian, Nicolas
The circadian clock in immune cells controls the magnitude of Leishmania parasite infection
title The circadian clock in immune cells controls the magnitude of Leishmania parasite infection
title_full The circadian clock in immune cells controls the magnitude of Leishmania parasite infection
title_fullStr The circadian clock in immune cells controls the magnitude of Leishmania parasite infection
title_full_unstemmed The circadian clock in immune cells controls the magnitude of Leishmania parasite infection
title_short The circadian clock in immune cells controls the magnitude of Leishmania parasite infection
title_sort circadian clock in immune cells controls the magnitude of leishmania parasite infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589941/
https://www.ncbi.nlm.nih.gov/pubmed/28883509
http://dx.doi.org/10.1038/s41598-017-11297-8
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