Neutrophil-derived CCL3 is essential for the rapid recruitment of dendritic cells to the site of Leishmania major inoculation in resistant mice.

Détails

ID Serval
serval:BIB_28B4C77E7436
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Neutrophil-derived CCL3 is essential for the rapid recruitment of dendritic cells to the site of Leishmania major inoculation in resistant mice.
Périodique
PLoS Pathogens
Auteur(s)
Charmoy M., Brunner-Agten S., Aebischer D., Auderset F., Launois P., Milon G., Proudfoot A.E., Tacchini-Cottier F.
ISSN
1553-7374[electronic], 1553-7366[linking]
Statut éditorial
Publié
Date de publication
2010
Volume
6
Numéro
2
Pages
e1000755
Langue
anglais
Résumé
Neutrophils are rapidly and massively recruited to sites of microbial infection, where they can influence the recruitment of dendritic cells. Here, we have analyzed the role of neutrophil released chemokines in the early recruitment of dendritic cells (DCs) in an experimental model of Leishmania major infection. We show in vitro, as well as during infection, that the parasite induced the expression of CCL3 selectively in neutrophils from L. major resistant mice. Neutrophil-secreted CCL3 was critical in chemotaxis of immature DCs, an effect lost upon CCL3 neutralisation. Depletion of neutrophils prior to infection, as well as pharmacological or genetic inhibition of CCL3, resulted in a significant decrease in DC recruitment at the site of parasite inoculation. Decreased DC recruitment in CCL3(-/-) mice was corrected by the transfer of wild type neutrophils at the time of infection. The early release of CCL3 by neutrophils was further shown to have a transient impact on the development of a protective immune response. Altogether, we identified a novel role for neutrophil-secreted CCL3 in the first wave of DC recruitment to the site of infection with L. major, suggesting that the selective release of neutrophil-secreted chemokines may regulate the development of immune response to pathogens.
Mots-clé
Animals, Chemokine CCL3/immunology, Chemokine CCL3/metabolism, Chemotaxis, Leukocyte/immunology, Dendritic Cells/immunology, Dendritic Cells/metabolism, Female, Flow Cytometry, Leishmania major/immunology, Leishmaniasis, Cutaneous/immunology, Leishmaniasis, Cutaneous/metabolism, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL, Neutrophils/immunology, Neutrophils/metabolism, Reverse Transcriptase Polymerase Chain Reaction
Pubmed
Web of science
Open Access
Oui
Création de la notice
02/02/2011 10:35
Dernière modification de la notice
20/08/2019 13:08
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