Neutrophilic NLRP3 inflammasome-dependent IL-1β secretion regulates the γδT17 cell response in respiratory bacterial infections.

Abstract : Traditionally regarded as simple foot soldiers of the innate immune response limited to the eradication of pathogens, neutrophils recently emerged as more complex cells endowed with a set of immunoregulatory functions. Using a model of invasive pneumococcal disease, we highlighted an unexpected key role for neutrophils as accessory cells in innate interleukin (IL)-17A production by lung resident Vγ6Vδ1(+) T cells via nucleotide-binding oligomerization domain receptor, pyrin-containing 3 (NLRP3) inflammasome-dependent IL-1β secretion. In vivo activation of the NLRP3 inflammasome in neutrophils required both host-derived and bacterial-derived signals. Elaborately, it relies on (i) alveolar macrophage-secreted TNF-α for priming and (ii) subsequent exposure to bacterial pneumolysin for activation. Interestingly, this mechanism can be translated to human neutrophils. Our work revealed the cellular and molecular dynamic events leading to γδT17 cell activation, and highlighted for the first time the existence of a fully functional NLRP3 inflammasome in lung neutrophils. This immune axis thus regulates the development of a protective host response to respiratory bacterial infections.Mucosal Immunology advance online publication, 4 January 2017; doi:10.1038/mi.2016.113.
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Article dans une revue
Mucosal Immunology, Nature Pub. Group, 2017
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http://www.hal.inserm.fr/inserm-01529364
Contributeur : Jean-Claude Sirard <>
Soumis le : mardi 30 mai 2017 - 16:18:11
Dernière modification le : mardi 3 juillet 2018 - 11:31:20

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  • HAL Id : inserm-01529364, version 1
  • PUBMED : 28051086

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M Hassane, D Demon, D Soulard, J Fontaine, Le Keller, et al.. Neutrophilic NLRP3 inflammasome-dependent IL-1β secretion regulates the γδT17 cell response in respiratory bacterial infections.. Mucosal Immunology, Nature Pub. Group, 2017. 〈inserm-01529364〉

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