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dc.contributor.authorSáez de Guinoa, Julia
dc.contributor.authorJimeno, Rebeca
dc.contributor.authorGaya, Mauro
dc.contributor.authorKipling, David
dc.contributor.authorGarzón, María J.
dc.contributor.authorDunn‐Walters, Deborah
dc.contributor.authorUbeda, Carles
dc.contributor.authorBarral, Patricia
dc.date.accessioned2024-11-05T19:27:14Z
dc.date.available2024-11-05T19:27:14Z
dc.date.issued2018-01-29
dc.identifier.urihttps://hdl.handle.net/1721.1/157494
dc.description.abstractIntestinal homeostasis relies on a continuous dialogue between the commensal bacteria and the immune system. Natural killer T (NKT) cells, which recognize CD1d‐restricted microbial lipids and self‐lipids, contribute to the regulation of mucosal immunity, yet the mechanisms underlying their functions remain poorly understood. Here, we demonstrate that NKT cells respond to intestinal lipids and CD11c+ cells (including dendritic cells (DCs) and macrophages) are essential to mediate lipid presentation within the gut ultimately controlling intestinal NKT cell homeostasis and activation. Conversely, CD1d and NKT cells participate in the control of the intestinal bacteria composition and compartmentalization, in the regulation of the IgA repertoire and in the induction of regulatory T cells within the gut. These changes in intestinal homeostasis require CD1d expression on DC/macrophage populations as mice with conditional deletion of CD1d on CD11c+ cells exhibit dysbiosis and altered immune homeostasis. These results unveil the importance of CD11c+ cells in controlling lipid‐dependent immunity in the intestinal compartment and reveal an NKT cell–DC crosstalk as a key mechanism for the regulation of gut homeostasis.en_US
dc.publisherNature Publishing Group UKen_US
dc.relation.isversionofhttps://doi.org/10.15252/embj.201797537en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNature Publishing Group UKen_US
dc.titleCD1d‐mediated lipid presentation by CD11c+ cells regulates intestinal homeostasisen_US
dc.typeArticleen_US
dc.identifier.citationThe EMBO Journal. 2018 Jan 29;37(5):EMBJ201797537en_US
dc.contributor.departmentRagon Institute of MGH, MIT and Harvarden_US
dc.relation.journalThe EMBO Journalen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2024-10-27T17:15:00Z
dc.language.rfc3066en
dc.rights.holderThe Author(s)
dspace.date.submission2024-10-27T17:15:00Z
mit.journal.volume37en_US
mit.journal.issue5en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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