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CD1d-mediated activation of group 3 innate lymphoid cells drives IL-22 production

dc.contributor.authorSáez de Guinoa, Julia
dc.contributor.authorJimeno Lumeras, Rebeca Gema
dc.contributor.authorFarhadi, Nazanin
dc.contributor.authorJervis, Peter J.
dc.contributor.authorCox, Liam R.
dc.contributor.authorBesra, Gurdyal S.
dc.contributor.authorBarral, Patricia
dc.date.accessioned2023-06-17T22:00:52Z
dc.date.available2023-06-17T22:00:52Z
dc.date.issued2017
dc.description.abstractInnate lymphoid cells (ILCs) are a heterogeneous family of immune cells that play a critical role in a variety of immune processes including host defence against infection, wound healing and tissue repair. Whether these cells are involved in lipid-dependent immunity remains unexplored. Here we show that murine ILCs from a variety of tissues express the lipid-presenting molecule CD1d, with group 3 ILCs (ILC3s) showing the highest level of expression. Within the ILC3 family, natural cytotoxicity triggering receptor (NCR) CCR6+ cells displayed the highest levels of CD1d. Expression of CD1d on ILCs is functionally relevant as ILC3s can acquire lipids in vitro and in vivo and load lipids on CD1d to mediate presentation to the T-cell receptor of invariant natural killer T (iNKT) cells. Conversely, engagement of CD1d in vitro and administration of lipid antigen in vivo induce ILC3 activation and production of IL-22. Taken together, our data expose a previously unappreciated role for ILCs in CD1d-mediated immunity, which can modulate tissue homeostasis and inflammatory responses.
dc.description.departmentDepto. de Biología Celular
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipUnión Europea. FP7
dc.description.sponsorshipUnión Europea. H2020
dc.description.sponsorshipMedical Research Council
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/43854
dc.identifier.doi10.15252/embr.201642412
dc.identifier.issn1469-3178
dc.identifier.officialurlhttp://embor.embopress.org/
dc.identifier.urihttps://hdl.handle.net/20.500.14352/17926
dc.issue.number1
dc.journal.titleEMBO reports
dc.language.isoeng
dc.page.final47
dc.page.initial39
dc.publisherEMBO Press
dc.relation.projectIDNKT CELLS IN MUCOSA (627391)
dc.relation.projectIDLIPID IMMUNITY (703639)
dc.relation.projectIDMR/ L008157/1; and G1001750
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.cdu576.3
dc.subject.keywordCD1d
dc.subject.keywordIL-22
dc.subject.keywordILC
dc.subject.keywordNKT cell
dc.subject.ucmBiología
dc.subject.ucmBiología celular (Biología)
dc.subject.unesco24 Ciencias de la Vida
dc.subject.unesco2407 Biología Celular
dc.titleCD1d-mediated activation of group 3 innate lymphoid cells drives IL-22 production
dc.typejournal article
dc.volume.number18
dspace.entity.typePublication

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