Publication:
Autoimmune kidney disease and impaired engulfment of apoptotic cells in mice with macrophage peroxisome proliferator-activated receptor gamma or retinoid X receptor alpha deficiency.

dc.contributor.authorRoszer, Tamás
dc.contributor.authorMenéndez-Gutiérrez, María P
dc.contributor.authorLefterova, Martina I
dc.contributor.authorAlameda, Daniel
dc.contributor.authorNúñez, Vanessa
dc.contributor.authorLazar, Mitchell A
dc.contributor.authorFischer, Thierry
dc.contributor.authorRicote, Mercedes
dc.contributor.funderMinisterio de Ciencia e Innovación (España)es_ES
dc.contributor.funderFundación Genoma Españaes_ES
dc.contributor.funderFundación La Marató TV3es_ES
dc.contributor.funderMinisterio de Salud (España)es_ES
dc.contributor.funderMarie Curiees_ES
dc.contributor.funderFundación ProCNICes_ES
dc.date.accessioned2022-11-15T14:37:35Z
dc.date.available2022-11-15T14:37:35Z
dc.date.issued2011-01-01
dc.description.abstractAutoimmune glomerulonephritis is a common manifestation of systemic lupus erythematosus (SLE). In this study, we show that mice lacking macrophage expression of the heterodimeric nuclear receptors PPARγ or RXRα develop glomerulonephritis and autoantibodies to nuclear Ags, resembling the nephritis seen in SLE. These mice show deficiencies in phagocytosis and clearance of apoptotic cells, and they are unable to acquire an anti-inflammatory phenotype upon feeding of apoptotic cells, which is critical for the maintenance of self-tolerance. These results demonstrate that stimulation of PPARγ and RXRα in macrophages facilitates apoptotic cell engulfment, and they provide a potential strategy to avoid autoimmunity against dying cells and to attenuate SLE.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThis work was supported by grants from the Spanish Ministry of Science and Innovation (SAF2009-07466), the Fundación Genoma España, and Marató TV3 (to M.R.), and by grants from the Fundación Genoma España and the Spanish Ministry of Health (FIS PI052270) (to T.F.). T.R. is supported by the People Marie Curie Intra-European Fellowships Program. M.R. and T.F. are supported by the Ramón y Cajal Program. Centro Nacional de Investigaciones Cardiovasculares is supported by the Spanish Ministry of Science and Innovation and the ProCNIC Foundation. We thank Dr. Christian Hellriegel and Dr. Rubén Mota (Centro Nacional de Investigaciones Cardiovasculares [CNIC]), Roisin Brid Doohan (Histopathology Unit, CNIC), and Francisco Urbano Olmos and Covadonga Aguado Ballano (Transmission Electron Microscopy Laboratory, Universidad Autónoma, Madrid, Spain) for help and advice. We also thank Simon Bartlett for editorial assistance. The optical microscopy work described in this study was conducted at the Microscopy and Dynamic Imaging Unit, CNIC, Madrid, Spain.es_ES
dc.format.number1es_ES
dc.format.page621-31es_ES
dc.format.volume186es_ES
dc.identifier.citationJ Immunol . 2011 Jan 1;186(1):621-31.es_ES
dc.identifier.doi10.4049/jimmunol.1002230es_ES
dc.identifier.e-issn1550-6606es_ES
dc.identifier.journalJournal of immunology (Baltimore, Md. : 1950)es_ES
dc.identifier.pubmedID21135166es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/15156
dc.language.isoenges_ES
dc.publisherAmerican Association of Immunologists (AAI)es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/FIS/PI052270es_ES
dc.relation.publisherversion10.4049/jimmunol.1002230es_ES
dc.repisalud.institucionCNICes_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Señalización de los Receptores Nucleareses_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshAnimalses_ES
dc.subject.meshAntibodies, Antinucleares_ES
dc.subject.meshApoptosises_ES
dc.subject.meshFemalees_ES
dc.subject.meshLupus Nephritises_ES
dc.subject.meshMacrophageses_ES
dc.subject.meshMicees_ES
dc.subject.meshMice, Inbred C57BLes_ES
dc.subject.meshMice, Knockoutes_ES
dc.subject.meshMice, Transgenices_ES
dc.subject.meshPPAR gammaes_ES
dc.subject.meshPhagocytosises_ES
dc.subject.meshRetinoid X Receptor alphaes_ES
dc.subject.meshSelf Tolerancees_ES
dc.titleAutoimmune kidney disease and impaired engulfment of apoptotic cells in mice with macrophage peroxisome proliferator-activated receptor gamma or retinoid X receptor alpha deficiency.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublicationde41517f-d151-4bb6-8cf3-44f28ec51849
relation.isAuthorOfPublication.latestForDiscoveryde41517f-d151-4bb6-8cf3-44f28ec51849

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