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dc.contributor.author
Barrera Avalos, Carlos  
dc.contributor.author
Briceño, Pedro  
dc.contributor.author
Valdés, Daniel  
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Imarai, Mónica  
dc.contributor.author
Leiva Salcedo, Elías  
dc.contributor.author
Rojo, Leonel E.  
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Milla, Luis A.  
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Huidobro Toro, Juan Pablo  
dc.contributor.author
Robles Planells, Claudia  
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Escobar, Alejandro  
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Di Virgilio, Francesco  
dc.contributor.author
Moron, Victor Gabriel  
dc.contributor.author
Sauma, Daniela  
dc.contributor.author
Acuña Castillo, Claudio  
dc.date.available
2023-01-13T19:56:24Z  
dc.date.issued
2021-11-26  
dc.identifier.citation
Barrera Avalos, Carlos; Briceño, Pedro; Valdés, Daniel; Imarai, Mónica; Leiva Salcedo, Elías; et al.; P2X7 receptor is essential for cross-dressing of bone marrow-derived dendritic cells; Elsevier Inc.; iScience; 24; 12; 26-11-2021; 1-19  
dc.identifier.uri
http://hdl.handle.net/11336/184734  
dc.description.abstract
T cell activation requires the processing and presentation of antigenic peptides in the context of a major histocompatibility complex (MHC complex). Cross-dressing is a non-conventional antigen presentation mechanism, involving the transfer of preformed peptide/MHC complexes from whole cells, such as apoptotic cells (ACs) to the cell membrane of professional antigen-presenting cells (APCs), such as dendritic cells (DCs). This is an essential mechanism for the induction of immune response against viral antigens, tumors, and graft rejection, which until now has not been clarified. Here we show for first time that the P2X7 receptor (P2X7R) is crucial to induce cross-dressing between ACs and Bone-Marrow DCs (BMDCs). In controlled ex vivo assays, we found that the P2X7R in both ACs and BMDCs is required to induce membrane and fully functional peptide/MHC complex transfer to BMDCs. These findings show that acquisition of ACs-derived preformed antigen/MHC-I complexes by BMDCs requires P2X7R expression.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier Inc.  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
CELL BIOLOGY  
dc.subject
IMMUNE RESPONSE  
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IMMUNE SYSTEM  
dc.subject.classification
Inmunología  
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Medicina Básica  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
P2X7 receptor is essential for cross-dressing of bone marrow-derived dendritic cells  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2022-09-21T10:55:05Z  
dc.identifier.eissn
2589-0042  
dc.journal.volume
24  
dc.journal.number
12  
dc.journal.pagination
1-19  
dc.journal.pais
Estados Unidos  
dc.description.fil
Fil: Barrera Avalos, Carlos. Universidad de Santiago de Chile; Chile  
dc.description.fil
Fil: Briceño, Pedro. Universidad de Chile; Chile  
dc.description.fil
Fil: Valdés, Daniel. Universidad de Santiago de Chile; Chile  
dc.description.fil
Fil: Imarai, Mónica. Universidad de Santiago de Chile; Chile  
dc.description.fil
Fil: Leiva Salcedo, Elías. Universidad de Santiago de Chile; Chile  
dc.description.fil
Fil: Rojo, Leonel E.. Universidad de Santiago de Chile; Chile  
dc.description.fil
Fil: Milla, Luis A.. Universidad de Santiago de Chile; Chile  
dc.description.fil
Fil: Huidobro Toro, Juan Pablo. Universidad de Santiago de Chile; Chile  
dc.description.fil
Fil: Robles Planells, Claudia. Universidad de Santiago de Chile; Chile  
dc.description.fil
Fil: Escobar, Alejandro. Universidad de Chile; Chile  
dc.description.fil
Fil: Di Virgilio, Francesco. Università di Ferrara; Italia  
dc.description.fil
Fil: Moron, Victor Gabriel. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Bioquímica Clínica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina  
dc.description.fil
Fil: Sauma, Daniela. Universidad de Chile; Chile  
dc.description.fil
Fil: Acuña Castillo, Claudio. Universidad de Santiago de Chile; Chile  
dc.journal.title
iScience  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.isci.2021.103520