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http://purl.uniprot.org/citations/28960134http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/28960134http://www.w3.org/2000/01/rdf-schema#comment"The recruitment of endoplasmic reticulum (ER) components to dendritic cell (DC) phagosomes and endosomes is a crucial event to achieve efficient cross-presentation of exogenous antigens. We have previously identified the small GTPase Rab22a as a key regulator of MHC-I trafficking and antigen cross-presentation by DCs. In this study we show that low expression of Rab22a does not prevent the normal delivery of ER-derived proteins to DC phagosomes. In contrast, the presence of these proteins was diminished in endosomes labelled with a fluid phase marker. These observations were confirmed by a functional assay that assesses the translocation of a soluble protein to the cytosol. Interestingly, we also demonstrate that early endosomal maturation is altered in Rab22a deficient DCs. Our results indicate that Rab22a plays a major role in endosomal function and highlight the importance of studying the endocytic and phagocytic pathways separately in DCs."xsd:string
http://purl.uniprot.org/citations/28960134http://purl.org/dc/terms/identifier"doi:10.1080/21541248.2017.1384088"xsd:string
http://purl.uniprot.org/citations/28960134http://purl.uniprot.org/core/author"Croce C."xsd:string
http://purl.uniprot.org/citations/28960134http://purl.uniprot.org/core/author"Mayorga L.S."xsd:string
http://purl.uniprot.org/citations/28960134http://purl.uniprot.org/core/author"Cebrian I."xsd:string
http://purl.uniprot.org/citations/28960134http://purl.uniprot.org/core/date"2020"xsd:gYear
http://purl.uniprot.org/citations/28960134http://purl.uniprot.org/core/name"Small GTPases"xsd:string
http://purl.uniprot.org/citations/28960134http://purl.uniprot.org/core/pages"211-219"xsd:string
http://purl.uniprot.org/citations/28960134http://purl.uniprot.org/core/title"Differential requirement of Rab22a for the recruitment of ER-derived proteins to phagosomes and endosomes in dendritic cells."xsd:string
http://purl.uniprot.org/citations/28960134http://purl.uniprot.org/core/volume"11"xsd:string
http://purl.uniprot.org/citations/28960134http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/28960134
http://purl.uniprot.org/citations/28960134http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/28960134
http://purl.uniprot.org/uniprot/#_Q96IY7-mappedCitation-28960134http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28960134
http://purl.uniprot.org/uniprot/#_Q9UL26-mappedCitation-28960134http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28960134
http://purl.uniprot.org/uniprot/Q9UL26http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/28960134
http://purl.uniprot.org/uniprot/Q96IY7http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/28960134