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http://purl.uniprot.org/citations/33534942http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/33534942http://www.w3.org/2000/01/rdf-schema#comment"Type 1 diabetes in non-obese diabetic (NOD) mice occurs when autoreactive T cells eliminate insulin producing pancreatic β cells. While extensively studied in T-cell receptor (TCR) transgenic mice, the contribution of alterations in thymic selection to the polyclonal T-cell pool in NOD mice is not yet resolved. The magnitude of signals downstream of TCR engagement with self-peptide directs the development of a functional T-cell pool, in part by ensuring tolerance to self. TCR interactions with self-peptide are also necessary for T-cell homeostasis in the peripheral lymphoid organs. To identify differences in TCR signal strength that accompany thymic selection and peripheral T-cell maintenance, we compared CD5 levels, a marker of basal TCR signal strength, on immature and mature T cells from autoimmune diabetes-prone NOD and -resistant B6 mice. The data suggest that there is no preferential selection of NOD thymocytes that perceive stronger TCR signals from self-peptide engagement. Instead, NOD mice have an MHC-dependent increase in CD4+ thymocytes and mature T cells that express lower levels of CD5. In contrast, T cell-intrinsic mechanisms lead to higher levels of CD5 on peripheral CD8+ T cells from NOD relative to B6 mice, suggesting that peripheral CD8+ T cells with higher basal TCR signals may have survival advantages in NOD mice. These differences in the T-cell pool in NOD mice may contribute to the development or progression of autoimmune diabetes."xsd:string
http://purl.uniprot.org/citations/33534942http://purl.org/dc/terms/identifier"doi:10.1111/imcb.12443"xsd:string
http://purl.uniprot.org/citations/33534942http://purl.uniprot.org/core/author"Dong M."xsd:string
http://purl.uniprot.org/citations/33534942http://purl.uniprot.org/core/author"Lesage S."xsd:string
http://purl.uniprot.org/citations/33534942http://purl.uniprot.org/core/author"Melichar H.J."xsd:string
http://purl.uniprot.org/citations/33534942http://purl.uniprot.org/core/author"Adegoke A."xsd:string
http://purl.uniprot.org/citations/33534942http://purl.uniprot.org/core/author"Anderson C.C."xsd:string
http://purl.uniprot.org/citations/33534942http://purl.uniprot.org/core/author"Lebel M.E."xsd:string
http://purl.uniprot.org/citations/33534942http://purl.uniprot.org/core/author"Audiger C."xsd:string
http://purl.uniprot.org/citations/33534942http://purl.uniprot.org/core/author"Valbon S.F."xsd:string
http://purl.uniprot.org/citations/33534942http://purl.uniprot.org/core/date"2021"xsd:gYear
http://purl.uniprot.org/citations/33534942http://purl.uniprot.org/core/name"Immunol Cell Biol"xsd:string
http://purl.uniprot.org/citations/33534942http://purl.uniprot.org/core/pages"656-667"xsd:string
http://purl.uniprot.org/citations/33534942http://purl.uniprot.org/core/title"CD5 levels reveal distinct basal T-cell receptor signals in T cells from non-obese diabetic mice."xsd:string
http://purl.uniprot.org/citations/33534942http://purl.uniprot.org/core/volume"99"xsd:string
http://purl.uniprot.org/citations/33534942http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/33534942
http://purl.uniprot.org/citations/33534942http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/33534942
http://purl.uniprot.org/uniprot/#_P13379-mappedCitation-33534942http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33534942
http://purl.uniprot.org/uniprot/#_Q3UP78-mappedCitation-33534942http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33534942
http://purl.uniprot.org/uniprot/#_Q91X69-mappedCitation-33534942http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33534942
http://purl.uniprot.org/uniprot/#_Q9ER20-mappedCitation-33534942http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33534942
http://purl.uniprot.org/uniprot/#_Q8C9H0-mappedCitation-33534942http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33534942
http://purl.uniprot.org/uniprot/Q91X69http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/33534942
http://purl.uniprot.org/uniprot/P13379http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/33534942