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http://purl.uniprot.org/citations/10510343http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/10510343http://www.w3.org/2000/01/rdf-schema#comment"TCR alpha beta+ intestinal intraepithelial lymphocytes (IEL) can express either the typical CD8 alpha beta heterodimer or an unusual CD8 alpha alpha homodimer. Both types of CD8+ IEL require class I molecules for their differentiation, since they are absent in beta2m-/-mice. To gain insight into the role of class I molecules in forming TCR alpha beta+ CD8+ IEL populations, we have analyzed the IEL in mice deficient for either TAP, beta 2m, CD1, or K and D. We find that K-/-D-/-mice have TCR alpha beta+ CD8 alpha alpha+ IEL, although they are deficient for TCR alpha beta+ CD8 alpha beta+ cells. This indicates that at least some TCR alpha beta+ CD8 alpha alpha+ IEL require only nonclassical class I molecules for their development. Surprisingly, the TCR alpha beta+ CD8 alpha alpha+ IEL are significantly increased in K-/-D-/-mice, suggesting a complex interaction between CD8+ IEL and class I molecules that might include direct or indirect negative regulation by K and D, as well as positive effects mediated by nonclassical class I molecules."xsd:string
http://purl.uniprot.org/citations/10510343http://purl.uniprot.org/core/author"Kronenberg M."xsd:string
http://purl.uniprot.org/citations/10510343http://purl.uniprot.org/core/author"Cheroutre H."xsd:string
http://purl.uniprot.org/citations/10510343http://purl.uniprot.org/core/author"Gapin L."xsd:string
http://purl.uniprot.org/citations/10510343http://purl.uniprot.org/core/date"1999"xsd:gYear
http://purl.uniprot.org/citations/10510343http://purl.uniprot.org/core/name"J Immunol"xsd:string
http://purl.uniprot.org/citations/10510343http://purl.uniprot.org/core/pages"4100-4104"xsd:string
http://purl.uniprot.org/citations/10510343http://purl.uniprot.org/core/title"Cutting edge: TCR alpha beta+ CD8 alpha alpha+ T cells are found in intestinal intraepithelial lymphocytes of mice that lack classical MHC class I molecules."xsd:string
http://purl.uniprot.org/citations/10510343http://purl.uniprot.org/core/volume"163"xsd:string
http://purl.uniprot.org/citations/10510343http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/10510343
http://purl.uniprot.org/citations/10510343http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/10510343
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http://purl.uniprot.org/uniprot/#_A0A494BA33-mappedCitation-10510343http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/10510343
http://purl.uniprot.org/uniprot/#_A0A494BAT0-mappedCitation-10510343http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/10510343
http://purl.uniprot.org/uniprot/#_O19449-mappedCitation-10510343http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/10510343
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http://purl.uniprot.org/uniprot/#_P04223-mappedCitation-10510343http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/10510343