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http://purl.uniprot.org/citations/19190245http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/19190245http://www.w3.org/2000/01/rdf-schema#comment"Protein 4.1R (4.1R) was first identified in red cells where it plays an important role in maintaining mechanical stability of red cell membrane. 4.1R has also been shown to be expressed in T cells, but its function has been unclear. In the present study, we use 4.1R-deficient mice to explore the role of 4.1R in T cells. We show that 4.1R is recruited to the immunologic synapse after T cell-antigen receptor (TCR) stimulation. We show further that CD4+ T cells of 4.1R-/-mice are hyperactivated and that they displayed hyperproliferation and increased production of interleukin-2 (IL-2) and interferon gamma (IFNgamma). The hyperactivation results from enhanced phosphorylation of LAT and its downstream signaling molecule ERK. The 4.1R exerts its effect by binding directly to LAT, and thereby inhibiting its phosphorylation by ZAP-70. Moreover, mice deficient in 4.1R display an elevated humoral response to immunization with T cell-dependent antigen. Thus, we have defined a hitherto unrecognized role for 4.1R in negatively regulating T-cell activation by modulating intracellular signal transduction."xsd:string
http://purl.uniprot.org/citations/19190245http://purl.org/dc/terms/identifier"doi:10.1182/blood-2008-10-182329"xsd:string
http://purl.uniprot.org/citations/19190245http://purl.uniprot.org/core/author"Guo X."xsd:string
http://purl.uniprot.org/citations/19190245http://purl.uniprot.org/core/author"Zhang X."xsd:string
http://purl.uniprot.org/citations/19190245http://purl.uniprot.org/core/author"Yu Y."xsd:string
http://purl.uniprot.org/citations/19190245http://purl.uniprot.org/core/author"Kang Q."xsd:string
http://purl.uniprot.org/citations/19190245http://purl.uniprot.org/core/author"An X."xsd:string
http://purl.uniprot.org/citations/19190245http://purl.uniprot.org/core/author"Mohandas N."xsd:string
http://purl.uniprot.org/citations/19190245http://purl.uniprot.org/core/author"Hughes R."xsd:string
http://purl.uniprot.org/citations/19190245http://purl.uniprot.org/core/author"Pei X."xsd:string
http://purl.uniprot.org/citations/19190245http://purl.uniprot.org/core/author"Heck S."xsd:string
http://purl.uniprot.org/citations/19190245http://purl.uniprot.org/core/author"Halverson G."xsd:string
http://purl.uniprot.org/citations/19190245http://purl.uniprot.org/core/date"2009"xsd:gYear
http://purl.uniprot.org/citations/19190245http://purl.uniprot.org/core/name"Blood"xsd:string
http://purl.uniprot.org/citations/19190245http://purl.uniprot.org/core/pages"6128-6137"xsd:string
http://purl.uniprot.org/citations/19190245http://purl.uniprot.org/core/title"Cytoskeletal protein 4.1R negatively regulates T-cell activation by inhibiting the phosphorylation of LAT."xsd:string
http://purl.uniprot.org/citations/19190245http://purl.uniprot.org/core/volume"113"xsd:string
http://purl.uniprot.org/citations/19190245http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/19190245
http://purl.uniprot.org/citations/19190245http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/19190245
http://purl.uniprot.org/uniprot/#_A0A068WAQ5-mappedCitation-19190245http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/19190245
http://purl.uniprot.org/uniprot/#_A0A068WAZ7-mappedCitation-19190245http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/19190245
http://purl.uniprot.org/uniprot/#_A0A1D5RLV1-mappedCitation-19190245http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/19190245
http://purl.uniprot.org/uniprot/#_A2A838-mappedCitation-19190245http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/19190245
http://purl.uniprot.org/uniprot/#_A2A839-mappedCitation-19190245http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/19190245