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http://purl.uniprot.org/citations/16225771http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/16225771http://www.w3.org/2000/01/rdf-schema#comment"We investigated CD19+CD34+ and CD19+CD34-B cells from cord blood (CB) and typical patients with B cell lineage acute and chronic lymphocytic leukemia (B-ALL and B-CLL) in terms of expression and functions of CXCR5/CXCL13 and CCR7/CCL19. CXCR5 and CCR7 were selectively frequent expressed on B-ALL, B-CLL and CB CD19+CD34+ B cells, but not on CD19+CD34-B cells. Instead of induction of impressive chemotactic responsiveness, CXCL13 and CCL19 together induced significant resistance to TNF-alpha-mediated apoptosis in B-ALL and B-CLL but not CB CD19+CD34+ B cells. B-ALL and B-CLL CD19+CD34+ B cells expressed elevated level of Paternally Expressed Gene 10 (PEG10), and CXCL13 and CCL19 together significantly up-regulated PEG10 expression in the cells. We found that CXCL13 and CCL19 together by means of activation of CXCR5 and CCR7 up-regulated PEG10 expression and function, subsequent stabilized caspase-3 and caspase-8 in B-ALL and B-CLL CD19+CD34+ B cells, and rescued the cells from TNF-alpha-mediated apoptosis. We suggested that normal lymphocytes, especially naive B and T cells, utilized CXCR5/CXCL13 and CCR7/CCL19 for migration, homing, maturation, and cell homeostasis as well as secondary lymphoid tissues organogenesis. Meanwhile certain malignant cells took advantages of CXCR5/CXCL13 and CCR7/CCL19 for infiltration, resistance to apoptosis, and inappropriate proliferation."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Jin Y."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Liu J."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Huang B."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Li Q."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Sun Z."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Tan J."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Wu Y."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Zhang Q."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Shen Q."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Zhang L."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Wu Q."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Yang M."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Zhang K."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Hu C."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Xiong J."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/author"Gao Q."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/date"2004"xsd:gYear
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/name"Cell Mol Immunol"xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/pages"280-294"xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/title"PEG10 activation by co-stimulation of CXCR5 and CCR7 essentially contributes to resistance to apoptosis in CD19+CD34+ B cells from patients with B cell lineage acute and chronic lymphocytic leukemia."xsd:string
http://purl.uniprot.org/citations/16225771http://purl.uniprot.org/core/volume"1"xsd:string
http://purl.uniprot.org/citations/16225771http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/16225771
http://purl.uniprot.org/citations/16225771http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/16225771