Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12423
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dc.contributor.authorSmith, C Len
dc.contributor.authorPilarski, L Men
dc.contributor.authorEgerton, M Len
dc.contributor.authorWiley, J Sen
dc.date.accessioned2015-05-16T02:07:14Z
dc.date.available2015-05-16T02:07:14Z
dc.date.issued1989-11-01en
dc.identifier.citationBlood; 74(6): 2038-42en
dc.identifier.govdoc2529924en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/12423en
dc.description.abstractThe thymus is a site of active T-lymphoid cell proliferation and DNA synthesis. In this study, the capacity of human thymocytes for nucleoside transport was assessed both by cytosine arabinoside influx and by equilibrium binding of nitrobenzylmercaptopurine riboside (NBMPR), a specific ligand for the equilibrative nucleoside transporter of leukocytes. The proportion of freshly isolated thymocytes synthesizing DNA was 8.6% +/- 2.1% (n = 12) by 3H-thymidine labeling index and 7.8% +/- 2.9% (n = 4) S-phase cells by flow cytometric analysis of DNA content. In comparison, both methods gave proliferation S-phase values less than 1% for peripheral blood lymphocytes (PBLs). Thymocytes expressed a high density of specific NBMPR binding sites (26,068 +/- 8,776 sites per cell, n = 12) as compared with PBLs (1,123 +/- 553 sites per cell, n = 8). The initial influx of cytosine arabinoside into thymocytes was 14-fold greater than into PBLs, and in both cell types the influx of nucleoside was totally inhibited by 0.5 mumol/L NBMPR, which is known to inhibit the major equilibrative nucleoside transporter in white blood cells. Depletion of mature CD3+ cells from the thymocyte preparation by anti-CD3 antibody left a residual population with both increased labeling index and up to twofold greater density of NBMPR binding sites. When PBLs were cultured for 48 hours with the T-cell mitogen phytohemagglutinin, a 40-fold increase in labeling index was observed, together with a 30-fold increase in the density of specific NBMPR binding sites. Thus, fresh thymocytes from human thymus are actively proliferating and express high densities of a functional nucleoside transporter. The more immature cells in the thymocyte population which are proliferating more actively have a greater density of nucleoside transporters than the whole population. In contrast, mitotically inactive PBLs-have few nucleoside transporters, but after mitogenic stimulation PBLs express large numbers of this transmembrane molecule.en
dc.language.isoenen
dc.subject.otherAntigens, CD3en
dc.subject.otherAntigens, Differentiation, T-Lymphocyteen
dc.subject.otherBiological Transporten
dc.subject.otherCarrier Proteins.metabolismen
dc.subject.otherCell Divisionen
dc.subject.otherCell Separationen
dc.subject.otherHumansen
dc.subject.otherIn Vitro Techniquesen
dc.subject.otherLymphocytes.cytology.metabolismen
dc.subject.otherMembrane Proteins.metabolismen
dc.subject.otherNucleoside Transport Proteinsen
dc.subject.otherNucleosides.metabolismen
dc.subject.otherReceptors, Antigen, T-Cell.analysisen
dc.subject.otherThioinosine.metabolismen
dc.subject.otherThymus Gland.cytology.metabolismen
dc.titleNucleoside transport and proliferative rate in human thymocytes and lymphocytes.en
dc.typeJournal Articleen
dc.identifier.journaltitleBlooden
dc.identifier.affiliationDepartment of Haematology, Austin Hospital, Heidelberg, Victoria, Australiaen
dc.description.pages2038-42en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/2529924en
dc.type.austinJournal Articleen
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
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