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dc.contributor.authorHope, J.C.en_US
dc.contributor.authorWerling, R.A.en_US
dc.contributor.authorCollins, R.A.en_US
dc.contributor.authorMertens, B.en_US
dc.contributor.authorHoward, C.J.en_US
dc.date.accessioned2013-07-03T05:26:09Zen_US
dc.date.available2013-07-03T05:26:09Zen_US
dc.identifier.urihttps://hdl.handle.net/10568/33165en_US
dc.titleFLT-3 Ligand in combination with bovine Granulocyte-Macrophage colony-stimulating factor and interleukin-4, promotes the growth of bovine bone marrow derived dendritic cellsen_US
dcterms.abstractCulture of bone marrow precursor cells with cytokines, including granulocyte - macrophage colony-stimulating factor (GM-CSF), interleukin-4 (IL-4) and the tyrosine kinase receptor binding proteins Flt-3 ligand (Flt3L) and stem-cell factor (SCF), has previously been shown, in both mouse and human, to result in the ,generation of large numbers of dendritic cells. We extend these findings to bovine dendritic cells. Culture of bovine bone marrow cells with GM-CSF, IL-4 and either Flt-3L or SCF - enhanced the generation of low buoyant-density dendritic cells. However, only the addition of Flt-3L to cells cultured with GM-CSI= and IL-4 was shown to increase the number of dendritic cells and induce the differentiation of dendritic cells with potent capacity to stimulate allogeneic T cells and resting CD4+ memory T cells. The effective ability to stimulate T cells was associated with the expression of major histocompatibility complex (MHC) class II molecules and CDSO/86 by dendritic cells. Bovine bone marrow derived dendritic cells appeared to be exclusively of myeloid origin because they expressed the myeloid-related antigens CD 14, MyD-1 and CD 1 lb.en_US
dcterms.accessRightsLimited Accessen_US
dcterms.bibliographicCitationScandinavian Journal of Immunology;51: 60-66en_US
dcterms.extentp. 60-66en_US
dcterms.issued2000-01en_US
dcterms.languageenen_US
dcterms.publisherWileyen_US
dcterms.subjectbovinaeen_US
dcterms.subjectcellsen_US
dcterms.subjectbone marrowen_US
dcterms.subjectgrowthen_US
dcterms.subjectinterleukinsen_US
dcterms.typeJournal Articleen_US
cg.subject.ilriCATTLEen_US
cg.subject.ilriGENETICSen_US
cg.subject.ilriLIVESTOCKen_US
cg.identifier.doihttps://doi.org/10.1046/j.1365-3083.2000.00646.xen_US
cg.journalScandinavian Journal of Immunologyen_US
cg.issn0300-9475en_US


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