Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/8317
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dc.contributor.authorRinehart, John J.cat
dc.contributor.authorZanjani, Esmail D.cat
dc.contributor.authorNomdedeu, Benetcat
dc.contributor.authorGormus, Bobby J.cat
dc.contributor.authorKaplan, Manuel E.cat
dc.date.accessioned2009-05-15T08:48:48Z-
dc.date.available2009-05-15T08:48:48Z-
dc.date.issued1978cat
dc.identifier.issn0021-9738cat
dc.identifier.urihttps://hdl.handle.net/2445/8317-
dc.description.abstractErythroid burst forming units (BFU-E) are proliferative cells present in peripheral blood and bone marrow which may be precursors of the erythroid colony forming cell found in the bone marrow. To examine the possible role of monocyte-macrophages in the modulation of erythropoiesis, the effect of monocytes on peripheral blood BFU-E proliferation in response to erythropoietin was investigated in the plasma clot culture system. Peripheral blood mononuclear cells from normal human donors were separated into four fractions. Fraction-I cells were obtained from the interface of Ficoll-Hypaque gradients (20-30% monocytes; 60-80% lymphocytes); fraction-II cells were fraction-I cells that were nonadherent to plastic (2-10% monocytes; 90-98% lymphocytes); fraction-III cells were obtained by incubation of fraction-II cells with carbonyl iron followed by Ficoll-Hypaque centrifugation (>99% lymphocytes); and fraction-IV cells represented the adherent population of fraction-II cells released from the plastic by lidocaine (>95% monocytes). When cells from these fractions were cultured in the presence of erythropoietin, the number of BFU-E-derived colonies was inversely proportional to the number of monocytes present (r = ¿0.96, P < 0.001). The suppressive effect of monocytes on BFU-E proliferation was confirmed by admixing autologous purified monocytes (fraction-IV cells) with fraction-III cells. Monocyte concentrations of ¿20% completely suppressed BFU-E activity. Reduction in the number of plated BFU-E by monocyte dilution could not account for these findings: a 15% reduction in the number of fraction-III cells plated resulted in only a 15% reduction in colony formation. These results indicate that monocyte-macrophages may play a significant role in the regulation of erythropoiesis and be involved in the pathogenesis of the hypoproliferative anemias associated with infection and certain neoplasia in which increased monocyte activity and monopoiesis also occur.eng
dc.format.extent8 p.cat
dc.format.mimetypeapplication/pdfeng
dc.language.isoengeng
dc.publisherAmerican Society for Clinical Investigationcat
dc.relation.isformatofReproducció del document publicat a http://dx.doi.org/10.1172/JCI109227cat
dc.relation.urihttp://dx.doi.org/10.1172/JCI109227-
dc.rights(c) The American Society for Clinical Investigation, 1978cat
dc.sourceArticles publicats en revistes (Medicina)-
dc.subject.classificationEritropoesicat
dc.subject.classificationMacròfagscat
dc.subject.classificationInteracció cel·lularcat
dc.subject.otherErythropoiesiseng
dc.subject.otherMacrophages physiologyeng
dc.subject.otherMonocytes physiologyeng
dc.titleCell-Cell interaction in erythropoiesis: role of human monocyteseng
dc.typeinfo:eu-repo/semantics/articleeng
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec538508cat
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid711862-
Appears in Collections:Articles publicats en revistes (Medicina)

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