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dc.contributor.authorDexter, T Michael
dc.contributor.authorTesta, Nydia G
dc.contributor.authorAllen, Terence D
dc.contributor.authorRutherford, T
dc.contributor.authorScolnick, E
dc.date.accessioned2011-07-12T17:34:26Z
dc.date.available2011-07-12T17:34:26Z
dc.date.issued1981-10
dc.identifier.citationMolecular and cell biologic aspects of erythropoiesis in long-term bone marrow cultures. 1981, 58 (4):699-707 Blooden
dc.identifier.issn0006-4971
dc.identifier.pmid7272501
dc.identifier.urihttp://hdl.handle.net/10541/135904
dc.description.abstractIn long-term marrow cultures, proliferation and differentiation of hemopoietic stem cells occurs for several months. Normally, only the most primitive erythroid progenitor cells are produced (the BFU-E). Following treatment with anemic mouse serum (AMS) or normal mouse serum plus erythropoietin, the BFU-E mature into CFU-E, which then go to produce mature nonnucleated red cells. This development is associated with the production of adult type hemoglobin. Furthermore, erythropoiesis and granulopoiesis occur in association with discrete cellular elements of the adherent cell layer in the long-term culture. Following treatment with AMS, erythropoiesis is enhanced while granulopoiesis is depressed, with no apparent competition at the stem cell or progenitor cell level.
dc.language.isoenen
dc.subject.meshAdipose Tissue
dc.subject.meshAnemia
dc.subject.meshAnimals
dc.subject.meshBone Marrow Cells
dc.subject.meshCell Communication
dc.subject.meshCells, Cultured
dc.subject.meshErythropoiesis
dc.subject.meshErythropoietin
dc.subject.meshGlobins
dc.subject.meshHematopoietic Stem Cells
dc.subject.meshMice
dc.subject.meshMice, Inbred DBA
dc.subject.meshTime Factors
dc.titleMolecular and cell biologic aspects of erythropoiesis in long-term bone marrow cultures.en
dc.typeArticleen
dc.contributor.departmentPaterson Laboratories, CHristie Hospital and Holt Radium Institute, Withington M20 9BX, Manchester Englanden
dc.identifier.journalBlooden
html.description.abstractIn long-term marrow cultures, proliferation and differentiation of hemopoietic stem cells occurs for several months. Normally, only the most primitive erythroid progenitor cells are produced (the BFU-E). Following treatment with anemic mouse serum (AMS) or normal mouse serum plus erythropoietin, the BFU-E mature into CFU-E, which then go to produce mature nonnucleated red cells. This development is associated with the production of adult type hemoglobin. Furthermore, erythropoiesis and granulopoiesis occur in association with discrete cellular elements of the adherent cell layer in the long-term culture. Following treatment with AMS, erythropoiesis is enhanced while granulopoiesis is depressed, with no apparent competition at the stem cell or progenitor cell level.


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