Self-renewal and differentiation of interleukin-3-dependent multipotent stem cells are modulated by stromal cells and serum factors.
dc.contributor.author | Spooncer, Elaine | |
dc.contributor.author | Heyworth, Clare M | |
dc.contributor.author | Dunn, A | |
dc.contributor.author | Dexter, T Michael | |
dc.date.accessioned | 2010-11-22T18:15:23Z | |
dc.date.available | 2010-11-22T18:15:23Z | |
dc.date.issued | 1986 | |
dc.identifier.citation | Self-renewal and differentiation of interleukin-3-dependent multipotent stem cells are modulated by stromal cells and serum factors. 1986, 31 (2):111-8 Differentiation | en |
dc.identifier.issn | 0301-4681 | |
dc.identifier.pmid | 3091439 | |
dc.identifier.uri | http://hdl.handle.net/10541/116033 | |
dc.description.abstract | Interleukin-3 (IL-3)-dependent cell lines (FDCP-mix) were cloned and isolated from long-term bone-marrow cultures infected with src-MoMuLV. These cell lines have many of the characteristics of hematopoietic stem cells. Early isolates of the FDCP-mix cells form spleen colonies in irradiated mice and establish long-term hematopoiesis on irradiated marrow stroma in vitro in the absence of IL-3. These two properties of the cells are lost within 15 weeks of establishing the cell lines, but the cell lines retain their ability to differentiate in a multilineage response to hematopoietic growth factors and to hematopoietic stromal cells, as well as to self-renew in the presence of IL-3. The choice between differentiation and self-renewal in FDCP-mix cells can clearly be modified by culture conditions: in particular, cultures containing horse serum preferentially promote self-renewal, whereas cultures containing fetal calf serum preferentially promote differentiation. The FDCP-mix cell lines are not leukemic, nor do they contain the src oncogene. Their ability to respond to hematopoietic growth factors and stroma in a similar manner to normal hematopoietic cells makes them a valuable model for studying the regulation of hemopoietic cell self-renewal and differentiation. | |
dc.language.iso | en | en |
dc.subject | Haematopoietic Stem Cells | en |
dc.subject.mesh | Animals | |
dc.subject.mesh | Blood | |
dc.subject.mesh | Bone Marrow Cells | |
dc.subject.mesh | Cell Differentiation | |
dc.subject.mesh | Cell Division | |
dc.subject.mesh | Cell Line | |
dc.subject.mesh | Cells, Cultured | |
dc.subject.mesh | Colony-Forming Units Assay | |
dc.subject.mesh | Culture Media | |
dc.subject.mesh | Female | |
dc.subject.mesh | Growth Substances | |
dc.subject.mesh | Hematopoietic Stem Cells | |
dc.subject.mesh | Interleukin-3 | |
dc.subject.mesh | Lymphokines | |
dc.subject.mesh | Male | |
dc.subject.mesh | Mice | |
dc.subject.mesh | Mice, Inbred Strains | |
dc.title | Self-renewal and differentiation of interleukin-3-dependent multipotent stem cells are modulated by stromal cells and serum factors. | en |
dc.type | Article | en |
dc.identifier.eissn | 1432-0436 | |
dc.identifier.journal | Differentiation | en |
html.description.abstract | Interleukin-3 (IL-3)-dependent cell lines (FDCP-mix) were cloned and isolated from long-term bone-marrow cultures infected with src-MoMuLV. These cell lines have many of the characteristics of hematopoietic stem cells. Early isolates of the FDCP-mix cells form spleen colonies in irradiated mice and establish long-term hematopoiesis on irradiated marrow stroma in vitro in the absence of IL-3. These two properties of the cells are lost within 15 weeks of establishing the cell lines, but the cell lines retain their ability to differentiate in a multilineage response to hematopoietic growth factors and to hematopoietic stromal cells, as well as to self-renew in the presence of IL-3. The choice between differentiation and self-renewal in FDCP-mix cells can clearly be modified by culture conditions: in particular, cultures containing horse serum preferentially promote self-renewal, whereas cultures containing fetal calf serum preferentially promote differentiation. The FDCP-mix cell lines are not leukemic, nor do they contain the src oncogene. Their ability to respond to hematopoietic growth factors and stroma in a similar manner to normal hematopoietic cells makes them a valuable model for studying the regulation of hemopoietic cell self-renewal and differentiation. |