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  • 标题:Murine hematopoietic blast colony-forming cells and their progeny have distinctive membrane marker profiles
  • 本地全文:下载
  • 作者:Donald Metcalf ; Ashley P. Ng ; Stephen J. L. Loughran
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2009
  • 卷号:106
  • 期号:45
  • 页码:19102-19107
  • DOI:10.1073/pnas.0910354106
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:Two distinct bone marrow-derived blast colony-forming cells can generate colonies of lineage-restricted progenitor cells in agar cultures of murine bone marrow. Both cell types selectively had a Kit+ ScaI+ phenotype distinguishing them from most lineage-restricted progenitor cells. Multicentric blast colony-forming cells stimulated by stem cell factor plus interleukin-6 (IL-6) (BL-CFC-S) were separable from most dispersed blast colony-forming cells stimulated by Flt3 ligand and IL-6 (BL-CFC-F) using CD34 and Flt3R probes. Multicentric BL-CFC-S cofractionated with colony-forming units, spleen (CFU-S) supporting the possibility that the 2 cells may be identical. The colony populations generated by BL-CFC-S were similar in their phenotype and proliferative capacity to progenitor cells in whole bone marrow but the progeny of BL-CFC-F were skewed with an abnormally high proportion of Kit- Flt3R+ cells whose clonogenic cells tended to generate only macrophage progeny. Both blast colony populations had a high percentage of GR1+ and Mac1+ cells but BL-CFC-F colonies also contained a significant population of B220+ and IL-7R+ cells relevant to the superior ability of BL-CFC-F colony cells to generate B lymphocytes and the known dependency of this process on Flt3 ligand and IL-7. The commitment events and phenotypic changes during the generation of differing progenitor cells in blast colonies can now be clonally analyzed in a convenient in vitro culture system.
  • 关键词:blast colonies ; lineage commitment ; hematopoietic stem cells
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