<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>107(37)</volume><submitter>Metcalf D</submitter><pubmed_abstract>Murine hematopoietic blast colony-forming cells (BL-CFCs) are able to generate up to 30,000 progeny blast cells within 10 d in agar cultures. Contained in these populations are large numbers of lineage-committed progenitor cells in the granulocytic and macrophage lineages. Sequential analyses of blast colonies revealed that self-generation of BL-CFCs occurs but is surprisingly late in clonal expansion, as is the emergence of progenitor cells committed to megakaryocytic and eosinophil lineages. Self-generating BL-CFCs were highly enriched in lineage(-) Kit(+) Sca1(+) CD34(-) Flt3R(-) populations, and colonies generated by such cells contained colony-forming units-spleen and formed erythroid and lymphoid progeny in vivo. The data suggest the existence of a hierarchical structure in BL-CFC populations with at least a subset being cells assayable as colony-forming units-spleen. Because BL-CFCs can self-generate and are able to generate lymphoid and myeloid populations, BL-CFCs appear to be ideal cells in which to analyze the processes of self-generation and lineage commitment in clonal in vitro cultures.</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>16257-61</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2941309</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Multipotential hematopoietic blast colony-forming cells exhibit delays in self-generation and lineage commitment.</pubmed_title><pmcid>PMC2941309</pmcid><pubmed_authors>Metcalf D</pubmed_authors><pubmed_authors>Mifsud S</pubmed_authors><pubmed_authors>Di Rago L</pubmed_authors><pubmed_authors>Ng A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multipotential hematopoietic blast colony-forming cells exhibit delays in self-generation and lineage commitment.</name><description>Murine hematopoietic blast colony-forming cells (BL-CFCs) are able to generate up to 30,000 progeny blast cells within 10 d in agar cultures. Contained in these populations are large numbers of lineage-committed progenitor cells in the granulocytic and macrophage lineages. Sequential analyses of blast colonies revealed that self-generation of BL-CFCs occurs but is surprisingly late in clonal expansion, as is the emergence of progenitor cells committed to megakaryocytic and eosinophil lineages. Self-generating BL-CFCs were highly enriched in lineage(-) Kit(+) Sca1(+) CD34(-) Flt3R(-) populations, and colonies generated by such cells contained colony-forming units-spleen and formed erythroid and lymphoid progeny in vivo. The data suggest the existence of a hierarchical structure in BL-CFC populations with at least a subset being cells assayable as colony-forming units-spleen. Because BL-CFCs can self-generate and are able to generate lymphoid and myeloid populations, BL-CFCs appear to be ideal cells in which to analyze the processes of self-generation and lineage commitment in clonal in vitro cultures.</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Sep</publication><modification>2021-02-21T00:13:31Z</modification><creation>2019-03-27T00:34:12Z</creation></dates><accession>S-EPMC2941309</accession><cross_references><pubmed>20805490</pubmed><doi>10.1073/pnas.1011881107</doi></cross_references></HashMap>