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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
1996-9-16
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pubmed:abstractText |
B cell development is influenced by interactions between B cell progenitors and stromal cells. The precise mechanisms by which these interactions regulate B cell differentiation are currently unknown. Flt3 ligand (FL) is a growth factor which stimulates the proliferation of stem cells and early progenitors. Mice deficient for the FLT3 receptor exhibit severe reductions in early B lymphoid progenitors. We have previously described a clonal assay in vitro which allows us to follow the entire B cell differentiation pathway from uncommitted progenitors to mature, immunoglobulin-secreting plasma cells. The growth factor combination of interleukin (IL)-11, mast cell growth factor (MGF) and IL-7 was shown to maintain the differentiation of these hematopoietic precursors into B cell progenitors capable of giving rise to functionally mature B cells in secondary cultures. Here, we show that FL in combination with IL-11 and IL-7 is sufficient to support the differentiation of uncommitted progenitors from day 10 yolk sac (AA4.1+) or day 12 fetal liver (AA4.1+ B220- Mac-1- Sca-1+) into the B lineage. The frequency of B cell progenitors obtained in these conditions was similar, if not better, than the frequency of B cell precursors that arose when cultured in IL-11+MGF+IL-7. Furthermore, the growth factor combination of IL-11+FL+ IL-7 was able to maintain the potential of bipotent precursors giving rise to both the B and myeloid lineages in secondary cultures. We also show that FL synergizes with IL-7 in the proliferation of committed B220+ pro-B cells and may contribute to the maintenance of an earlier pro-B cell population. Together, these results show that FL is important in supporting the differentiation and proliferation of early B cell progenitors in vitro.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Flt3 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-11,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-7,
http://linkedlifedata.com/resource/pubmed/chemical/Ligands,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor Protein-Tyrosine Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cell Surface,
http://linkedlifedata.com/resource/pubmed/chemical/Stem Cell Factor,
http://linkedlifedata.com/resource/pubmed/chemical/fms-Like Tyrosine Kinase 3
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0014-2980
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
26
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1504-10
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:8766553-Animals,
pubmed-meshheading:8766553-B-Lymphocyte Subsets,
pubmed-meshheading:8766553-B-Lymphocytes,
pubmed-meshheading:8766553-Cell Differentiation,
pubmed-meshheading:8766553-Drug Synergism,
pubmed-meshheading:8766553-Hematopoietic Stem Cells,
pubmed-meshheading:8766553-Interleukin-11,
pubmed-meshheading:8766553-Interleukin-7,
pubmed-meshheading:8766553-Ligands,
pubmed-meshheading:8766553-Mice,
pubmed-meshheading:8766553-Mice, Inbred C57BL,
pubmed-meshheading:8766553-Proto-Oncogene Proteins,
pubmed-meshheading:8766553-Receptor Protein-Tyrosine Kinases,
pubmed-meshheading:8766553-Receptors, Cell Surface,
pubmed-meshheading:8766553-Stem Cell Factor,
pubmed-meshheading:8766553-Yolk Sac,
pubmed-meshheading:8766553-fms-Like Tyrosine Kinase 3
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pubmed:year |
1996
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pubmed:articleTitle |
Flt3 ligand supports the differentiation of early B cell progenitors in the presence of interleukin-11 and interleukin-7.
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pubmed:affiliation |
Wellesley Hospital Research Institute, Toronto, Ontario, Canada. Ray@WHRI.ON.CA
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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