Source:http://linkedlifedata.com/resource/pubmed/id/20887955
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2010-10-4
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pubmed:databankReference | |
pubmed:abstractText |
Hematopoiesis requires the interaction of hematopoietic stem cells (HSCs) with various stromal microenvironments. Here, we examine the role of early B cell factor 2 (Ebf2), a transcription factor expressed in a subset of immature osteoblastic cells. Ebf2(-/-) mice show decreased frequencies of HSCs and lineage-committed progenitors. This defect is cell nonautonomous, as shown by the fact that transplantation of Ebf2-deficient bone marrow into wild-type hosts results in normal hematopoiesis. In coculture experiments, Ebf2(-/-) osteoblastic cells have reduced potential to support short-term proliferation of HSCs. Expression profiling of sorted Ebf2(-/-) osteoblastic cells indicated that several genes implicated in the maintenance of HSCs are downregulated relative to Ebf2(+/-) cells, whereas genes encoding secreted frizzled-related proteins are upregulated. Moreover, wild-type HSCs cocultured with Ebf2(-/-) osteoblastic cells show a reduced Wnt response relative to coculture with Ebf2(+/-) cells. Thus, Ebf2 acts as a transcriptional determinant of an osteoblastic niche that regulates the maintenance of hematopoietic progenitors, in part by modulating Wnt signaling.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1875-9777
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Elsevier Inc. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
8
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
496-507
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pubmed:meshHeading |
pubmed-meshheading:20887955-Animals,
pubmed-meshheading:20887955-B-Lymphocytes,
pubmed-meshheading:20887955-Basic Helix-Loop-Helix Transcription Factors,
pubmed-meshheading:20887955-Cell Differentiation,
pubmed-meshheading:20887955-Cell Lineage,
pubmed-meshheading:20887955-Gene Expression Regulation,
pubmed-meshheading:20887955-Hematopoiesis,
pubmed-meshheading:20887955-Hematopoietic Stem Cells,
pubmed-meshheading:20887955-Mice,
pubmed-meshheading:20887955-Mutation,
pubmed-meshheading:20887955-Osteoblasts,
pubmed-meshheading:20887955-Reverse Transcriptase Polymerase Chain Reaction
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pubmed:year |
2010
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pubmed:articleTitle |
Early B cell factor 2 regulates hematopoietic stem cell homeostasis in a cell-nonautonomous manner.
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pubmed:affiliation |
Department of Cellular and Molecular Immunology, Max Planck Institute of Immunobiology, 79108 Freiburg, Germany. matthias.kieslinger@helmholtz-muenchen.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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