Item Type: | Article |
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Title: | Long-term, multilineage hematopoiesis occurs in the combined absence of beta-catenin and gamma-catenin |
Creators Name: | Jeannet, G., Scheller, M., Scarpellino, L., Duboux, S., Gardiol, N., Back, J., Kuttler, F., Malanchi, I., Birchmeier, W., Leutz, A., Huelsken, J. and Held, W. |
Abstract: | The canonical Wnt signaling pathway plays key roles in stem cell maintenance, progenitor cell expansion and lineage decisions. Transcriptional responses induced by Wnt depend on the association of either beta-catenin or gamma-catenin with TCF/LEF transcription factors. Here we show that hematopoiesis, including thymopoiesis, is normal in the combined absence of beta- and gamma-catenin. Double-deficient hematopoietic stem cells (HSCs) maintain long-term repopulation capacity and multi lineage differentiation potential. Unexpectedly, two independent ex vivo reporter gene assays show that Wnt signal transmission is maintained in double-deficient HSCs, thymocytes, or peripheral T cells. In contrast, Wnt signaling is strongly reduced in thymocytes lacking TCF-1 or in non-hematopoietic cells devoid of beta-catenin. These data provide the first evidence that hematopoietic cells can transduce canonical Wnt signals in the combined absence of beta- and gamma-catenin. |
Keywords: | Bone Marrow Cells, Cell Lineage, Hematopoiesis, Hematopoietic Stem Cells, Hybridomas, Signal Transduction, Spleen, T-Lymphocytes, Thymus Gland, Wnt Proteins, beta Catenin, gamma Catenin, Animals, Mice |
Source: | Blood |
ISSN: | 0006-4971 |
Publisher: | American Society of Hematology |
Volume: | 111 |
Number: | 1 |
Page Range: | 142-149 |
Date: | 1 January 2008 |
Official Publication: | https://doi.org/10.1182/blood-2007-07-102558 |
PubMed: | View item in PubMed |
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