Abstract
In midgestation mouse embryos, the aorta-gonad-mesonephros (AGM) region generates hematopoietic stem cells and definitive hematopoiesis is regulated by cell-cell interaction and signaling molecules. We showed that a Ras/mitogen-activated protein (MAP) kinase signaling-specific inhibitor and a dominant negative mutant Ras blocked the production of CD45+ hematopoietic cells in embryonic day 11.5 AGM culture, indicating an essential role for the MAP kinase pathway in AGM hematopoiesis. Overexpression of the Ras/MAP kinase pathway regulator, Spred-2, in the AGM culture significantly reduced the number of CD45+ cells. In contrast, production of CD45+ cells from the AGM region of Spred-2-null mice was up-regulated as compared with wild-type littermates. Furthermore, Spred-2-deficient mice exhibited elevated hematopoietic colony formation from vascular endothelial-cadherin+ cells. These data indicate that Spred-2 functions as a negative regulator of AGM hematopoiesis by inhibiting hematopoietic cytokine signaling.
Original language | English |
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Pages (from-to) | 737-742 |
Number of pages | 6 |
Journal | Journal of Experimental Medicine |
Volume | 199 |
Issue number | 5 |
DOIs | |
Publication status | Published - 2004 Mar 1 |
Externally published | Yes |
Keywords
- AGM
- C-Kit
- Differentiation
- Hematopoiesis
- SCF
ASJC Scopus subject areas
- Medicine(all)