Jagged1-dependent Notch signaling is dispensable for hematopoietic stem cell self-renewal and differentiation
Jagged1-mediated Notch signaling has been suggested to be critically involved in hematopoietic stem cell (HSC) self-renewal. Unexpectedly, we report here that inducible Cre-loxP-mediated inactivation of the Jagged1 gene in bone marrow progenitors and/or bone marrow (BM) stromal cells does not impair HSC self-renewal or differentiation in all blood lineages. Mice with simultaneous inactivation of Jagged1 and Notch1 in the BM compartment survived normally following a 5FU-based in vivo challenge. In addition, Notch1-deficient HSCs were able to reconstitute mice with inactivated Jagged1 in the BM stroma even under competitive conditions. In contrast to earlier reports, these data exclude an essential role for Jagged1-mediated Notch signaling during hematopoiesis.
- URL: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=15550486
Keywords: Animals ; Antimetabolites/administration & dosage/toxicity ; Bone Marrow/physiology ; Calcium-Binding Proteins/deficiency/*metabolism ; Cell Differentiation/drug effects/*physiology ; *Cell Proliferation ; Fluorouracil/administration & dosage/toxicity ; Hematopoiesis/drug effects/physiology ; Hematopoietic Stem Cells/cytology/*physiology ; Integrases/genetics ; Membrane Proteins/deficiency/*metabolism ; Mice ; Mice ; Transgenic ; Receptors ; Notch/deficiency/*metabolism ; Research Support ; Non-U.S. Gov't ; Signal Transduction/drug effects/*physiology ; Stromal Cells/cytology/physiology ; Viral Proteins/genetics
Ludwig Institute for Cancer Research, Lausanne Branch, University of Lausanne, 1066 Epalinges, Switzerland.
Record created on 2006-12-05, modified on 2016-08-08