LRF-mediated Dll4 repression in erythroblasts is necessary for hematopoietic stem cell maintenance.

Détails

ID Serval
serval:BIB_7FF8C49D4568
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
LRF-mediated Dll4 repression in erythroblasts is necessary for hematopoietic stem cell maintenance.
Périodique
Blood
Auteur(s)
Lee S.U., Maeda M., Ishikawa Y., Li S.M., Wilson A., Jubb A.M., Sakurai N., Weng L., Fiorini E., Radtke F., Yan M., Macdonald H.R., Chen C.C., Maeda T.
ISSN
1528-0020 (Electronic)
ISSN-L
0006-4971
Statut éditorial
Publié
Date de publication
2013
Volume
121
Numéro
6
Pages
918-929
Langue
anglais
Résumé
Hematopoietic stem cells (HSCs) are the most primitive cells in the hematopoietic system and are under tight regulation for self-renewal and differentiation. Notch signals are essential for the emergence of definitive hematopoiesis in mouse embryos and are critical regulators of lymphoid lineage fate determination. However, it remains unclear how Notch regulates the balance between HSC self-renewal and differentiation in the adult bone marrow (BM). Here we report a novel mechanism that prevents HSCs from undergoing premature lymphoid differentiation in BM. Using a series of in vivo mouse models and functional HSC assays, we show that leukemia/lymphoma related factor (LRF) is necessary for HSC maintenance by functioning as an erythroid-specific repressor of Delta-like 4 (Dll4) expression. Lrf deletion in erythroblasts promoted up-regulation of Dll4 in erythroblasts, sensitizing HSCs to T-cell instructive signals in the BM. Our study reveals novel cross-talk between HSCs and erythroblasts, and sheds a new light on the regulatory mechanisms regulating the balance between HSC self-renewal and differentiation.
Mots-clé
Animals, Bone Marrow Cells/metabolism, Bone Marrow Transplantation, Cell Differentiation/genetics, Cell Proliferation, Cellular Microenvironment/genetics, DNA-Binding Proteins/genetics, DNA-Binding Proteins/metabolism, Erythroblasts/metabolism, Hematopoietic Stem Cells/metabolism, Immunohistochemistry, Intracellular Signaling Peptides and Proteins/genetics, Intracellular Signaling Peptides and Proteins/metabolism, Membrane Proteins/genetics, Membrane Proteins/metabolism, Mice, Mice, Inbred C57BL, Mice, Knockout, Oligonucleotide Array Sequence Analysis, Receptor, Notch1/genetics, Receptor, Notch1/metabolism, Reverse Transcriptase Polymerase Chain Reaction, Signal Transduction/genetics, T-Lymphocytes/metabolism, Time Factors, Transcription Factors/genetics, Transcription Factors/metabolism, Transcriptome/genetics
Pubmed
Web of science
Open Access
Oui
Création de la notice
28/01/2013 9:03
Dernière modification de la notice
20/08/2019 14:40
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