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


Autoria(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.
Data(s)

2013

Resumo

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.

Identificador

http://serval.unil.ch/?id=serval:BIB_7FF8C49D4568

isbn:1528-0020 (Electronic)

pmid:23134786

doi:10.1182/blood-2012-03-418103

isiid:000314868800013

Idioma(s)

en

Fonte

Blood, vol. 121, no. 6, pp. 918-929

Palavras-Chave #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
Tipo

info:eu-repo/semantics/article

article