Blood · 2012
LRF-mediated Dll4 repression in erythroblasts is necessary for hematopoietic stem cell maintenance.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Lee Sung-Uk, Maeda Manami, Ishikawa Yuichi, Li Sierra Min, Wilson Anne, Jubb Adrian M, Sakurai Nagisa, Weng Lihong, Fiorini Emma, Radtke Freddy, Yan Minhong, Macdonald H Robson, Chen Ching-Cheng, Maeda Takahiro
Аннотация
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.
Предметные рубрики MeSH
Adaptor Proteins, Signal TransducingAnimalsBone Marrow CellsBone Marrow TransplantationCalcium-Binding ProteinsCell DifferentiationCell ProliferationCellular MicroenvironmentDNA-Binding ProteinsErythroblastsHematopoietic Stem CellsImmunohistochemistryIntracellular Signaling Peptides and ProteinsMembrane ProteinsMiceMice, Inbred C57BLMice, KnockoutOligonucleotide Array Sequence AnalysisReceptor, Notch1Reverse Transcriptase Polymerase Chain ReactionSignal TransductionT-LymphocytesTime FactorsTranscription FactorsTranscriptome