Won Haejung, Nandakumar Vijayalakshmi, Yates Peter, Sanchez Suzi, Jones Lindsey, Huang Xue F, Chen Si-Yi
Department of Molecular Microbiology and Immunology, Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA.
Blood. 2014 Oct 23;124(17):2647-56. doi: 10.1182/blood-2013-10-534313. Epub 2014 Sep 12.
The mechanisms controlling the development of dendritic cells (DCs) remain incompletely understood. Using an Mysm1 knockout (Mysm1(-/-)) mouse model, we identified the histone H2A deubiquitinase Mysm1, as a critical regulator in DC differentiation. Mysm1(-/-) mice showed a global reduction of DCs in lymphoid organs, whereas development of granulocytes and macrophages were not severely affected. Hematopoietic progenitors and DC precursors were significantly decreased in Mysm1(-/-) mice and defective in Fms-like tyrosine kinase-3(Flt3) ligand-induced, but not in granulocyte macrophage-colony-stimulating factor (GM-CSF)-induced DC differentiation in vitro. Molecular studies demonstrated that the developmental defect of DCs from common myeloid progenitor (CMP) in Mysm1(-/-) mice is associated with decreased Flt3 expression and that Mysm1 derepresses transcription of the Flt3 gene by directing histone modifications at the Flt3 promoter region. Two molecular mechanisms were found to be responsible for the selective role of Mysm1 in lineage determination of DCs from CMPs: the selective expression of Mysm1 in a subset of CMPs and the different requirement of Mysm1 for PU.1 recruitment to the Flt3 locus vs GM-CSF-α and macrophage-colony-stimulating factor receptor loci. In conclusion, this study reveals an essential role of Mysm1 in epigenetic regulation of Flt3 transcription and DC development, and it provides a novel mechanism for lineage determination from CMP.
控制树突状细胞(DCs)发育的机制仍未完全明确。利用Mysm1基因敲除(Mysm1(-/-))小鼠模型,我们确定组蛋白H2A去泛素化酶Mysm1是DC分化的关键调节因子。Mysm1(-/-)小鼠的淋巴器官中DCs整体减少,而粒细胞和巨噬细胞的发育未受到严重影响。Mysm1(-/-)小鼠的造血祖细胞和DC前体显著减少,在体外对Fms样酪氨酸激酶-3(Flt3)配体诱导的DC分化有缺陷,但对粒细胞巨噬细胞集落刺激因子(GM-CSF)诱导的DC分化无缺陷。分子研究表明,Mysm1(-/-)小鼠中来自常见髓系祖细胞(CMP)的DCs发育缺陷与Flt3表达降低有关,并且Mysm1通过在Flt3启动子区域引导组蛋白修饰来解除对Flt3基因转录的抑制。发现两种分子机制负责Mysm1在CMPs向DCs谱系决定中的选择性作用:Mysm1在一部分CMPs中的选择性表达以及Mysm1对PU.1募集到Flt3基因座与GM-CSF-α和巨噬细胞集落刺激因子受体基因座的不同需求。总之,本研究揭示了Mysm1在Flt3转录和DC发育的表观遗传调控中的重要作用,并为CMP的谱系决定提供了一种新机制。