Zjablovskaja Polina, Kardosova Miroslava, Danek Petr, Angelisova Pavla, Benoukraf Touati, Wurm Alexander A, Kalina Tomas, Sian Stephanie, Balastik Martin, Delwel Ruud, Brdicka Tomas, Tenen Daniel G, Behre Gerhard, Fiore Fréderic, Malissen Bernard, Horejsi Vaclav, Alberich-Jorda Meritxell
Department of Hemato-oncology, Institute of Molecular Genetics of the ASCR, Videnska 1083, Prague 142 20 Prague 4, Czech Republic.
Childhood Leukaemia Investigation Prague, Department of Paediatric Haematology and Oncology, 2nd Faculty of Medicine, Charles University in Prague, University Hospital Motol, V Uvalu 84, Praha 150 06, Czech Republic.
Cell Death Differ. 2017 Apr;24(4):705-716. doi: 10.1038/cdd.2017.6. Epub 2017 Feb 10.
Development of hematopoietic populations through the process of differentiation is critical for proper hematopoiesis. The transcription factor CCAAT/enhancer binding protein alpha (C/EBPα) is a master regulator of myeloid differentiation, and the identification of C/EBPα target genes is key to understand this process. Here we identified the Ecotropic Viral Integration Site 2B (EVI2B) gene as a direct target of C/EBPα. We showed that the product of the gene, the transmembrane glycoprotein EVI2B (CD361), is abundantly expressed on the surface of primary hematopoietic cells, the highest levels of expression being reached in mature granulocytes. Using shRNA-mediated downregulation of EVI2B in human and murine cell lines and in primary hematopoietic stem and progenitor cells, we demonstrated impaired myeloid lineage development and altered progenitor functions in EVI2B-silenced cells. We showed that the compromised progenitor functionality in Evi2b-depleted cells can be in part explained by deregulation of cell proliferation and apoptosis. In addition, we generated an Evi2b knockout murine model and demonstrated altered properties of hematopoietic progenitors, as well as impaired G-CSF dependent myeloid colony formation in the knockout cells. Remarkably, we found that EVI2B is significantly downregulated in human acute myeloid leukemia samples characterized by defects in CEBPA. Altogether, our data demonstrate that EVI2B is a downstream target of C/EBPα, which regulates myeloid differentiation and functionality of hematopoietic progenitors.
通过分化过程产生造血细胞群体对于正常的造血作用至关重要。转录因子CCAAT/增强子结合蛋白α(C/EBPα)是髓系分化的主要调节因子,鉴定C/EBPα靶基因是理解这一过程的关键。在此,我们鉴定出嗜异性病毒整合位点2B(EVI2B)基因是C/EBPα的直接靶标。我们发现该基因的产物,即跨膜糖蛋白EVI2B(CD361),在原代造血细胞表面大量表达,在成熟粒细胞中表达水平最高。利用shRNA介导的方法在人和小鼠细胞系以及原代造血干细胞和祖细胞中下调EVI2B,我们证明在EVI2B沉默的细胞中髓系谱系发育受损且祖细胞功能改变。我们表明,Evi2b缺失细胞中祖细胞功能受损部分可由细胞增殖和凋亡的失调来解释。此外,我们构建了一个Evi2b基因敲除小鼠模型,并证明造血祖细胞的特性发生改变,以及敲除细胞中G-CSF依赖性髓系集落形成受损。值得注意的是,我们发现EVI2B在以CEBPA缺陷为特征的人类急性髓系白血病样本中显著下调。总之,我们的数据表明EVI2B是C/EBPα的下游靶标,其调节造血祖细胞的髓系分化和功能。