Bouilloux Fabrice, Juban Gaëtan, Cohet Nathalie, Buet Dorothée, Guyot Boris, Vainchenker William, Louache Fawzia, Morlé François
Université de Lyon, Lyon, France.
Blood. 2008 Aug 1;112(3):576-84. doi: 10.1182/blood-2007-07-098996. Epub 2008 Jun 3.
Previous observations suggested that functional antagonism between FLI-1 and EKLF might be involved in the commitment toward erythrocytic or megakaryocytic differentiation. We show here, using inducible shRNA expression, that EKLF knockdown in mouse erythroleukemia (MEL) cells decreases erythrocytic and increases megakaryocytic as well as Fli-1 gene expression. Chromatin immunoprecipitation analyses revealed that the increase in megakaryocytic gene expression is associated with a marked increase in RNA pol II and FLI-1 occupancy at their promoters, albeit FLI-1 protein levels are only minimally affected. Similarly, we show that human CD34(+) progenitors infected with shRNA lentivirus allowing EKLF knockdown generate an increased number of differentiated megakaryocytic cells associated with increased levels of megakaryocytic and Fli-1 gene transcripts. Single-cell progeny analysis of a cell population enriched in bipotent progenitors revealed that EKLF knockdown increases the number of megakaryocytic at the expense of erythrocytic colonies. Taken together, these data indicate that EKLF restricts megakaryocytic differentiation to the benefit of erythrocytic differentiation and suggest that this might be at least partially mediated by the inhibition of FLI-1 recruitment to megakaryocytic and Fli-1 gene promoters.
先前的观察结果表明,FLI-1和EKLF之间的功能拮抗作用可能参与了红细胞或巨核细胞分化的定向过程。我们在此表明,利用可诱导的shRNA表达,在小鼠红白血病(MEL)细胞中敲低EKLF会降低红细胞生成,增加巨核细胞生成以及Fli-1基因表达。染色质免疫沉淀分析显示,巨核细胞基因表达的增加与RNA聚合酶II和FLI-1在其启动子上的占据显著增加相关,尽管FLI-1蛋白水平仅受到最小程度的影响。同样,我们表明,感染允许敲低EKLF的shRNA慢病毒的人CD34(+)祖细胞会产生更多分化的巨核细胞,这与巨核细胞和Fli-1基因转录本水平的增加相关。对富含双能祖细胞的细胞群体进行单细胞后代分析表明,敲低EKLF会以红细胞集落为代价增加巨核细胞的数量。综上所述,这些数据表明EKLF限制巨核细胞分化以利于红细胞分化,并表明这可能至少部分是由抑制FLI-1募集到巨核细胞和Fli-1基因启动子介导的。