Eliades Alexia, Papadantonakis Nikolaos, Ravid Katya
Department of Medicine and Biochemistry, Evans Center for Interdisciplinary Biomedical Research, Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, Massachusetts 02118, USA.
J Biol Chem. 2010 Jun 11;285(24):18909-17. doi: 10.1074/jbc.M110.102145. Epub 2010 Apr 14.
Megakaryocytes are platelet precursor cells that undergo endomitosis. During this process, repeated rounds of DNA synthesis are characterized by lack of late anaphase and cytokinesis. Physiologically, the majority of the polyploid megakaryocytes in the bone marrow are cell cycle arrested. As previously reported, cyclin E is essential for megakaryocyte polyploidy; however, it has remained unclear whether up-regulated cyclin E is an inducer of polyploidy in vivo. We found that cyclin E is up-regulated upon stimulation of primary megakaryocytes by thrombopoietin. Transgenic mice in which elevated cyclin E expression is targeted to megakaryocytes display an increased ploidy profile. Examination of S phase markers, specifically proliferating cell nuclear antigen, cyclin A, and 5-bromo-2-deoxyuridine reveals that cyclin E promotes progression to S phase and cell cycling. Interestingly, analysis of Cdc6 and Mcm2 indicates that cyclin E mediates its effect by promoting the expression of components of the pre-replication complex. Furthermore, we show that up-regulated cyclin E results in the up-regulation of cyclin B1 levels, suggesting an additional mechanism of cyclin E-mediated ploidy increase. These findings define a key role for cyclin E in promoting megakaryocyte entry into S phase and hence, increase in the number of cell cycling cells and in augmenting polyploidization.
巨核细胞是经历核内有丝分裂的血小板前体细胞。在此过程中,DNA合成的重复轮次的特征是缺乏后期和胞质分裂。在生理状态下,骨髓中大多数多倍体巨核细胞处于细胞周期停滞状态。如先前报道,细胞周期蛋白E对巨核细胞多倍体化至关重要;然而,尚不清楚上调的细胞周期蛋白E在体内是否是多倍体化的诱导剂。我们发现,血小板生成素刺激原代巨核细胞后,细胞周期蛋白E会上调。细胞周期蛋白E表达升高靶向巨核细胞的转基因小鼠显示出多倍体谱增加。对S期标志物,特别是增殖细胞核抗原、细胞周期蛋白A和5-溴-2-脱氧尿苷的检测表明,细胞周期蛋白E促进细胞进入S期和细胞循环。有趣的是,对Cdc6和Mcm2的分析表明,细胞周期蛋白E通过促进复制前复合体成分的表达来介导其作用。此外,我们表明上调的细胞周期蛋白E导致细胞周期蛋白B1水平上调,提示细胞周期蛋白E介导的多倍体增加的另一种机制。这些发现确定了细胞周期蛋白E在促进巨核细胞进入S期从而增加细胞循环细胞数量和增强多倍体化方面的关键作用。