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首页> 外文期刊>Development >beta-catenin/TCF/Lef controls a differentiation-associated transcriptional program in renal epithelial progenitors.
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beta-catenin/TCF/Lef controls a differentiation-associated transcriptional program in renal epithelial progenitors.

机译:β-catenin/ TCF / Lef控制着肾上皮祖细胞的分化相关转录程序。

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In the embryonic kidney, progenitors in the metanephric mesenchyme differentiate into specialized renal epithelia in a defined sequence characterized by the formation of cellular aggregates, conversion into polarized epithelia and segmentation along a proximal-distal axis. This sequence is reiterated throughout renal development to generate nephrons. Here, we identify global transcriptional programs associated with epithelial differentiation utilizing an organ culture model of rat metanephric mesenchymal differentiation, which recapitulates the hallmarks of epithelialization in vivo in a synchronized rather than reiterative fashion. We observe activation of multiple putative targets of beta-catenin/TCF/Lef-dependent transcription coinciding with epithelial differentiation. We show in cultured explants that isolated activation of beta-catenin signaling in epithelial progenitors induces, in a TCF/Lef-dependent manner, a subset of the transcripts associated with epithelialization, including Pax8, cyclin D1 (Ccnd1) and Emx2. This is associated with anti-apoptotic and proliferative effects in epithelial progenitors, whereas cells with impaired TCF/Lef-dependent transcription are progressively depleted from the epithelial lineage. In vivo, TCF/Lef-responsive genes comprise a conserved transcriptional program in differentiating renal epithelial progenitors and beta-catenin-containing transcriptional complexes directly bind to their promoter regions. Thus, beta-catenin/TCF/Lef-mediated transcriptional events control a subset of the differentiation-associated transcriptional program and thereby participate in maintenance, expansion and stage progression of the epithelial lineage.
机译:在胚胎肾脏中,后肾间充质的祖细胞以确定的序列分化为专门的肾上皮细胞,其特征是形成细胞聚集体,转化为极化的上皮细胞并沿近端-远端轴分割。在整个肾脏发育过程中重申该序列以产生肾单位。在这里,我们使用大鼠后肾间充质分化的器官培养模型,确定与上皮分化相关的全球转录程序,该模型以同步而非重复的方式概括了体内上皮化的标志。我们观察到β-catenin/ TCF / Lef依赖性转录的多个推定靶标的激活与上皮分化一致。我们在培养的外植体中显示,上皮祖细胞中β-catenin信号的分离激活以TCF / Lef依赖性方式诱导与上皮化相关的转录子的子集,包括Pax8,cyclin D1(Ccnd1)和Emx2。这与上皮祖细胞的抗凋亡和增殖作用有关,而TCF / Lef依赖性转录受损的细胞则从上皮细胞系中逐渐消耗。在体内,TCF / Lef反应性基因在区分肾上皮祖细胞方面包含保守的转录程序,而含β-catenin的转录复合物直接与其启动子区域结合。因此,β-连环蛋白/ TCF / Lef介导的转录事件控制着分化相关转录程序的一个子集,从而参与了上皮谱系的维持,扩展和阶段发展。

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