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首页> 外文期刊>Stem Cell Reports >Unraveling the Inconsistencies of Cardiac Differentiation Efficiency Induced by the GSK3β Inhibitor CHIR99021 in Human Pluripotent Stem Cells
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Unraveling the Inconsistencies of Cardiac Differentiation Efficiency Induced by the GSK3β Inhibitor CHIR99021 in Human Pluripotent Stem Cells

机译:揭示人多能干细胞中GSK3β抑制剂CHIR99021诱导的心脏分化效率的不一致。

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Summary Cardiac differentiation efficiency is hampered by inconsistencies and low reproducibility. We analyzed the differentiation process of multiple human pluripotent stem cell (hPSC) lines in response to dynamic GSK3β inhibition under varying cell culture conditions. hPSCs showed strong differences in cell-cycle profiles with varying culture confluency. hPSCs with a higher percentage of cells in the G1 phase of the cell cycle exhibited cell death and required lower doses of GSK3β inhibitors to induce cardiac differentiation. GSK3β inhibition initiated cell-cycle progression via cyclin D1 and modulated both Wnt signaling and the transcription factor (TCF) levels, resulting in accelerated or delayed mesoderm differentiation. The TCF levels were key regulators during hPSC differentiation with CHIR99021. Our results explain how differences in hPSC lines and culture conditions impact cell death and cardiac differentiation. By analyzing the cell cycle, we were able to select for highly cardiogenic hPSC lines and increase the experimental reproducibility by predicting differentiation outcomes.
机译:总结不一致和低重复性阻碍了心脏分化效率。我们分析了在变化的细胞培养条件下响应动态GSK3β抑制的多个人多能干细胞(hPSC)系的分化过程。 hPSC在不同的培养融合度下显示出细胞周期概况的强烈差异。在细胞周期G1期中具有较高百分比细胞的hPSC表现出细胞死亡,并需要较低剂量的GSK3β抑制剂来诱导心脏分化。 GSK3β抑制通过细胞周期蛋白D1启动细胞周期进程,并调节Wnt信号传导和转录因子(TCF)水平,从而导致中胚层分化加速或延迟。在用CHIR99021进行hPSC分化期间,TCF水平是关键的调节因子。我们的结果解释了hPSC品系和培养条件的差异如何影响细胞死亡和心脏分化。通过分析细胞周期,我们能够选择高心源性hPSC品系,并通过预测分化结果来提高实验可重复性。

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