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Neural cells play an inhibitory role in pancreatic differentiation of pluripotent stem cells

机译:神经细胞在多能干细胞的胰腺分化中起抑制作用

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摘要

Pancreatic endocrine beta-cells derived from embryonic stem (ES) cells and induced pluripotent stem (iPS) cells have received attention as screening systems for therapeutic drugs and as the basis for cell-based therapies. Here, we used a 12-day beta-cell differentiation protocol for mouse ES cells and obtained several hit compounds that promoted beta-cell differentiation. One of these compounds, mycophenolic acid (MPA), effectively promoted ES cell differentiation with a concomitant reduction of neuronal cells. The existence of neural cell-derived inhibitory humoral factors for beta-cell differentiation was suggested using a co-culture system. Based on gene array analysis, we focused on the Wnt/ beta-catenin pathway and showed that the Wnt pathway inhibitor reversed MPA-induced beta-cell differentiation. Wnt pathway activation promoted beta-cell differentiation also in human iPS cells. Our results showed that Wnt signaling activation positively regulates beta-cell differentiation, and represent a downstream target of the neural inhibitory factor.
机译:源自胚胎干(ES)细胞和诱导性多能干(iPS)细胞的胰腺内分泌β细胞已作为治疗药物的筛选系统和基于细胞疗法的基础受到关注。在这里,我们对小鼠ES细胞使用了为期12天的β细胞分化方案,并获得了几种促进β细胞分化的命中化合物。这些化合物之一,霉酚酸(MPA)可有效促进ES细胞分化,并伴随神经细胞的减少。有人建议使用共培养系统来存在神经细胞源性抑制性体液因子来促进β细胞的分化。基于基因阵列分析,我们专注于Wnt /β-catenin途径,并显示Wnt途径抑制剂逆转了MPA诱导的β细胞分化。 Wnt途径激活也促进了人类iPS细胞中的β细胞分化。我们的结果表明,Wnt信号激活正调控β细胞分化,并代表神经抑制因子的下游目标。

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