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Notch1 信号通路通过 Sox9 的激活调控软骨细胞谱系的确定。

Notch1 signaling regulates chondrogenic lineage determination through Sox9 activation.

机构信息

Department of Virology and Cell Biology, University of Lübeck, Ratzeburger Allee 160, Lübeck, Germany.

出版信息

Cell Death Differ. 2012 Mar;19(3):461-9. doi: 10.1038/cdd.2011.114. Epub 2011 Aug 26.

Abstract

Notch signaling is involved in several cell lineage determination processes during embryonic development. Recently, we have shown that Sox9 is most likely a primary target gene of Notch1 signaling in embryonic stem cells (ESCs). By using our in vitro differentiation protocol for chondrogenesis from ESCs through embryoid bodies (EBs) together with our tamoxifen-inducible system to activate Notch1, we analyzed the function of Notch signaling and its induction of Sox9 during EB differentiation towards the chondrogenic lineage. Temporary activation of Notch1 during early stages of EB, when lineage determination occurs, was accompanied by rapid and transient Sox9 upregulation and resulted in induction of chondrogenic differentiation during later stages of EB cultivation. Using siRNA targeting Sox9, we knocked down and adjusted this early Notch1-induced Sox9 expression peak to non-induced levels, which led to reversion of Notch1-induced chondrogenic differentiation. In contrast, continuous Notch1 activation during EB cultivation resulted in complete inhibition of chondrogenic differentiation. Furthermore, a reduction and delay of cardiac differentiation observed in EBs after early Notch1 activation was not reversed by siRNA-mediated Sox9 knockdown. Our data indicate that Notch1 signaling has an important role during early stages of chondrogenic lineage determination by regulation of Sox9 expression.

摘要

Notch 信号通路参与胚胎发育过程中的几个细胞谱系决定过程。最近,我们已经表明 Sox9 很可能是胚胎干细胞(ESCs)中 Notch1 信号通路的主要靶基因。通过使用我们的从 ESCs 通过胚状体(EBs)体外分化为软骨的方案,以及我们的他莫昔芬诱导的 Notch1 激活系统,我们分析了 Notch 信号通路及其在 EB 向软骨谱系分化过程中诱导 Sox9 的功能。在 EB 发生谱系决定的早期阶段,短暂激活 Notch1 伴随着 Sox9 的快速和短暂上调,并导致 EB 培养后期的软骨分化诱导。使用靶向 Sox9 的 siRNA,我们敲低并将这种早期 Notch1 诱导的 Sox9 表达峰调整到未诱导水平,这导致 Notch1 诱导的软骨分化发生逆转。相比之下,在 EB 培养过程中持续激活 Notch1 会导致完全抑制软骨分化。此外,在早期 Notch1 激活后,EB 中观察到的心脏分化减少和延迟,不能通过 Sox9 敲低的 siRNA 逆转。我们的数据表明,Notch1 信号通路通过调节 Sox9 的表达在软骨谱系决定的早期阶段发挥重要作用。

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本文引用的文献

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The Notch signaling pathway: molecular basis of cell context dependency.Notch 信号通路:细胞上下文相关性的分子基础。
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