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Mechanically activated piezo channels modulate outflow tract valve development through the Yap1 and Klf2-Notch signaling axis

机译:机械激活的压电通道通过Yap1和Klf2-Notch信号轴调节流出管道阀的发展

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摘要

Mechanical forces are well known for modulating heart valve developmental programs. Yet, it is still unclear how genetic programs and mechanosensation interact during heart valve development. Here, we assessed the mechanosensitive pathways involved during zebrafish outflow tract (OFT) valve development in vivo. Our results show that the hippo effector Yap1, Klf2, and the Notch signaling pathway are all essential for OFT valve morphogenesis in response to mechanical forces, albeit active in different cell layers. Furthermore, we show that Piezo and TRP mechanosensitive channels are important factors modulating these pathways. In addition, live reporters reveal that Piezo controls Klf2 and Notch activity in the endothelium and Yap1 localization in the smooth muscle progenitors to coordinate OFT valve morphogenesis. Together, this work identifies a unique morphogenetic program during OFT valve formation and places Piezo as a central modulator of the cell response to forces in this process.
机译:机械力对于调节心脏瓣膜发育程序是众所周知的。然而,仍不清楚在心脏瓣膜发育过程中遗传程序和机械感觉如何相互作用。在这里,我们评估了体内斑马鱼流出道(OFT)瓣膜发育过程中涉及的机械敏感途径。我们的研究结果表明,河马效应因子Yap1,Klf2和Notch信号通路对于响应机械力的OFT阀形态发生都是必不可少的,尽管它们活跃于不同的细胞层。此外,我们表明压电和TRP机械敏感通道是调节这些途径的重要因素。此外,现场报道还显示,Piezo控制内皮中的Klf2和Notch活性以及平滑肌祖细胞中Yap1的定位,以协调OFT阀的形态发生。总之,这项工作确定了OFT瓣膜形成过程中独特的形态发生程序,并将压电作为该过程中细胞对力响应的中央调节器。

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