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

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Abstract
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.
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Funding Information
  • H2020 European Research Council (682938 - EVALVE)
  • Fondation pour la Recherche Médicale (DEQ29553)
  • Agence Nationale de la Recherche (ANR-15-CE13-0015-01)
  • European Molecular Biology Organization (Young Investigator Program)
  • Fondation Lefoulon Delalande
  • Agence Nationale de la Recherche (ANR-10-IDEX-0002-02)
  • Agence Nationale de la Recherche (ANR-12-ISV2-0001-01)
  • Agence Nationale de la Recherche (ANR-10-LABX-0030-INRT)

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