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Multiple pkd and piezo gene family members are required for atrioventricular valve formation

Author

Listed:
  • Thomas Juan

    (Max Planck Institute for Heart and Lung Research, Department of Developmental Genetics
    German Centre for Cardiovascular Research (DZHK), Partner Site Rhine-Main
    Cardio-Pulmonary Institute (CPI))

  • Agatha Ribeiro da Silva

    (Max Planck Institute for Heart and Lung Research, Department of Developmental Genetics
    German Centre for Cardiovascular Research (DZHK), Partner Site Rhine-Main)

  • Bárbara Cardoso

    (Max Planck Institute for Heart and Lung Research, Department of Developmental Genetics
    German Centre for Cardiovascular Research (DZHK), Partner Site Rhine-Main)

  • SoEun Lim

    (Max Planck Institute for Heart and Lung Research, Department of Developmental Genetics
    German Centre for Cardiovascular Research (DZHK), Partner Site Rhine-Main)

  • Violette Charteau

    (Max Planck Institute for Heart and Lung Research, Department of Developmental Genetics
    German Centre for Cardiovascular Research (DZHK), Partner Site Rhine-Main
    Radboud University)

  • Didier Y. R. Stainier

    (Max Planck Institute for Heart and Lung Research, Department of Developmental Genetics
    German Centre for Cardiovascular Research (DZHK), Partner Site Rhine-Main
    Cardio-Pulmonary Institute (CPI))

Abstract

Cardiac valves ensure unidirectional blood flow through the heart, and altering their function can result in heart failure. Flow sensing via wall shear stress and wall stretching through the action of mechanosensors can modulate cardiac valve formation. However, the identity and precise role of the key mechanosensors and their effectors remain mostly unknown. Here, we genetically dissect the role of Pkd1a and other mechanosensors in atrioventricular (AV) valve formation in zebrafish and identify a role for several pkd and piezo gene family members in this process. We show that Pkd1a, together with Pkd2, Pkd1l1, and Piezo2a, promotes AV valve elongation and cardiac morphogenesis. Mechanistically, Pkd1a, Pkd2, and Pkd1l1 all repress the expression of klf2a and klf2b, transcription factor genes implicated in AV valve development. Furthermore, we find that the calcium-dependent protein kinase Camk2g is required downstream of Pkd function to repress klf2a expression. Altogether, these data identify, and dissect the role of, several mechanosensors required for AV valve formation, thereby broadening our understanding of cardiac valvulogenesis.

Suggested Citation

  • Thomas Juan & Agatha Ribeiro da Silva & Bárbara Cardoso & SoEun Lim & Violette Charteau & Didier Y. R. Stainier, 2023. "Multiple pkd and piezo gene family members are required for atrioventricular valve formation," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-35843-3
    DOI: 10.1038/s41467-023-35843-3
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    References listed on IDEAS

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    1. Emily Steed & Nathalie Faggianelli & Stéphane Roth & Caroline Ramspacher & Jean-Paul Concordet & Julien Vermot, 2016. "klf2a couples mechanotransduction and zebrafish valve morphogenesis through fibronectin synthesis," Nature Communications, Nature, vol. 7(1), pages 1-14, September.
    2. Sébastien Gauvrit & Alethia Villasenor & Boris Strilic & Philip Kitchen & Michelle M. Collins & Rubén Marín-Juez & Stefan Guenther & Hans-Martin Maischein & Nana Fukuda & Maurice A. Canham & Joshua M., 2018. "HHEX is a transcriptional regulator of the VEGFC/FLT4/PROX1 signaling axis during vascular development," Nature Communications, Nature, vol. 9(1), pages 1-14, December.
    3. Akira Muto & Pradeep Lal & Deepak Ailani & Gembu Abe & Mari Itoh & Koichi Kawakami, 2017. "Activation of the hypothalamic feeding centre upon visual prey detection," Nature Communications, Nature, vol. 8(1), pages 1-10, April.
    4. Mohamed A. El-Brolosy & Zacharias Kontarakis & Andrea Rossi & Carsten Kuenne & Stefan Günther & Nana Fukuda & Khrievono Kikhi & Giulia L. M. Boezio & Carter M. Takacs & Shih-Lei Lai & Ryuichi Fukuda &, 2019. "Genetic compensation triggered by mutant mRNA degradation," Nature, Nature, vol. 568(7751), pages 193-197, April.
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    Cited by:

    1. Sine Yaganoglu & Konstantinos Kalyviotis & Christina Vagena-Pantoula & Dörthe Jülich & Benjamin M. Gaub & Maaike Welling & Tatiana Lopes & Dariusz Lachowski & See Swee Tang & Armando Del Rio Hernandez, 2023. "Highly specific and non-invasive imaging of Piezo1-dependent activity across scales using GenEPi," Nature Communications, Nature, vol. 14(1), pages 1-16, December.

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