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Endothelial cells are progenitors of cardiac pericytes and vascular smooth muscle cells

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  • Qi Chen

    (Max Planck Institute for Molecular Biomedicine, Faculty of Medicine, University of Münster)

  • Hui Zhang

    (Key Laboratory of Nutrition and Metabolism, Institute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences)

  • Yang Liu

    (Max Planck Institute for Molecular Biomedicine, Faculty of Medicine, University of Münster)

  • Susanne Adams

    (Max Planck Institute for Molecular Biomedicine, Faculty of Medicine, University of Münster)

  • Hanna Eilken

    (Max Planck Institute for Molecular Biomedicine, Faculty of Medicine, University of Münster)

  • Martin Stehling

    (Electron Microscopy and Flow Cytometry Units, Max Planck Institute for Molecular Biomedicine)

  • Monica Corada

    (IFOM Fondazione, FIRC Institute of Molecular Oncology)

  • Elisabetta Dejana

    (IFOM Fondazione, FIRC Institute of Molecular Oncology
    University of Milan)

  • Bin Zhou

    (Key Laboratory of Nutrition and Metabolism, Institute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences)

  • Ralf H. Adams

    (Max Planck Institute for Molecular Biomedicine, Faculty of Medicine, University of Münster)

Abstract

Mural cells of the vessel wall, namely pericytes and vascular smooth muscle cells, are essential for vascular integrity. The developmental sources of these cells and molecular mechanisms controlling their progenitors in the heart are only partially understood. Here we show that endocardial endothelial cells are progenitors of pericytes and vascular smooth muscle cells in the murine embryonic heart. Endocardial cells undergo endothelial–mesenchymal transition and convert into primitive mesenchymal progenitors expressing the platelet-derived growth factor receptors, PDGFRα and PDGFRβ. These progenitors migrate into the myocardium, differentiate and assemble the wall of coronary vessels, which requires canonical Wnt signalling involving Frizzled4, β-catenin and endothelial cell-derived Wnt ligands. Our findings identify a novel and unexpected population of progenitors for coronary mural cells with potential relevance for heart function and disease conditions.

Suggested Citation

  • Qi Chen & Hui Zhang & Yang Liu & Susanne Adams & Hanna Eilken & Martin Stehling & Monica Corada & Elisabetta Dejana & Bin Zhou & Ralf H. Adams, 2016. "Endothelial cells are progenitors of cardiac pericytes and vascular smooth muscle cells," Nature Communications, Nature, vol. 7(1), pages 1-13, November.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms12422
    DOI: 10.1038/ncomms12422
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    Cited by:

    1. Jia Cao & Ling Jin & Zi-Qi Yan & Xiao-Kai Wang & You-You Li & Zun Wang & Yi-Wei Liu & Hong-Ming Li & Zhe Guan & Ze-Hui He & Jiang-Shan Gong & Jiang-Hua Liu & Hao Yin & Yi-Juan Tan & Chun-Gu Hong & Shi, 2023. "Reassessing endothelial-to-mesenchymal transition in mouse bone marrow: insights from lineage tracing models," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    2. Jong Geol Lee & Jung-Min Yon & Globinna Kim & Seul-Gi Lee & C-Yoon Kim & Seung-A Cheong & Hyun-Yi Kim & Jiyoung Yu & Kyunggon Kim & Young Hoon Sung & Hyun Ju Yoo & Dong-Cheol Woo & Jin Kyung Rho & Cha, 2024. "PIBF1 regulates trophoblast syncytialization and promotes cardiovascular development," Nature Communications, Nature, vol. 15(1), pages 1-19, December.
    3. Rachana R. Chandran & Yi Xie & Eunate Gallardo-Vara & Taylor Adams & Rolando Garcia-Milian & Inamul Kabir & Abdul Q. Sheikh & Naftali Kaminski & Kathleen A. Martin & Erica L. Herzog & Daniel M. Greif, 2021. "Distinct roles of KLF4 in mesenchymal cell subtypes during lung fibrogenesis," Nature Communications, Nature, vol. 12(1), pages 1-17, December.

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