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Specific fibroblast subpopulations and neuronal structures provide local sources of Vegfc-processing components during zebrafish lymphangiogenesis

Author

Listed:
  • Guangxia Wang

    (Institute for Cardiovascular Organogenesis and Regeneration, WWU Münster
    Faculty of Medicine, WWU Münster
    Cells-in-Motion Cluster of Excellence, WWU Münster)

  • Lars Muhl

    (Karolinska Institutet)

  • Yvonne Padberg

    (Institute for Cardiovascular Organogenesis and Regeneration, WWU Münster
    Faculty of Medicine, WWU Münster
    Cells-in-Motion Cluster of Excellence, WWU Münster)

  • Laura Dupont

    (GIGA, University of Liège)

  • Josi Peterson-Maduro

    (Hubrecht Institute–KNAW & UMC Utrecht)

  • Martin Stehling

    (Flow Cytometry Unit, Max Planck Institute for Molecular Biomedicine)

  • Ferdinand Noble

    (Zoological Institute and Institute of Biological and Chemical Systems, Karlsruhe Institute of Technology (KIT)
    Institute of Experimental Cardiology, University of Heidelberg
    DZHK (German Center for Cardiovascular Research) partner site)

  • Alain Colige

    (GIGA, University of Liège)

  • Christer Betsholtz

    (Karolinska Institutet
    Rudbeck Laboratory, Uppsala University)

  • Stefan Schulte-Merker

    (Institute for Cardiovascular Organogenesis and Regeneration, WWU Münster
    Faculty of Medicine, WWU Münster
    Cells-in-Motion Cluster of Excellence, WWU Münster)

  • Andreas Impel

    (Institute for Cardiovascular Organogenesis and Regeneration, WWU Münster
    Faculty of Medicine, WWU Münster
    Cells-in-Motion Cluster of Excellence, WWU Münster)

Abstract

Proteolytical processing of the growth factor VEGFC through the concerted activity of CCBE1 and ADAMTS3 is required for lymphatic development to occur. How these factors act together in time and space, and which cell types produce these factors is not understood. Here we assess the function of Adamts3 and the related protease Adamts14 during zebrafish lymphangiogenesis and show both proteins to be able to process Vegfc. Only the simultaneous loss of both protein functions results in lymphatic defects identical to vegfc loss-of-function situations. Cell transplantation experiments demonstrate neuronal structures and/or fibroblasts to constitute cellular sources not only for both proteases but also for Ccbe1 and Vegfc. We further show that this locally restricted Vegfc maturation is needed to trigger normal lymphatic sprouting and directional migration. Our data provide a single-cell resolution model for establishing secretion and processing hubs for Vegfc during developmental lymphangiogenesis.

Suggested Citation

  • Guangxia Wang & Lars Muhl & Yvonne Padberg & Laura Dupont & Josi Peterson-Maduro & Martin Stehling & Ferdinand Noble & Alain Colige & Christer Betsholtz & Stefan Schulte-Merker & Andreas Impel, 2020. "Specific fibroblast subpopulations and neuronal structures provide local sources of Vegfc-processing components during zebrafish lymphangiogenesis," Nature Communications, Nature, vol. 11(1), pages 1-21, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-16552-7
    DOI: 10.1038/s41467-020-16552-7
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