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Notch-dependent VEGFR3 upregulation allows angiogenesis without VEGF–VEGFR2 signalling

Author

Listed:
  • Rui Benedito

    (Max Planck Institute for Molecular Biomedicine, D-48149 Münster, Germany
    University of Münster, Faculty of Medicine, D-48149 Münster, Germany)

  • Susana F. Rocha

    (Max Planck Institute for Molecular Biomedicine, D-48149 Münster, Germany
    University of Münster, Faculty of Medicine, D-48149 Münster, Germany)

  • Marina Woeste

    (Max Planck Institute for Molecular Biomedicine, D-48149 Münster, Germany
    University of Münster, Faculty of Medicine, D-48149 Münster, Germany)

  • Martin Zamykal

    (Max Planck Institute for Molecular Biomedicine, D-48149 Münster, Germany
    University of Münster, Faculty of Medicine, D-48149 Münster, Germany)

  • Freddy Radtke

    (Ecole Polytechnique Fédérale de Lausanne (EPFL), Swiss Institute for Experimental Cancer Research (ISREC), CH-1015 Lausanne, Switzerland)

  • Oriol Casanovas

    (Translational Research Laboratory, Catalan Institute of Oncology, IDIBELL, 08907 L’Hospitalet de Llobregat, Spain)

  • Antonio Duarte

    (The Interdisciplinary Centre of Research in Animal Health (CIISA), Faculty of Veterinary Medicine, Technical University of Lisbon, 1300-474 Lisbon, Portugal)

  • Bronislaw Pytowski

    (ImClone Systems, 180 Varick Street)

  • Ralf H. Adams

    (Max Planck Institute for Molecular Biomedicine, D-48149 Münster, Germany
    University of Münster, Faculty of Medicine, D-48149 Münster, Germany)

Abstract

DLL4–Notch signalling suppresses endothelial sprouting and angiogenic growth through crosstalk with the vascular endothelial growth factor (VEGF) pathway; VEGF receptor 2 has been thought to have a crucial role in this crosstalk, but now VEGF receptor 3 is shown to be the more important modulator.

Suggested Citation

  • Rui Benedito & Susana F. Rocha & Marina Woeste & Martin Zamykal & Freddy Radtke & Oriol Casanovas & Antonio Duarte & Bronislaw Pytowski & Ralf H. Adams, 2012. "Notch-dependent VEGFR3 upregulation allows angiogenesis without VEGF–VEGFR2 signalling," Nature, Nature, vol. 484(7392), pages 110-114, April.
  • Handle: RePEc:nat:nature:v:484:y:2012:i:7392:d:10.1038_nature10908
    DOI: 10.1038/nature10908
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    Cited by:

    1. Fuchun Yang & Shiva Kalantari & Banzhan Ruan & Shaogang Sun & Zhaoqun Bian & Jun-Lin Guan, 2023. "Autophagy inhibition prevents lymphatic malformation progression to lymphangiosarcoma by decreasing osteopontin and Stat3 signaling," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    2. Jeremiah Bernier-Latmani & Cristina Mauri & Rachel Marcone & François Renevey & Stephan Durot & Liqun He & Michael Vanlandewijck & Catherine Maclachlan & Suzel Davanture & Nicola Zamboni & Graham W. K, 2022. "ADAMTS18+ villus tip telocytes maintain a polarized VEGFA signaling domain and fenestrations in nutrient-absorbing intestinal blood vessels," Nature Communications, Nature, vol. 13(1), pages 1-17, December.

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