VEGFR1 (Flt1) regulates Rab4 recycling to control fibronectin polymerization and endothelial vessel branching

Matthew C. Jones, Patrick T. Caswell, Kim Moran-Jones, Marnie Roberts, Simon T. Barry, Alexandra Gampel, Harry Mellor, Jim C. Norman

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The cell's main receptor for VEGF, VEGFR2 (Kdr) is one of the most important positive regulators of new blood vessel growth and its downstream signalling is well characterized. By contrast, VEGFR1 (Flt1) and the mechanisms by which this VEGF receptor promotes branching morphogenesis in angiogenesis remain relatively unclear. Here we report that engagement of VEGFR1 activates a Rab4A-dependent pathway that transports αvβ3 integrin from early endosomes to the plasma membrane, and that this is required for VEGF-driven fibronectin polymerization in endothelial cells. Furthermore, VEGFR1 acts to promote endothelial tubule branching in an organotypic model of angiogenesis via a mechanism that requires Rab4A and αvβ3 integrin. We conclude that a recycling pathway regulated by Rab4A is a critical effector of VEGFR1 during branching morphogenesis of the vasculature. © 2009 The Authors Journal compilation © 2009 Blackwell Munksgaard.
    Original languageEnglish
    Pages (from-to)754-766
    Number of pages12
    JournalTraffic (Malden): the international journal of intracellular transport
    Volume10
    Issue number6
    DOIs
    Publication statusPublished - 2009

    Keywords

    • Angiogenesis
    • Branching morphogenesis
    • Endocytosis
    • Fibronectin integrin
    • PlGF
    • Polymerization
    • Rab4
    • Recycling
    • VEGF
    • VEGFR1 (Flt1)
    • VEGFR2 (Kdr)

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