4.8 Article

Endothelial podosome rosettes regulate vascular branching in tumour angiogenesis

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NATURE CELL BIOLOGY
卷 16, 期 10, 页码 931-941

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/ncb3036

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资金

  1. Associazione Italiana per la Ricerca sul Cancro (AIRC) [10133, 14635, 13016, 13604, 15026]
  2. AIRC 5x1000 [12182]
  3. Converging Technologies Program, grant: 'Photonic Biosensors for Early Cancer Diagnostics'
  4. Technological Platforms for Biotechnology: grant DRUIDI
  5. Fondazione Cassa di Risparmio Torino (CRT)
  6. Fondazione Piemontese per la Ricerca sul Cancro-ONLUS
  7. Fondo Investimenti per la Ricerca di Base [RBAP11BYNP]
  8. University of Torino-Compagnia di San Paolo: RETHE grant
  9. GeneRNet grant
  10. NIH HHS/United States [P01 CA080124/CA/NCI]
  11. Fondazione T. & L. de Beaumont Bonelli
  12. Girardi Family

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The mechanism by which angiogenic endothelial cells break the physical barrier of the vascular basement membrane and consequently sprout to form new vessels in mature tissues is unclear. Here, we show that the angiogenic endothelium is characterized by the presence of functional podosome rosettes. These extracellular-matrix-degrading and adhesive structures are precursors of de novo branching points and represent a key feature in the formation of new blood vessels. VEGF-A stimulation induces the formation of endothelial podosome rosettes by upregulating integrin alpha(6)beta(1). In contrast, the binding of alpha(6)beta(1) integrin to the laminin of the vascular basement membrane impairs the formation of podosome rosettes by restricting alpha(6)beta(1) integrin to focal adhesions and hampering its translocation to podosomes. Using an ex vivo sprouting angiogenesis assay, transgenic and knockout mouse models and human tumour sample analysis, we provide evidence that endothelial podosome rosettes control blood vessel branching and are critical regulators of pathological angiogenesis.

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