Arteriolar and venular patterning in retinas of mice selectively expressing VEGF isoforms.

نویسندگان

  • Ingeborg Stalmans
  • Yin-Shan Ng
  • Richard Rohan
  • Marcus Fruttiger
  • Ann Bouché
  • Ali Yuce
  • Hajime Fujisawa
  • Bart Hermans
  • Moshe Shani
  • Sandra Jansen
  • Dan Hicklin
  • David J Anderson
  • Tom Gardiner
  • Hans-Peter Hammes
  • Lieve Moons
  • Mieke Dewerchin
  • Désiré Collen
  • Peter Carmeliet
  • Patricia A D'Amore
چکیده

The murine VEGF gene is alternatively transcribed to yield the VEGF(120), VEGF(164), and VEGF(188) isoforms, which differ in their potential to bind to heparan sulfate and neuropilin-1 and to stimulate endothelial growth. Here, their role in retinal vascular development was studied in mice selectively expressing single isoforms. VEGF(164/164) mice were normal, healthy, and had normal retinal angiogenesis. In contrast, VEGF(120/120) mice exhibited severe defects in vascular outgrowth and patterning, whereas VEGF(188/188) mice displayed normal venular outgrowth but impaired arterial development. It is noteworthy that neuropilin-1, a receptor for VEGF(164), was predominantly expressed in retinal arterioles. These findings reveal distinct roles of the various VEGF isoforms in vascular patterning and arterial development in the retina.

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عنوان ژورنال:
  • The Journal of clinical investigation

دوره 109 3  شماره 

صفحات  -

تاریخ انتشار 2002