4.7 Article

Vascular endothelial growth factor regulation of Weibel-Palade-body exocytosis

Journal

BLOOD
Volume 105, Issue 1, Pages 207-214

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2004-04-1519

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Funding

  1. NCRR NIH HHS [RR07002, T32 RR007002] Funding Source: Medline
  2. NHLBI NIH HHS [K08 HL074945, P01 HL65608, P01 HL056091-100003, P01 HL056091, P01 HL065608-090007, P01 HL56091, P01 HL065608, R01 HL074061, R01 HL063706, HL074945, R01 HL63706-04] Funding Source: Medline
  3. NATIONAL CENTER FOR RESEARCH RESOURCES [T32RR007002] Funding Source: NIH RePORTER
  4. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [P01HL056091, P01HL065608, K08HL074945, R01HL074061, R01HL063706] Funding Source: NIH RePORTER

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Vascular endothelial growth factor (VEGF) not only regulates angiogenesis, vascular permeability, and vasodilation but also promotes vascular inflammation. However, the molecular basis for the proinflammatory effects of VEGF is not understood. We now show that VEGF activates endothelial cell exocytosis of Weibel-Palade bodies, releasing vasoactive substances capable of causing vascular thrombosis and inflammation. VEGF triggers endothelial exocytosis in part through calcium and phospholipase C-gamma (PLC-gamma) signal transduction. However, VEGF also modulates endothelial cell exocytosis by activating endothelial nitric oxide synthase (eNOS) production of nitric oxide (NO), which nitrosylates N-ethylmaleimide sensitive factor (NSF) and inhibits exocytosis. Thus, VEGF plays a dual role in regulating endothelial exocytosis, triggering pathways that both promote and inhibit endothelial exocytosis. Regulation of endothelial exocytosis may explain part of the proinflammatory effects of VEGF. (C) 2005 by The American Society of Hematology.

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