Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degeneration

Hypoxia stimulates angiogenesis through the binding of hypoxia-inducible factors to the hypoxia-response element in the vascular endothelial growth factor ( Vegf ) promotor. Here, we report that deletion of the hypoxia-response element in the Vegf promotor reduced hypoxic Vegf expression in the spin...

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Veröffentlicht in:Nature genetics 2001-06, Vol.28 (2), p.131-138
Hauptverfasser: Oosthuyse, Bert, Moons, Lieve, Storkebaum, Erik, Beck, Heike, Nuyens, Dieter, Brusselmans, Koen, Dorpe, Jo Van, Hellings, Peter, Gorselink, Marchel, Heymans, Stéphane, Theilmeier, Gregor, Dewerchin, Mieke, Laudenbach, Vincent, Vermylen, Patrick, Raat, Harold, Acker, Till, Vleminckx, Vicky, Bosch, Ludo Van Den, Cashman, Neil, Fujisawa, Hajime, Drost, Maarten R., Sciot, Raf, Bruyninckx, Frans, Hicklin, Daniel J, Ince, Can, Gressens, Pierre, Lupu, Florea, Plate, Karl H., Robberecht, Wim, Herbert, Jean-Marc, Collen, Désiré, Carmeliet, Peter
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Sprache:eng
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Zusammenfassung:Hypoxia stimulates angiogenesis through the binding of hypoxia-inducible factors to the hypoxia-response element in the vascular endothelial growth factor ( Vegf ) promotor. Here, we report that deletion of the hypoxia-response element in the Vegf promotor reduced hypoxic Vegf expression in the spinal cord and caused adult-onset progressive motor neuron degeneration, reminiscent of amyotrophic lateral sclerosis. The neurodegeneration seemed to be due to reduced neural vascular perfusion. In addition, Vegf 165 promoted survival of motor neurons during hypoxia through binding to Vegf receptor 2 and neuropilin 1. Acute ischemia is known to cause nonselective neuronal death. Our results indicate that chronic vascular insufficiency and, possibly, insufficient Vegf-dependent neuroprotection lead to the select degeneration of motor neurons.
ISSN:1061-4036
1546-1718
DOI:10.1038/88842