Literature DB >> 11381259

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

B Oosthuyse1, L Moons, E Storkebaum, H Beck, D Nuyens, K Brusselmans, J Van Dorpe, P Hellings, M Gorselink, S Heymans, G Theilmeier, M Dewerchin, V Laudenbach, P Vermylen, H Raat, T Acker, V Vleminckx, L Van Den Bosch, N Cashman, H Fujisawa, M R Drost, R Sciot, F Bruyninckx, D J Hicklin, C Ince, P Gressens, F Lupu, K H Plate, W Robberecht, J M Herbert, D Collen, P Carmeliet.   

Abstract

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, Vegf165 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.

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Year:  2001        PMID: 11381259     DOI: 10.1038/88842

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  262 in total

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