Effects of vascular endothelial growth factor (VEGF) on motor neuron degeneration

Both in mice and humans, low expression levels of vascular endothelial growth factor (VEGF) are linked to adult-onset motor neuron disease or amyotrophic lateral sclerosis (ALS). The mechanism through which reduced VEGF levels result in this phenotype is unknown. We therefore examined the direct eff...

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Published inNeurobiology of disease Vol. 17; no. 1; pp. 21 - 28
Main Authors Van Den Bosch, Ludo, Storkebaum, Erik, Vleminckx, Vicky, Moons, Lieve, Vanopdenbosch, Ludo, Scheveneels, Wendy, Carmeliet, Peter, Robberecht, Wim
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.10.2004
Elsevier
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Abstract Both in mice and humans, low expression levels of vascular endothelial growth factor (VEGF) are linked to adult-onset motor neuron disease or amyotrophic lateral sclerosis (ALS). The mechanism through which reduced VEGF levels result in this phenotype is unknown. We therefore examined the direct effects of VEGF on motor neurons and found VEGF to have a direct neurotrophic effect on motor neurons in vitro. Survival and vulnerability to excitotoxicity of motor neurons from VEGF δ/δ mice was however similar to that of motor neurons from non-transgenic littermates. The VEGF concentration in the spinal cord of mutant (G93A) SOD1 mice was not different from that found in wild-type SOD1 overexpressing mice. Upregulation of VEGF in the spinal cord, by housing mutant (G93A) SOD1 mice in hypoxic conditions, did not affect their life span. Our results show that VEGF is a neurotrophic factor for motor neurons in vitro, and shortage of this neurotrophic factor may contribute to the motor neuron death observed in humans and animals with low VEGF expression levels.
AbstractList Both in mice and humans, low expression levels of vascular endothelial growth factor (VEGF) are linked to adult-onset motor neuron disease or amyotrophic lateral sclerosis (ALS). The mechanism through which reduced VEGF levels result in this phenotype is unknown. We therefore examined the direct effects of VEGF on motor neurons and found VEGF to have a direct neurotrophic effect on motor neurons in vitro. Survival and vulnerability to excitotoxicity of motor neurons from VEGF(delta/delta) mice was however similar to that of motor neurons from non-transgenic littermates. The VEGF concentration in the spinal cord of mutant (G93A) SOD1 mice was not different from that found in wild-type SOD1 overexpressing mice. Upregulation of VEGF in the spinal cord, by housing mutant (G93A) SOD1 mice in hypoxic conditions, did not affect their life span. Our results show that VEGF is a neurotrophic factor for motor neurons in vitro, and shortage of this neurotrophic factor may contribute to the motor neuron death observed in humans and animals with low VEGF expression levels.
Both in mice and humans, low expression levels of vascular endothelial growth factor (VEGF) are linked to adult-onset motor neuron disease or amyotrophic lateral sclerosis (ALS). The mechanism through which reduced VEGF levels result in this phenotype is unknown. We therefore examined the direct effects of VEGF on motor neurons and found VEGF to have a direct neurotrophic effect on motor neurons in vitro. Survival and vulnerability to excitotoxicity of motor neurons from VEGFδ/δ mice was however similar to that of motor neurons from non-transgenic littermates. The VEGF concentration in the spinal cord of mutant (G93A) SOD1 mice was not different from that found in wild-type SOD1 overexpressing mice. Upregulation of VEGF in the spinal cord, by housing mutant (G93A) SOD1 mice in hypoxic conditions, did not affect their life span. Our results show that VEGF is a neurotrophic factor for motor neurons in vitro, and shortage of this neurotrophic factor may contribute to the motor neuron death observed in humans and animals with low VEGF expression levels.
Both in mice and humans, low expression levels of vascular endothelial growth factor (VEGF) are linked to adult-onset motor neuron disease or amyotrophic lateral sclerosis (ALS). The mechanism through which reduced VEGF levels result in this phenotype is unknown. We therefore examined the direct effects of VEGF on motor neurons and found VEGF to have a direct neurotrophic effect on motor neurons in vitro. Survival and vulnerability to excitotoxicity of motor neurons from VEGF δ/δ mice was however similar to that of motor neurons from non-transgenic littermates. The VEGF concentration in the spinal cord of mutant (G93A) SOD1 mice was not different from that found in wild-type SOD1 overexpressing mice. Upregulation of VEGF in the spinal cord, by housing mutant (G93A) SOD1 mice in hypoxic conditions, did not affect their life span. Our results show that VEGF is a neurotrophic factor for motor neurons in vitro, and shortage of this neurotrophic factor may contribute to the motor neuron death observed in humans and animals with low VEGF expression levels.
Author Storkebaum, Erik
Robberecht, Wim
Van Den Bosch, Ludo
Vleminckx, Vicky
Vanopdenbosch, Ludo
Scheveneels, Wendy
Carmeliet, Peter
Moons, Lieve
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  givenname: Erik
  surname: Storkebaum
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  organization: Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology, School of Medicine, University of Leuven, Leuven, Belgium
– sequence: 3
  givenname: Vicky
  surname: Vleminckx
  fullname: Vleminckx, Vicky
  organization: Laboratory for Neurobiology, Department of Experimental Neurology, School of Medicine, University of Leuven, Leuven, Belgium
– sequence: 4
  givenname: Lieve
  surname: Moons
  fullname: Moons, Lieve
  organization: Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology, School of Medicine, University of Leuven, Leuven, Belgium
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  givenname: Wendy
  surname: Scheveneels
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– sequence: 7
  givenname: Peter
  surname: Carmeliet
  fullname: Carmeliet, Peter
  organization: Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology, School of Medicine, University of Leuven, Leuven, Belgium
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  givenname: Wim
  surname: Robberecht
  fullname: Robberecht, Wim
  email: Wim.Robberecht@uz.kuleuven.ac.be
  organization: Laboratory for Neurobiology, Department of Experimental Neurology, School of Medicine, University of Leuven, Leuven, Belgium
BackLink https://www.ncbi.nlm.nih.gov/pubmed/15350962$$D View this record in MEDLINE/PubMed
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Keywords ALS
Neurotrophic factor
Amyotrophic lateral sclerosis
Hypoxia
Motor neuron
Vascular endothelial growth factor
Language English
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Snippet Both in mice and humans, low expression levels of vascular endothelial growth factor (VEGF) are linked to adult-onset motor neuron disease or amyotrophic...
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SubjectTerms ALS
Amyotrophic lateral sclerosis
Animals
Cell Survival - drug effects
Cell Survival - physiology
Cells, Cultured
Dose-Response Relationship, Drug
Hypoxia
Mice
Mice, Inbred C57BL
Mice, Transgenic
Motor neuron
Motor Neurons - drug effects
Motor Neurons - metabolism
Nerve Degeneration - drug therapy
Nerve Degeneration - genetics
Nerve Degeneration - metabolism
Neurotrophic factor
Rats
Rats, Wistar
Superoxide Dismutase - biosynthesis
Superoxide Dismutase - genetics
Superoxide Dismutase-1
Vascular endothelial growth factor
Vascular Endothelial Growth Factor A - biosynthesis
Vascular Endothelial Growth Factor A - genetics
Vascular Endothelial Growth Factor A - pharmacology
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Title Effects of vascular endothelial growth factor (VEGF) on motor neuron degeneration
URI https://dx.doi.org/10.1016/j.nbd.2004.06.004
https://www.ncbi.nlm.nih.gov/pubmed/15350962
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