VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death
Amyotrophic lateral sclerosis (ALS) is an incurable degenerative disorder of motoneurons. We recently reported that reduced expression of Vegfa causes ALS-like motoneuron degeneration in Vegfa δ/δ mice. In a meta-analysis of over 900 individuals from Sweden and over 1,000 individuals from Belgium an...
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| Vydané v: | Nature genetics Ročník 34; číslo 4; s. 383 - 394 |
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| Hlavní autori: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | English |
| Vydavateľské údaje: |
New York
Nature Publishing Group US
01.08.2003
Nature Publishing Group |
| Predmet: | |
| ISSN: | 1061-4036, 1546-1718 |
| On-line prístup: | Získať plný text |
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| Shrnutí: | Amyotrophic lateral sclerosis (ALS) is an incurable degenerative disorder of motoneurons. We recently reported that reduced expression of
Vegfa
causes ALS-like motoneuron degeneration in
Vegfa
δ/δ
mice. In a meta-analysis of over 900 individuals from Sweden and over 1,000 individuals from Belgium and England, we now report that subjects homozygous with respect to the haplotypes −2,578A/−1,154A/−634G or −2,578A/−1,154G/−634G in the
VEGF
promoter/leader sequence had a 1.8 times greater risk of ALS (
P
= 0.00004). These 'at-risk' haplotypes lowered circulating VEGF levels
in vivo
and reduced
VEGF
gene transcription, IRES-mediated
VEGF
expression and translation of a novel large-VEGF isoform (L-VEGF)
in vivo
. Moreover,
SOD1
G93A
mice crossbred with
Vegfa
δ/δ
mice died earlier due to more severe motoneuron degeneration. Vegfa
δ/δ
mice were unusually susceptible to persistent paralysis after spinal cord ischemia, and treatment with Vegfa protected mice against ischemic motoneuron death. These findings indicate that
VEGF
is a modifier of motoneuron degeneration in human ALS and unveil a therapeutic potential of Vegfa for stressed motoneurons in mice. |
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| Bibliografia: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-1 content type line 23 |
| ISSN: | 1061-4036 1546-1718 |
| DOI: | 10.1038/ng1211 |