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Direct stimulation of adult neural stem cells in vitro and neurogenesis in vivo by vascular endothelial growth factor.

Artikel i vetenskaplig tidskrift
Författare Anne Schänzer
Frank-Peter Wachs
Daniel Wilhelm
Till Acker
Christiana M Cooper-Kuhn
Heike Beck
Jürgen Winkler
Ludwig Aigner
Karl H Plate
Hans-Georg Kuhn
Publicerad i Brain pathology (Zurich, Switzerland)
Volym 14
Nummer/häfte 3
Sidor 237-48
ISSN 1015-6305
Publiceringsår 2004
Publicerad vid Institutionen för klinisk neurovetenskap
Sidor 237-48
Språk en
Länkar www.ncbi.nlm.nih.gov/entrez/query.f...
Ämnesord Animals, Apoptosis, drug effects, Blood-Brain Barrier, drug effects, Brain, drug effects, Cell Survival, drug effects, Female, Immunohistochemistry, In Situ Nick-End Labeling, Injections, Intraventricular, Neurons, drug effects, Rats, Rats, Inbred F344, Reverse Transcriptase Polymerase Chain Reaction, Stem Cells, drug effects, Vascular Endothelial Growth Factor A, pharmacology, Vascular Endothelial Growth Factor Receptor-2, biosynthesis, drug effects
Ämneskategorier Medicin och Hälsovetenskap

Sammanfattning

Hypoxia as well as global and focal ischemia are strong activators of neurogenesis in the adult mammalian central nervous system. Here we show that the hypoxia-inducible vascular endothelial growth factor (VEGF) and its receptor VEGFR-2/Flk-1 are expressed in clonally-derived adult rat neural stem cells in vitro. VEGF stimulated the expansion of neural stem cells whereas blockade of VEGFR-2/Flk-1-kinase activity reduced neural stem cell expansion. VEGF was also infused into the lateral ventricle to study changes in neurogenesis in the ventricle wall, olfactory bulb and hippocampus. Using a low dose (2.4 ng/d) to avoid endothelial proliferation and changes in vascular permeability, VEGF stimulated adult neurogenesis in vivo. After VEGF infusion, we observed reduced apoptosis but unaltered proliferation suggesting a survival promoting effect of VEGF in neural progenitor cells. Strong expression of VEGFR-2/Flk-1 was detected in the ventricle wall adjacent to the choroid plexus, a site of significant VEGF production, which suggests a paracrine function of endogenous VEGF on neural stem cells in vivo. We propose that VEGF acts as a trophic factor for neural stem cells in vitro and for sustained neurogenesis in the adult nervous system.These findings may have implications for the pathogenesis and therapy of neurodegenerative diseases.

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