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VEGF mediates commissural axon chemoattraction through its receptor Flk1.
- Source :
-
Neuron [Neuron] 2011 Jun 09; Vol. 70 (5), pp. 966-78. - Publication Year :
- 2011
-
Abstract
- Growing axons are guided to their targets by attractive and repulsive cues. In the developing spinal cord, Netrin-1 and Shh guide commissural axons toward the midline. However, the combined inhibition of their activity in commissural axon turning assays does not completely abrogate turning toward floor plate tissue, suggesting that additional guidance cues are present. Here we show that the prototypic angiogenic factor VEGF is secreted by the floor plate and is a chemoattractant for commissural axons in vitro and in vivo. Inactivation of Vegf in the floor plate or of its receptor Flk1 in commissural neurons causes axon guidance defects, whereas Flk1 blockade inhibits turning of axons to VEGF in vitro. Similar to Shh and Netrin-1, VEGF-mediated commissural axon guidance requires the activity of Src family kinases. Our results identify VEGF and Flk1 as a novel ligand/receptor pair controlling commissural axon guidance.<br /> (Copyright © 2011 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Cells, Cultured
Chemotaxis genetics
Embryo, Mammalian
Enzyme-Linked Immunosorbent Assay methods
Glycoside Hydrolases metabolism
Growth Cones metabolism
Hedgehog Proteins metabolism
In Vitro Techniques
Mice
Mice, Transgenic
Nerve Growth Factors metabolism
Netrin-1
Neurons cytology
Rats
Rats, Sprague-Dawley
Rats, Wistar
Tumor Suppressor Proteins metabolism
Vascular Endothelial Growth Factor A genetics
Vascular Endothelial Growth Factor Receptor-2 genetics
Wnt1 Protein genetics
Axons physiology
Chemotaxis physiology
Optic Chiasm cytology
Vascular Endothelial Growth Factor A metabolism
Vascular Endothelial Growth Factor Receptor-2 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4199
- Volume :
- 70
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Neuron
- Publication Type :
- Academic Journal
- Accession number :
- 21658588
- Full Text :
- https://doi.org/10.1016/j.neuron.2011.04.014