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Extracellular Engrailed participates in the topographic guidance of retinal axons in vivo.
- Source :
-
Neuron [Neuron] 2009 Nov 12; Vol. 64 (3), pp. 355-366. - Publication Year :
- 2009
-
Abstract
- Engrailed transcription factors regulate the expression of guidance cues that pattern retinal axon terminals in the dorsal midbrain. They also act directly to guide axon growth in vitro. We show here that an extracellular En gradient exists in the tectum along the anterior-posterior axis. Neutralizing extracellular Engrailed in vivo with antibodies expressed in the tectum causes temporal axons to map aberrantly to the posterior tectum in chick and Xenopus. Furthermore, posterior membranes from wild-type tecta incubated with anti-Engrailed antibodies or posterior membranes from Engrailed-1 knockout mice exhibit diminished repulsive activity for temporal axons. Since EphrinAs play a major role in anterior-posterior mapping, we tested whether Engrailed cooperates with EphrinA5 in vitro. We find that Engrailed restores full repulsion to axons given subthreshold doses of EphrinA5. Collectively, our results indicate that extracellular Engrailed contributes to retinotectal mapping in vivo by modulating the sensitivity of growth cones to EphrinA.
- Subjects :
- Animals
Chick Embryo
Growth Cones physiology
Homeodomain Proteins genetics
In Vitro Techniques
Mice
Mice, Knockout
Receptors, Eph Family metabolism
Retina embryology
Retina growth & development
Retinal Ganglion Cells physiology
Superior Colliculi embryology
Superior Colliculi growth & development
Visual Pathways embryology
Visual Pathways growth & development
Visual Pathways physiology
Xenopus
Axons physiology
Chemotaxis physiology
Extracellular Space metabolism
Homeodomain Proteins metabolism
Retina physiology
Superior Colliculi physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4199
- Volume :
- 64
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Neuron
- Publication Type :
- Academic Journal
- Accession number :
- 19914184
- Full Text :
- https://doi.org/10.1016/j.neuron.2009.09.018