EphA3 expressed in the chicken tectum stimulates Nasal retinal ganglion cell axon growth and is required for retinotectal topographic map formation

Background: Retinotopic projection onto the tectum/colliculus constitutes the most studied model of topographic mapping and Eph receptors and their ligands, the ephrins, are the best characterized molecular system involved in this process. Ephrin-As, expressed in an increasing rostro-caudal gradient...

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Autores principales: Ortalli, A.L., Fiore, L., Di Napoli, J., Rapacioli, M., Salierno, M., Etchenique, R., Flores, V., Sanchez, V., Carri, N.G., Scicolone, G.
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_19326203_v7_n6_p_Ortalli
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spelling todo:paper_19326203_v7_n6_p_Ortalli2023-10-03T16:35:22Z EphA3 expressed in the chicken tectum stimulates Nasal retinal ganglion cell axon growth and is required for retinotectal topographic map formation Ortalli, A.L. Fiore, L. Di Napoli, J. Rapacioli, M. Salierno, M. Etchenique, R. Flores, V. Sanchez, V. Carri, N.G. Scicolone, G. ephrin receptor A3 animal cell animal cell culture animal tissue article cell stimulation chicken concentration response controlled study embryo filopodium human human cell in vitro study in vivo study nasal retina ganglion cell nerve fiber growth nonhuman nose optic nerve fiber optic tectum protein expression protein function protein localization retina ganglion cell retinotectal projection tissue distribution Animals Axons Blotting, Western Cells, Cultured Chick Embryo Chickens Green Fluorescent Proteins HEK293 Cells Humans Immunohistochemistry Microscopy, Confocal Phosphorylation Receptor, EphA3 Retina Retinal Ganglion Cells Superior Colliculi Tectum Mesencephali Time Factors Time-Lapse Imaging Tissue Culture Techniques Tyrosine Visual Pathways Background: Retinotopic projection onto the tectum/colliculus constitutes the most studied model of topographic mapping and Eph receptors and their ligands, the ephrins, are the best characterized molecular system involved in this process. Ephrin-As, expressed in an increasing rostro-caudal gradient in the tectum/colliculus, repel temporal retinal ganglion cell (RGC) axons from the caudal tectum and inhibit their branching posterior to their termination zones. However, there are conflicting data regarding the nature of the second force that guides nasal axons to invade and branch only in the caudal tectum/colliculus. The predominant model postulates that this second force is produced by a decreasing rostro-caudal gradient of EphA7 which repels nasal optic fibers and prevents their branching in the rostral tectum/colliculus. However, as optic fibers invade the tectum/colliculus growing throughout this gradient, this model cannot explain how the axons grow throughout this repellent molecule. Methodology/Principal Findings: By using chicken retinal cultures we showed that EphA3 ectodomain stimulates nasal RGC axon growth in a concentration dependent way. Moreover, we showed that nasal axons choose growing on EphA3-expressing cells and that EphA3 diminishes the density of interstitial filopodia in nasal RGC axons. Accordingly, in vivo EphA3 ectodomain misexpression directs nasal optic fibers toward the caudal tectum preventing their branching in the rostral tectum. Conclusions: We demonstrated in vitro and in vivo that EphA3 ectodomain (which is expressed in a decreasing rostro-caudal gradient in the tectum) is necessary for topographic mapping by stimulating the nasal axon growth toward the caudal tectum and inhibiting their branching in the rostral tectum. Furthermore, the ability of EphA3 of stimulating axon growth allows understanding how optic fibers invade the tectum growing throughout this molecular gradient. Therefore, opposing tectal gradients of repellent ephrin-As and of axon growth stimulating EphA3 complement each other to map optic fibers along the rostro-caudal tectal axis. © 2012 Ortalli et al. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_19326203_v7_n6_p_Ortalli
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic ephrin receptor A3
animal cell
animal cell culture
animal tissue
article
cell stimulation
chicken
concentration response
controlled study
embryo
filopodium
human
human cell
in vitro study
in vivo study
nasal retina ganglion cell
nerve fiber growth
nonhuman
nose
optic nerve fiber
optic tectum
protein expression
protein function
protein localization
retina ganglion cell
retinotectal projection
tissue distribution
Animals
Axons
Blotting, Western
Cells, Cultured
Chick Embryo
Chickens
Green Fluorescent Proteins
HEK293 Cells
Humans
Immunohistochemistry
Microscopy, Confocal
Phosphorylation
Receptor, EphA3
Retina
Retinal Ganglion Cells
Superior Colliculi
Tectum Mesencephali
Time Factors
Time-Lapse Imaging
Tissue Culture Techniques
Tyrosine
Visual Pathways
spellingShingle ephrin receptor A3
animal cell
animal cell culture
animal tissue
article
cell stimulation
chicken
concentration response
controlled study
embryo
filopodium
human
human cell
in vitro study
in vivo study
nasal retina ganglion cell
nerve fiber growth
nonhuman
nose
optic nerve fiber
optic tectum
protein expression
protein function
protein localization
retina ganglion cell
retinotectal projection
tissue distribution
Animals
Axons
Blotting, Western
Cells, Cultured
Chick Embryo
Chickens
Green Fluorescent Proteins
HEK293 Cells
Humans
Immunohistochemistry
Microscopy, Confocal
Phosphorylation
Receptor, EphA3
Retina
Retinal Ganglion Cells
Superior Colliculi
Tectum Mesencephali
Time Factors
Time-Lapse Imaging
Tissue Culture Techniques
Tyrosine
Visual Pathways
Ortalli, A.L.
Fiore, L.
Di Napoli, J.
Rapacioli, M.
Salierno, M.
Etchenique, R.
Flores, V.
Sanchez, V.
Carri, N.G.
Scicolone, G.
EphA3 expressed in the chicken tectum stimulates Nasal retinal ganglion cell axon growth and is required for retinotectal topographic map formation
topic_facet ephrin receptor A3
animal cell
animal cell culture
animal tissue
article
cell stimulation
chicken
concentration response
controlled study
embryo
filopodium
human
human cell
in vitro study
in vivo study
nasal retina ganglion cell
nerve fiber growth
nonhuman
nose
optic nerve fiber
optic tectum
protein expression
protein function
protein localization
retina ganglion cell
retinotectal projection
tissue distribution
Animals
Axons
Blotting, Western
Cells, Cultured
Chick Embryo
Chickens
Green Fluorescent Proteins
HEK293 Cells
Humans
Immunohistochemistry
Microscopy, Confocal
Phosphorylation
Receptor, EphA3
Retina
Retinal Ganglion Cells
Superior Colliculi
Tectum Mesencephali
Time Factors
Time-Lapse Imaging
Tissue Culture Techniques
Tyrosine
Visual Pathways
description Background: Retinotopic projection onto the tectum/colliculus constitutes the most studied model of topographic mapping and Eph receptors and their ligands, the ephrins, are the best characterized molecular system involved in this process. Ephrin-As, expressed in an increasing rostro-caudal gradient in the tectum/colliculus, repel temporal retinal ganglion cell (RGC) axons from the caudal tectum and inhibit their branching posterior to their termination zones. However, there are conflicting data regarding the nature of the second force that guides nasal axons to invade and branch only in the caudal tectum/colliculus. The predominant model postulates that this second force is produced by a decreasing rostro-caudal gradient of EphA7 which repels nasal optic fibers and prevents their branching in the rostral tectum/colliculus. However, as optic fibers invade the tectum/colliculus growing throughout this gradient, this model cannot explain how the axons grow throughout this repellent molecule. Methodology/Principal Findings: By using chicken retinal cultures we showed that EphA3 ectodomain stimulates nasal RGC axon growth in a concentration dependent way. Moreover, we showed that nasal axons choose growing on EphA3-expressing cells and that EphA3 diminishes the density of interstitial filopodia in nasal RGC axons. Accordingly, in vivo EphA3 ectodomain misexpression directs nasal optic fibers toward the caudal tectum preventing their branching in the rostral tectum. Conclusions: We demonstrated in vitro and in vivo that EphA3 ectodomain (which is expressed in a decreasing rostro-caudal gradient in the tectum) is necessary for topographic mapping by stimulating the nasal axon growth toward the caudal tectum and inhibiting their branching in the rostral tectum. Furthermore, the ability of EphA3 of stimulating axon growth allows understanding how optic fibers invade the tectum growing throughout this molecular gradient. Therefore, opposing tectal gradients of repellent ephrin-As and of axon growth stimulating EphA3 complement each other to map optic fibers along the rostro-caudal tectal axis. © 2012 Ortalli et al.
format JOUR
author Ortalli, A.L.
Fiore, L.
Di Napoli, J.
Rapacioli, M.
Salierno, M.
Etchenique, R.
Flores, V.
Sanchez, V.
Carri, N.G.
Scicolone, G.
author_facet Ortalli, A.L.
Fiore, L.
Di Napoli, J.
Rapacioli, M.
Salierno, M.
Etchenique, R.
Flores, V.
Sanchez, V.
Carri, N.G.
Scicolone, G.
author_sort Ortalli, A.L.
title EphA3 expressed in the chicken tectum stimulates Nasal retinal ganglion cell axon growth and is required for retinotectal topographic map formation
title_short EphA3 expressed in the chicken tectum stimulates Nasal retinal ganglion cell axon growth and is required for retinotectal topographic map formation
title_full EphA3 expressed in the chicken tectum stimulates Nasal retinal ganglion cell axon growth and is required for retinotectal topographic map formation
title_fullStr EphA3 expressed in the chicken tectum stimulates Nasal retinal ganglion cell axon growth and is required for retinotectal topographic map formation
title_full_unstemmed EphA3 expressed in the chicken tectum stimulates Nasal retinal ganglion cell axon growth and is required for retinotectal topographic map formation
title_sort epha3 expressed in the chicken tectum stimulates nasal retinal ganglion cell axon growth and is required for retinotectal topographic map formation
url http://hdl.handle.net/20.500.12110/paper_19326203_v7_n6_p_Ortalli
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