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Ephrin-A/EphA specific co-adaptation as a novel mechanism in topographic axon guidance

Genetic hardwiring during brain development provides computational architectures for innate neuronal processing. Thus, the paradigmatic chick retinotectal projection, due to its neighborhood preserving, topographic organization, establishes millions of parallel channels for incremental visual field...

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Autores principales: Fiederling, Felix, Weschenfelder, Markus, Fritz, Martin, von Philipsborn, Anne, Bastmeyer, Martin, Weth, Franco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5517148/
https://www.ncbi.nlm.nih.gov/pubmed/28722651
http://dx.doi.org/10.7554/eLife.25533
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author Fiederling, Felix
Weschenfelder, Markus
Fritz, Martin
von Philipsborn, Anne
Bastmeyer, Martin
Weth, Franco
author_facet Fiederling, Felix
Weschenfelder, Markus
Fritz, Martin
von Philipsborn, Anne
Bastmeyer, Martin
Weth, Franco
author_sort Fiederling, Felix
collection PubMed
description Genetic hardwiring during brain development provides computational architectures for innate neuronal processing. Thus, the paradigmatic chick retinotectal projection, due to its neighborhood preserving, topographic organization, establishes millions of parallel channels for incremental visual field analysis. Retinal axons receive targeting information from quantitative guidance cue gradients. Surprisingly, novel adaptation assays demonstrate that retinal growth cones robustly adapt towards ephrin-A/EphA forward and reverse signals, which provide the major mapping cues. Computational modeling suggests that topographic accuracy and adaptability, though seemingly incompatible, could be reconciled by a novel mechanism of coupled adaptation of signaling channels. Experimentally, we find such ‘co-adaptation’ in retinal growth cones specifically for ephrin-A/EphA signaling. Co-adaptation involves trafficking of unliganded sensors between the surface membrane and recycling endosomes, and is presumably triggered by changes in the lipid composition of membrane microdomains. We propose that co-adaptative desensitization eventually relies on guidance sensor translocation into cis-signaling endosomes to outbalance repulsive trans-signaling. DOI: http://dx.doi.org/10.7554/eLife.25533.001
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spelling pubmed-55171482017-07-20 Ephrin-A/EphA specific co-adaptation as a novel mechanism in topographic axon guidance Fiederling, Felix Weschenfelder, Markus Fritz, Martin von Philipsborn, Anne Bastmeyer, Martin Weth, Franco eLife Developmental Biology and Stem Cells Genetic hardwiring during brain development provides computational architectures for innate neuronal processing. Thus, the paradigmatic chick retinotectal projection, due to its neighborhood preserving, topographic organization, establishes millions of parallel channels for incremental visual field analysis. Retinal axons receive targeting information from quantitative guidance cue gradients. Surprisingly, novel adaptation assays demonstrate that retinal growth cones robustly adapt towards ephrin-A/EphA forward and reverse signals, which provide the major mapping cues. Computational modeling suggests that topographic accuracy and adaptability, though seemingly incompatible, could be reconciled by a novel mechanism of coupled adaptation of signaling channels. Experimentally, we find such ‘co-adaptation’ in retinal growth cones specifically for ephrin-A/EphA signaling. Co-adaptation involves trafficking of unliganded sensors between the surface membrane and recycling endosomes, and is presumably triggered by changes in the lipid composition of membrane microdomains. We propose that co-adaptative desensitization eventually relies on guidance sensor translocation into cis-signaling endosomes to outbalance repulsive trans-signaling. DOI: http://dx.doi.org/10.7554/eLife.25533.001 eLife Sciences Publications, Ltd 2017-07-19 /pmc/articles/PMC5517148/ /pubmed/28722651 http://dx.doi.org/10.7554/eLife.25533 Text en © 2017, Fiederling et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology and Stem Cells
Fiederling, Felix
Weschenfelder, Markus
Fritz, Martin
von Philipsborn, Anne
Bastmeyer, Martin
Weth, Franco
Ephrin-A/EphA specific co-adaptation as a novel mechanism in topographic axon guidance
title Ephrin-A/EphA specific co-adaptation as a novel mechanism in topographic axon guidance
title_full Ephrin-A/EphA specific co-adaptation as a novel mechanism in topographic axon guidance
title_fullStr Ephrin-A/EphA specific co-adaptation as a novel mechanism in topographic axon guidance
title_full_unstemmed Ephrin-A/EphA specific co-adaptation as a novel mechanism in topographic axon guidance
title_short Ephrin-A/EphA specific co-adaptation as a novel mechanism in topographic axon guidance
title_sort ephrin-a/epha specific co-adaptation as a novel mechanism in topographic axon guidance
topic Developmental Biology and Stem Cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5517148/
https://www.ncbi.nlm.nih.gov/pubmed/28722651
http://dx.doi.org/10.7554/eLife.25533
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