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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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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 |
format | Online Article Text |
id | pubmed-5517148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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