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A mathematical model explains saturating axon guidance responses to molecular gradients

Correct wiring is crucial for the proper functioning of the nervous system. Molecular gradients provide critical signals to guide growth cones, which are the motile tips of developing axons, to their targets. However, in vitro, growth cones trace highly stochastic trajectories, and exactly how molec...

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Autores principales: Nguyen, Huyen, Dayan, Peter, Pujic, Zac, Cooper-White, Justin, Goodhill, Geoffrey J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4755759/
https://www.ncbi.nlm.nih.gov/pubmed/26830461
http://dx.doi.org/10.7554/eLife.12248
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author Nguyen, Huyen
Dayan, Peter
Pujic, Zac
Cooper-White, Justin
Goodhill, Geoffrey J
author_facet Nguyen, Huyen
Dayan, Peter
Pujic, Zac
Cooper-White, Justin
Goodhill, Geoffrey J
author_sort Nguyen, Huyen
collection PubMed
description Correct wiring is crucial for the proper functioning of the nervous system. Molecular gradients provide critical signals to guide growth cones, which are the motile tips of developing axons, to their targets. However, in vitro, growth cones trace highly stochastic trajectories, and exactly how molecular gradients bias their movement is unclear. Here, we introduce a mathematical model based on persistence, bias, and noise to describe this behaviour, constrained directly by measurements of the detailed statistics of growth cone movements in both attractive and repulsive gradients in a microfluidic device. This model provides a mathematical explanation for why average axon turning angles in gradients in vitro saturate very rapidly with time at relatively small values. This work introduces the most accurate predictive model of growth cone trajectories to date, and deepens our understanding of axon guidance events both in vitro and in vivo. DOI: http://dx.doi.org/10.7554/eLife.12248.001
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spelling pubmed-47557592016-02-18 A mathematical model explains saturating axon guidance responses to molecular gradients Nguyen, Huyen Dayan, Peter Pujic, Zac Cooper-White, Justin Goodhill, Geoffrey J eLife Neuroscience Correct wiring is crucial for the proper functioning of the nervous system. Molecular gradients provide critical signals to guide growth cones, which are the motile tips of developing axons, to their targets. However, in vitro, growth cones trace highly stochastic trajectories, and exactly how molecular gradients bias their movement is unclear. Here, we introduce a mathematical model based on persistence, bias, and noise to describe this behaviour, constrained directly by measurements of the detailed statistics of growth cone movements in both attractive and repulsive gradients in a microfluidic device. This model provides a mathematical explanation for why average axon turning angles in gradients in vitro saturate very rapidly with time at relatively small values. This work introduces the most accurate predictive model of growth cone trajectories to date, and deepens our understanding of axon guidance events both in vitro and in vivo. DOI: http://dx.doi.org/10.7554/eLife.12248.001 eLife Sciences Publications, Ltd 2016-02-02 /pmc/articles/PMC4755759/ /pubmed/26830461 http://dx.doi.org/10.7554/eLife.12248 Text en © 2016, Nguyen 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 Neuroscience
Nguyen, Huyen
Dayan, Peter
Pujic, Zac
Cooper-White, Justin
Goodhill, Geoffrey J
A mathematical model explains saturating axon guidance responses to molecular gradients
title A mathematical model explains saturating axon guidance responses to molecular gradients
title_full A mathematical model explains saturating axon guidance responses to molecular gradients
title_fullStr A mathematical model explains saturating axon guidance responses to molecular gradients
title_full_unstemmed A mathematical model explains saturating axon guidance responses to molecular gradients
title_short A mathematical model explains saturating axon guidance responses to molecular gradients
title_sort mathematical model explains saturating axon guidance responses to molecular gradients
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4755759/
https://www.ncbi.nlm.nih.gov/pubmed/26830461
http://dx.doi.org/10.7554/eLife.12248
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