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Achieving functional neuronal dendrite structure through sequential stochastic growth and retraction
Class I ventral posterior dendritic arborisation (c1vpda) proprioceptive sensory neurons respond to contractions in the Drosophila larval body wall during crawling. Their dendritic branches run along the direction of contraction, possibly a functional requirement to maximise membrane curvature durin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837678/ https://www.ncbi.nlm.nih.gov/pubmed/33241995 http://dx.doi.org/10.7554/eLife.60920 |
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author | Ferreira Castro, André Baltruschat, Lothar Stürner, Tomke Bahrami, Amirhoushang Jedlicka, Peter Tavosanis, Gaia Cuntz, Hermann |
author_facet | Ferreira Castro, André Baltruschat, Lothar Stürner, Tomke Bahrami, Amirhoushang Jedlicka, Peter Tavosanis, Gaia Cuntz, Hermann |
author_sort | Ferreira Castro, André |
collection | PubMed |
description | Class I ventral posterior dendritic arborisation (c1vpda) proprioceptive sensory neurons respond to contractions in the Drosophila larval body wall during crawling. Their dendritic branches run along the direction of contraction, possibly a functional requirement to maximise membrane curvature during crawling contractions. Although the molecular machinery of dendritic patterning in c1vpda has been extensively studied, the process leading to the precise elaboration of their comb-like shapes remains elusive. Here, to link dendrite shape with its proprioceptive role, we performed long-term, non-invasive, in vivo time-lapse imaging of c1vpda embryonic and larval morphogenesis to reveal a sequence of differentiation stages. We combined computer models and dendritic branch dynamics tracking to propose that distinct sequential phases of stochastic growth and retraction achieve efficient dendritic trees both in terms of wire and function. Our study shows how dendrite growth balances structure–function requirements, shedding new light on general principles of self-organisation in functionally specialised dendrites. |
format | Online Article Text |
id | pubmed-7837678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-78376782021-01-27 Achieving functional neuronal dendrite structure through sequential stochastic growth and retraction Ferreira Castro, André Baltruschat, Lothar Stürner, Tomke Bahrami, Amirhoushang Jedlicka, Peter Tavosanis, Gaia Cuntz, Hermann eLife Developmental Biology Class I ventral posterior dendritic arborisation (c1vpda) proprioceptive sensory neurons respond to contractions in the Drosophila larval body wall during crawling. Their dendritic branches run along the direction of contraction, possibly a functional requirement to maximise membrane curvature during crawling contractions. Although the molecular machinery of dendritic patterning in c1vpda has been extensively studied, the process leading to the precise elaboration of their comb-like shapes remains elusive. Here, to link dendrite shape with its proprioceptive role, we performed long-term, non-invasive, in vivo time-lapse imaging of c1vpda embryonic and larval morphogenesis to reveal a sequence of differentiation stages. We combined computer models and dendritic branch dynamics tracking to propose that distinct sequential phases of stochastic growth and retraction achieve efficient dendritic trees both in terms of wire and function. Our study shows how dendrite growth balances structure–function requirements, shedding new light on general principles of self-organisation in functionally specialised dendrites. eLife Sciences Publications, Ltd 2020-11-26 /pmc/articles/PMC7837678/ /pubmed/33241995 http://dx.doi.org/10.7554/eLife.60920 Text en © 2020, Ferreira Castro et al http://creativecommons.org/licenses/by/4.0/ 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 Ferreira Castro, André Baltruschat, Lothar Stürner, Tomke Bahrami, Amirhoushang Jedlicka, Peter Tavosanis, Gaia Cuntz, Hermann Achieving functional neuronal dendrite structure through sequential stochastic growth and retraction |
title | Achieving functional neuronal dendrite structure through sequential stochastic growth and retraction |
title_full | Achieving functional neuronal dendrite structure through sequential stochastic growth and retraction |
title_fullStr | Achieving functional neuronal dendrite structure through sequential stochastic growth and retraction |
title_full_unstemmed | Achieving functional neuronal dendrite structure through sequential stochastic growth and retraction |
title_short | Achieving functional neuronal dendrite structure through sequential stochastic growth and retraction |
title_sort | achieving functional neuronal dendrite structure through sequential stochastic growth and retraction |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837678/ https://www.ncbi.nlm.nih.gov/pubmed/33241995 http://dx.doi.org/10.7554/eLife.60920 |
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