Cargando…
Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis
Dendritic morphogenesis requires dynamic microtubules (MTs) to form a coordinated cytoskeletal network during development. Dynamic MTs are characterized by their number, polarity and speed of polymerization. Previous studies described a correlation between anterograde MT growth and terminal branch e...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496546/ https://www.ncbi.nlm.nih.gov/pubmed/34609266 http://dx.doi.org/10.1080/19336934.2021.1976033 |
_version_ | 1784579774710022144 |
---|---|
author | Hu, Chun Feng, Pan Chen, Meilan Tang, Yan Soba, Peter |
author_facet | Hu, Chun Feng, Pan Chen, Meilan Tang, Yan Soba, Peter |
author_sort | Hu, Chun |
collection | PubMed |
description | Dendritic morphogenesis requires dynamic microtubules (MTs) to form a coordinated cytoskeletal network during development. Dynamic MTs are characterized by their number, polarity and speed of polymerization. Previous studies described a correlation between anterograde MT growth and terminal branch extension in Drosophila dendritic arborization (da) neurons, suggesting a model that anterograde MT polymerization provides a driving force for dendritic branching. We recently found that the Ste20-like kinase Tao specifically regulates dendritic branching by controlling the number of dynamic MTs in a kinase activity-dependent fashion, without affecting MT polarity or speed. This finding raises the interesting question of how MT dynamics affects dendritic morphogenesis, and if Tao kinase activity is developmentally regulated to coordinate MT dynamics and dendritic morphogenesis. We explored the possible correlation between MT dynamics and dendritic morphogenesis together with the activity changes of Tao kinase in C1da and C4da neurons during larval development. Our data show that spatiotemporal changes in the number of dynamic MTs, but not polarity or polymerization speed, correlate with dendritic branching and Tao kinase activity. Our findings suggest that Tao kinase limits dendritic branching by controlling the abundance of dynamic MTs and we propose a novel model on how regulation of MT dynamics might influence dendritic morphogenesis. |
format | Online Article Text |
id | pubmed-8496546 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-84965462021-10-08 Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis Hu, Chun Feng, Pan Chen, Meilan Tang, Yan Soba, Peter Fly (Austin) Extra View Dendritic morphogenesis requires dynamic microtubules (MTs) to form a coordinated cytoskeletal network during development. Dynamic MTs are characterized by their number, polarity and speed of polymerization. Previous studies described a correlation between anterograde MT growth and terminal branch extension in Drosophila dendritic arborization (da) neurons, suggesting a model that anterograde MT polymerization provides a driving force for dendritic branching. We recently found that the Ste20-like kinase Tao specifically regulates dendritic branching by controlling the number of dynamic MTs in a kinase activity-dependent fashion, without affecting MT polarity or speed. This finding raises the interesting question of how MT dynamics affects dendritic morphogenesis, and if Tao kinase activity is developmentally regulated to coordinate MT dynamics and dendritic morphogenesis. We explored the possible correlation between MT dynamics and dendritic morphogenesis together with the activity changes of Tao kinase in C1da and C4da neurons during larval development. Our data show that spatiotemporal changes in the number of dynamic MTs, but not polarity or polymerization speed, correlate with dendritic branching and Tao kinase activity. Our findings suggest that Tao kinase limits dendritic branching by controlling the abundance of dynamic MTs and we propose a novel model on how regulation of MT dynamics might influence dendritic morphogenesis. Taylor & Francis 2021-10-05 /pmc/articles/PMC8496546/ /pubmed/34609266 http://dx.doi.org/10.1080/19336934.2021.1976033 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Extra View Hu, Chun Feng, Pan Chen, Meilan Tang, Yan Soba, Peter Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis |
title | Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis |
title_full | Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis |
title_fullStr | Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis |
title_full_unstemmed | Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis |
title_short | Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis |
title_sort | spatiotemporal changes in microtubule dynamics during dendritic morphogenesis |
topic | Extra View |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496546/ https://www.ncbi.nlm.nih.gov/pubmed/34609266 http://dx.doi.org/10.1080/19336934.2021.1976033 |
work_keys_str_mv | AT huchun spatiotemporalchangesinmicrotubuledynamicsduringdendriticmorphogenesis AT fengpan spatiotemporalchangesinmicrotubuledynamicsduringdendriticmorphogenesis AT chenmeilan spatiotemporalchangesinmicrotubuledynamicsduringdendriticmorphogenesis AT tangyan spatiotemporalchangesinmicrotubuledynamicsduringdendriticmorphogenesis AT sobapeter spatiotemporalchangesinmicrotubuledynamicsduringdendriticmorphogenesis |