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Centrosome-dependent microtubule modifications set the conditions for axon formation
Microtubule (MT) modifications are critical during axon development, with stable MTs populating the axon. How these modifications are spatially coordinated is unclear. Here, via high-resolution microscopy, we show that early developing neurons have fewer somatic acetylated MTs restricted near the ce...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10150443/ https://www.ncbi.nlm.nih.gov/pubmed/35443171 http://dx.doi.org/10.1016/j.celrep.2022.110686 |
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author | Meka, Durga Praveen Kobler, Oliver Hong, Shuai Friedrich, Carina Meta Wuesthoff, Souhaila Henis, Melad Schwanke, Birgit Krisp, Christoph Schmuelling, Nessa Rueter, René Ruecker, Tabitha Betleja, Ewelina Cheng, Tao Mahjoub, Moe R. Soba, Peter Schlüter, Hartmut Fornasiero, Eugenio F. de Anda, Froylan Calderon |
author_facet | Meka, Durga Praveen Kobler, Oliver Hong, Shuai Friedrich, Carina Meta Wuesthoff, Souhaila Henis, Melad Schwanke, Birgit Krisp, Christoph Schmuelling, Nessa Rueter, René Ruecker, Tabitha Betleja, Ewelina Cheng, Tao Mahjoub, Moe R. Soba, Peter Schlüter, Hartmut Fornasiero, Eugenio F. de Anda, Froylan Calderon |
author_sort | Meka, Durga Praveen |
collection | PubMed |
description | Microtubule (MT) modifications are critical during axon development, with stable MTs populating the axon. How these modifications are spatially coordinated is unclear. Here, via high-resolution microscopy, we show that early developing neurons have fewer somatic acetylated MTs restricted near the centrosome. At later stages, however, acetylated MTs spread out in soma and concentrate in growing axon. Live imaging in early plated neurons of the MT plus-end protein, EB3, show increased displacement and growth rate near the MTOC, suggesting local differences that might support axon selection. Moreover, F-actin disruption in early developing neurons, which show fewer somatic acetylated MTs, does not induce multiple axons, unlike later stages. Overexpression of centrosomal protein 120 (Cep120), which promotes MT acetylation/stabilization, induces multiple axons, while its knockdown downregulates proteins modulating MT dynamics and stability, hampering axon formation. Collectively, we show how centrosome-dependent MT modifications contribute to axon formation. |
format | Online Article Text |
id | pubmed-10150443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-101504432023-05-01 Centrosome-dependent microtubule modifications set the conditions for axon formation Meka, Durga Praveen Kobler, Oliver Hong, Shuai Friedrich, Carina Meta Wuesthoff, Souhaila Henis, Melad Schwanke, Birgit Krisp, Christoph Schmuelling, Nessa Rueter, René Ruecker, Tabitha Betleja, Ewelina Cheng, Tao Mahjoub, Moe R. Soba, Peter Schlüter, Hartmut Fornasiero, Eugenio F. de Anda, Froylan Calderon Cell Rep Article Microtubule (MT) modifications are critical during axon development, with stable MTs populating the axon. How these modifications are spatially coordinated is unclear. Here, via high-resolution microscopy, we show that early developing neurons have fewer somatic acetylated MTs restricted near the centrosome. At later stages, however, acetylated MTs spread out in soma and concentrate in growing axon. Live imaging in early plated neurons of the MT plus-end protein, EB3, show increased displacement and growth rate near the MTOC, suggesting local differences that might support axon selection. Moreover, F-actin disruption in early developing neurons, which show fewer somatic acetylated MTs, does not induce multiple axons, unlike later stages. Overexpression of centrosomal protein 120 (Cep120), which promotes MT acetylation/stabilization, induces multiple axons, while its knockdown downregulates proteins modulating MT dynamics and stability, hampering axon formation. Collectively, we show how centrosome-dependent MT modifications contribute to axon formation. 2022-04-19 /pmc/articles/PMC10150443/ /pubmed/35443171 http://dx.doi.org/10.1016/j.celrep.2022.110686 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Meka, Durga Praveen Kobler, Oliver Hong, Shuai Friedrich, Carina Meta Wuesthoff, Souhaila Henis, Melad Schwanke, Birgit Krisp, Christoph Schmuelling, Nessa Rueter, René Ruecker, Tabitha Betleja, Ewelina Cheng, Tao Mahjoub, Moe R. Soba, Peter Schlüter, Hartmut Fornasiero, Eugenio F. de Anda, Froylan Calderon Centrosome-dependent microtubule modifications set the conditions for axon formation |
title | Centrosome-dependent microtubule modifications set the conditions for axon formation |
title_full | Centrosome-dependent microtubule modifications set the conditions for axon formation |
title_fullStr | Centrosome-dependent microtubule modifications set the conditions for axon formation |
title_full_unstemmed | Centrosome-dependent microtubule modifications set the conditions for axon formation |
title_short | Centrosome-dependent microtubule modifications set the conditions for axon formation |
title_sort | centrosome-dependent microtubule modifications set the conditions for axon formation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10150443/ https://www.ncbi.nlm.nih.gov/pubmed/35443171 http://dx.doi.org/10.1016/j.celrep.2022.110686 |
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