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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
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.
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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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