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Radial somatic F‐actin organization affects growth cone dynamics during early neuronal development

The centrosome is thought to be the major neuronal microtubule‐organizing center (MTOC) in early neuronal development, producing microtubules with a radial organization. In addition, albeit in vitro, recent work showed that isolated centrosomes could serve as an actin‐organizing center, raising the...

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Autores principales: Meka, Durga Praveen, Scharrenberg, Robin, Zhao, Bing, Kobler, Oliver, König, Theresa, Schaefer, Irina, Schwanke, Birgit, Klykov, Sergei, Richter, Melanie, Eggert, Dennis, Windhorst, Sabine, Dotti, Carlos G, Kreutz, Michael R, Mikhaylova, Marina, Calderon de Anda, Froylan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893363/
https://www.ncbi.nlm.nih.gov/pubmed/31650708
http://dx.doi.org/10.15252/embr.201947743
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author Meka, Durga Praveen
Scharrenberg, Robin
Zhao, Bing
Kobler, Oliver
König, Theresa
Schaefer, Irina
Schwanke, Birgit
Klykov, Sergei
Richter, Melanie
Eggert, Dennis
Windhorst, Sabine
Dotti, Carlos G
Kreutz, Michael R
Mikhaylova, Marina
Calderon de Anda, Froylan
author_facet Meka, Durga Praveen
Scharrenberg, Robin
Zhao, Bing
Kobler, Oliver
König, Theresa
Schaefer, Irina
Schwanke, Birgit
Klykov, Sergei
Richter, Melanie
Eggert, Dennis
Windhorst, Sabine
Dotti, Carlos G
Kreutz, Michael R
Mikhaylova, Marina
Calderon de Anda, Froylan
author_sort Meka, Durga Praveen
collection PubMed
description The centrosome is thought to be the major neuronal microtubule‐organizing center (MTOC) in early neuronal development, producing microtubules with a radial organization. In addition, albeit in vitro, recent work showed that isolated centrosomes could serve as an actin‐organizing center, raising the possibility that neuronal development may, in addition, require a centrosome‐based actin radial organization. Here, we report, using super‐resolution microscopy and live‐cell imaging of cultured rodent neurons, F‐actin organization around the centrosome with dynamic F‐actin aster‐like structures with F‐actin fibers extending and retracting actively. Photoactivation/photoconversion experiments and molecular manipulations of F‐actin stability reveal a robust flux of somatic F‐actin toward the cell periphery. Finally, we show that somatic F‐actin intermingles with centrosomal PCM‐1 (pericentriolar material 1 protein) satellites. Knockdown of PCM‐1 and disruption of centrosomal activity not only affect F‐actin dynamics near the centrosome but also in distal growth cones. Collectively, the data show a radial F‐actin organization during early neuronal development, which might be a cellular mechanism for providing peripheral regions with a fast and continuous source of actin polymers, hence sustaining initial neuronal development.
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spelling pubmed-68933632019-12-16 Radial somatic F‐actin organization affects growth cone dynamics during early neuronal development Meka, Durga Praveen Scharrenberg, Robin Zhao, Bing Kobler, Oliver König, Theresa Schaefer, Irina Schwanke, Birgit Klykov, Sergei Richter, Melanie Eggert, Dennis Windhorst, Sabine Dotti, Carlos G Kreutz, Michael R Mikhaylova, Marina Calderon de Anda, Froylan EMBO Rep Articles The centrosome is thought to be the major neuronal microtubule‐organizing center (MTOC) in early neuronal development, producing microtubules with a radial organization. In addition, albeit in vitro, recent work showed that isolated centrosomes could serve as an actin‐organizing center, raising the possibility that neuronal development may, in addition, require a centrosome‐based actin radial organization. Here, we report, using super‐resolution microscopy and live‐cell imaging of cultured rodent neurons, F‐actin organization around the centrosome with dynamic F‐actin aster‐like structures with F‐actin fibers extending and retracting actively. Photoactivation/photoconversion experiments and molecular manipulations of F‐actin stability reveal a robust flux of somatic F‐actin toward the cell periphery. Finally, we show that somatic F‐actin intermingles with centrosomal PCM‐1 (pericentriolar material 1 protein) satellites. Knockdown of PCM‐1 and disruption of centrosomal activity not only affect F‐actin dynamics near the centrosome but also in distal growth cones. Collectively, the data show a radial F‐actin organization during early neuronal development, which might be a cellular mechanism for providing peripheral regions with a fast and continuous source of actin polymers, hence sustaining initial neuronal development. John Wiley and Sons Inc. 2019-10-24 2019-12-05 /pmc/articles/PMC6893363/ /pubmed/31650708 http://dx.doi.org/10.15252/embr.201947743 Text en © 2019 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Meka, Durga Praveen
Scharrenberg, Robin
Zhao, Bing
Kobler, Oliver
König, Theresa
Schaefer, Irina
Schwanke, Birgit
Klykov, Sergei
Richter, Melanie
Eggert, Dennis
Windhorst, Sabine
Dotti, Carlos G
Kreutz, Michael R
Mikhaylova, Marina
Calderon de Anda, Froylan
Radial somatic F‐actin organization affects growth cone dynamics during early neuronal development
title Radial somatic F‐actin organization affects growth cone dynamics during early neuronal development
title_full Radial somatic F‐actin organization affects growth cone dynamics during early neuronal development
title_fullStr Radial somatic F‐actin organization affects growth cone dynamics during early neuronal development
title_full_unstemmed Radial somatic F‐actin organization affects growth cone dynamics during early neuronal development
title_short Radial somatic F‐actin organization affects growth cone dynamics during early neuronal development
title_sort radial somatic f‐actin organization affects growth cone dynamics during early neuronal development
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893363/
https://www.ncbi.nlm.nih.gov/pubmed/31650708
http://dx.doi.org/10.15252/embr.201947743
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