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Regulation of branching dynamics by axon-intrinsic asymmetries in Tyrosine Kinase Receptor signaling

Axonal branching allows a neuron to connect to several targets, increasing neuronal circuit complexity. While axonal branching is well described, the mechanisms that control it remain largely unknown. We find that in the Drosophila CNS branches develop through a process of excessive growth followed...

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Autores principales: Zschätzsch, Marlen, Oliva, Carlos, Langen, Marion, De Geest, Natalie, Özel, Mehmet Neset, Williamson, W Ryan, Lemon, William C, Soldano, Alessia, Munck, Sebastian, Hiesinger, P Robin, Sanchez-Soriano, Natalia, Hassan, Bassem A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3990184/
https://www.ncbi.nlm.nih.gov/pubmed/24755286
http://dx.doi.org/10.7554/eLife.01699
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author Zschätzsch, Marlen
Oliva, Carlos
Langen, Marion
De Geest, Natalie
Özel, Mehmet Neset
Williamson, W Ryan
Lemon, William C
Soldano, Alessia
Munck, Sebastian
Hiesinger, P Robin
Sanchez-Soriano, Natalia
Hassan, Bassem A
author_facet Zschätzsch, Marlen
Oliva, Carlos
Langen, Marion
De Geest, Natalie
Özel, Mehmet Neset
Williamson, W Ryan
Lemon, William C
Soldano, Alessia
Munck, Sebastian
Hiesinger, P Robin
Sanchez-Soriano, Natalia
Hassan, Bassem A
author_sort Zschätzsch, Marlen
collection PubMed
description Axonal branching allows a neuron to connect to several targets, increasing neuronal circuit complexity. While axonal branching is well described, the mechanisms that control it remain largely unknown. We find that in the Drosophila CNS branches develop through a process of excessive growth followed by pruning. In vivo high-resolution live imaging of developing brains as well as loss and gain of function experiments show that activation of Epidermal Growth Factor Receptor (EGFR) is necessary for branch dynamics and the final branching pattern. Live imaging also reveals that intrinsic asymmetry in EGFR localization regulates the balance between dynamic and static filopodia. Elimination of signaling asymmetry by either loss or gain of EGFR function results in reduced dynamics leading to excessive branch formation. In summary, we propose that the dynamic process of axon branch development is mediated by differential local distribution of signaling receptors. DOI: http://dx.doi.org/10.7554/eLife.01699.001
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spelling pubmed-39901842014-04-24 Regulation of branching dynamics by axon-intrinsic asymmetries in Tyrosine Kinase Receptor signaling Zschätzsch, Marlen Oliva, Carlos Langen, Marion De Geest, Natalie Özel, Mehmet Neset Williamson, W Ryan Lemon, William C Soldano, Alessia Munck, Sebastian Hiesinger, P Robin Sanchez-Soriano, Natalia Hassan, Bassem A eLife Neuroscience Axonal branching allows a neuron to connect to several targets, increasing neuronal circuit complexity. While axonal branching is well described, the mechanisms that control it remain largely unknown. We find that in the Drosophila CNS branches develop through a process of excessive growth followed by pruning. In vivo high-resolution live imaging of developing brains as well as loss and gain of function experiments show that activation of Epidermal Growth Factor Receptor (EGFR) is necessary for branch dynamics and the final branching pattern. Live imaging also reveals that intrinsic asymmetry in EGFR localization regulates the balance between dynamic and static filopodia. Elimination of signaling asymmetry by either loss or gain of EGFR function results in reduced dynamics leading to excessive branch formation. In summary, we propose that the dynamic process of axon branch development is mediated by differential local distribution of signaling receptors. DOI: http://dx.doi.org/10.7554/eLife.01699.001 eLife Sciences Publications, Ltd 2014-04-22 /pmc/articles/PMC3990184/ /pubmed/24755286 http://dx.doi.org/10.7554/eLife.01699 Text en Copyright © 2014, Zschätzsch et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Zschätzsch, Marlen
Oliva, Carlos
Langen, Marion
De Geest, Natalie
Özel, Mehmet Neset
Williamson, W Ryan
Lemon, William C
Soldano, Alessia
Munck, Sebastian
Hiesinger, P Robin
Sanchez-Soriano, Natalia
Hassan, Bassem A
Regulation of branching dynamics by axon-intrinsic asymmetries in Tyrosine Kinase Receptor signaling
title Regulation of branching dynamics by axon-intrinsic asymmetries in Tyrosine Kinase Receptor signaling
title_full Regulation of branching dynamics by axon-intrinsic asymmetries in Tyrosine Kinase Receptor signaling
title_fullStr Regulation of branching dynamics by axon-intrinsic asymmetries in Tyrosine Kinase Receptor signaling
title_full_unstemmed Regulation of branching dynamics by axon-intrinsic asymmetries in Tyrosine Kinase Receptor signaling
title_short Regulation of branching dynamics by axon-intrinsic asymmetries in Tyrosine Kinase Receptor signaling
title_sort regulation of branching dynamics by axon-intrinsic asymmetries in tyrosine kinase receptor signaling
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3990184/
https://www.ncbi.nlm.nih.gov/pubmed/24755286
http://dx.doi.org/10.7554/eLife.01699
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