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Structural and Molecular Properties of Insect Type II Motor Axon Terminals

A comparison between the axon terminals of octopaminergic efferent dorsal or ventral unpaired median neurons in either desert locusts (Schistocerca gregaria) or fruit flies (Drosophila melanogaster) across skeletal muscles reveals many similarities. In both species the octopaminergic axon forms bead...

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Autores principales: Stocker, Bettina, Bochow, Christina, Damrau, Christine, Mathejczyk, Thomas, Wolfenberg, Heike, Colomb, Julien, Weber, Claudia, Ramesh, Niraja, Duch, Carsten, Biserova, Natalia M., Sigrist, Stephan, Pflüger, Hans-Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867341/
https://www.ncbi.nlm.nih.gov/pubmed/29615874
http://dx.doi.org/10.3389/fnsys.2018.00005
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author Stocker, Bettina
Bochow, Christina
Damrau, Christine
Mathejczyk, Thomas
Wolfenberg, Heike
Colomb, Julien
Weber, Claudia
Ramesh, Niraja
Duch, Carsten
Biserova, Natalia M.
Sigrist, Stephan
Pflüger, Hans-Joachim
author_facet Stocker, Bettina
Bochow, Christina
Damrau, Christine
Mathejczyk, Thomas
Wolfenberg, Heike
Colomb, Julien
Weber, Claudia
Ramesh, Niraja
Duch, Carsten
Biserova, Natalia M.
Sigrist, Stephan
Pflüger, Hans-Joachim
author_sort Stocker, Bettina
collection PubMed
description A comparison between the axon terminals of octopaminergic efferent dorsal or ventral unpaired median neurons in either desert locusts (Schistocerca gregaria) or fruit flies (Drosophila melanogaster) across skeletal muscles reveals many similarities. In both species the octopaminergic axon forms beaded fibers where the boutons or varicosities form type II terminals in contrast to the neuromuscular junction (NMJ) or type I terminals. These type II terminals are immunopositive for both tyramine and octopamine and, in contrast to the type I terminals, which possess clear synaptic vesicles, only contain dense core vesicles. These dense core vesicles contain octopamine as shown by immunogold methods. With respect to the cytomatrix and active zone peptides the type II terminals exhibit active zone-like accumulations of the scaffold protein Bruchpilot (BRP) only sparsely in contrast to the many accumulations of BRP identifying active zones of NMJ type I terminals. In the fruit fly larva marked dynamic changes of octopaminergic fibers have been reported after short starvation which not only affects the formation of new branches (“synaptopods”) but also affects the type I terminals or NMJs via octopamine-signaling (Koon et al., 2011). Our starvation experiments of Drosophila-larvae revealed a time-dependency of the formation of additional branches. Whereas after 2 h of starvation we find a decrease in “synaptopods”, the increase is significant after 6 h of starvation. In addition, we provide evidence that the release of octopamine from dendritic and/or axonal type II terminals uses a similar synaptic machinery to glutamate release from type I terminals of excitatory motor neurons. Indeed, blocking this canonical synaptic release machinery via RNAi induced downregulation of BRP in neurons with type II terminals leads to flight performance deficits similar to those observed for octopamine mutants or flies lacking this class of neurons (Brembs et al., 2007).
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spelling pubmed-58673412018-04-03 Structural and Molecular Properties of Insect Type II Motor Axon Terminals Stocker, Bettina Bochow, Christina Damrau, Christine Mathejczyk, Thomas Wolfenberg, Heike Colomb, Julien Weber, Claudia Ramesh, Niraja Duch, Carsten Biserova, Natalia M. Sigrist, Stephan Pflüger, Hans-Joachim Front Syst Neurosci Neuroscience A comparison between the axon terminals of octopaminergic efferent dorsal or ventral unpaired median neurons in either desert locusts (Schistocerca gregaria) or fruit flies (Drosophila melanogaster) across skeletal muscles reveals many similarities. In both species the octopaminergic axon forms beaded fibers where the boutons or varicosities form type II terminals in contrast to the neuromuscular junction (NMJ) or type I terminals. These type II terminals are immunopositive for both tyramine and octopamine and, in contrast to the type I terminals, which possess clear synaptic vesicles, only contain dense core vesicles. These dense core vesicles contain octopamine as shown by immunogold methods. With respect to the cytomatrix and active zone peptides the type II terminals exhibit active zone-like accumulations of the scaffold protein Bruchpilot (BRP) only sparsely in contrast to the many accumulations of BRP identifying active zones of NMJ type I terminals. In the fruit fly larva marked dynamic changes of octopaminergic fibers have been reported after short starvation which not only affects the formation of new branches (“synaptopods”) but also affects the type I terminals or NMJs via octopamine-signaling (Koon et al., 2011). Our starvation experiments of Drosophila-larvae revealed a time-dependency of the formation of additional branches. Whereas after 2 h of starvation we find a decrease in “synaptopods”, the increase is significant after 6 h of starvation. In addition, we provide evidence that the release of octopamine from dendritic and/or axonal type II terminals uses a similar synaptic machinery to glutamate release from type I terminals of excitatory motor neurons. Indeed, blocking this canonical synaptic release machinery via RNAi induced downregulation of BRP in neurons with type II terminals leads to flight performance deficits similar to those observed for octopamine mutants or flies lacking this class of neurons (Brembs et al., 2007). Frontiers Media S.A. 2018-03-19 /pmc/articles/PMC5867341/ /pubmed/29615874 http://dx.doi.org/10.3389/fnsys.2018.00005 Text en Copyright © 2018 Stocker, Bochow, Damrau, Mathejczyk, Wolfenberg, Colomb, Weber, Ramesh, Duch, Biserova, Sigrist and Pflüger. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Stocker, Bettina
Bochow, Christina
Damrau, Christine
Mathejczyk, Thomas
Wolfenberg, Heike
Colomb, Julien
Weber, Claudia
Ramesh, Niraja
Duch, Carsten
Biserova, Natalia M.
Sigrist, Stephan
Pflüger, Hans-Joachim
Structural and Molecular Properties of Insect Type II Motor Axon Terminals
title Structural and Molecular Properties of Insect Type II Motor Axon Terminals
title_full Structural and Molecular Properties of Insect Type II Motor Axon Terminals
title_fullStr Structural and Molecular Properties of Insect Type II Motor Axon Terminals
title_full_unstemmed Structural and Molecular Properties of Insect Type II Motor Axon Terminals
title_short Structural and Molecular Properties of Insect Type II Motor Axon Terminals
title_sort structural and molecular properties of insect type ii motor axon terminals
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867341/
https://www.ncbi.nlm.nih.gov/pubmed/29615874
http://dx.doi.org/10.3389/fnsys.2018.00005
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