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Terminal Schwann cell and vacant site mediated synapse elimination at developing neuromuscular junctions

Synapses undergo transition from polyinnervation by multiple axons to single innervation a few weeks after birth. Synaptic activity of axons and interaxonal competition are thought to drive this developmental synapse elimination and tested as key parameters in quantitative models for further underst...

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Autores principales: Jung, Jae Hoon, Smith, Ian, Mikesh, Michelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901572/
https://www.ncbi.nlm.nih.gov/pubmed/31819113
http://dx.doi.org/10.1038/s41598-019-55017-w
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author Jung, Jae Hoon
Smith, Ian
Mikesh, Michelle
author_facet Jung, Jae Hoon
Smith, Ian
Mikesh, Michelle
author_sort Jung, Jae Hoon
collection PubMed
description Synapses undergo transition from polyinnervation by multiple axons to single innervation a few weeks after birth. Synaptic activity of axons and interaxonal competition are thought to drive this developmental synapse elimination and tested as key parameters in quantitative models for further understanding. Recent studies of muscle synapses (endplates) show that there are also terminal Schwann cells (tSCs), glial cells associated with motor neurons and their functions, and vacant sites (or vacancies) devoid of tSCs and axons proposing tSCs as key effectors of synapse elimination. However, there is no quantitative model that considers roles of tSCs including vacancies. Here we develop a stochastic model of tSC and vacancy mediated synapse elimination. It employs their areas on individual endplates quantified by electron microscopy-based analyses assuming that vacancies form randomly and are taken over by adjacent axons or tSCs. The model reliably reproduced synapse elimination whereas equal or random probability models, similar to classical interaxonal competition models, did not. Furthermore, the model showed that synapse elimination is accelerated by enhanced synaptic activity of one axon and also by increased areas of vacancies and tSCs suggesting that the areas are important structural correlates of the rate of synapse elimination.
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spelling pubmed-69015722019-12-12 Terminal Schwann cell and vacant site mediated synapse elimination at developing neuromuscular junctions Jung, Jae Hoon Smith, Ian Mikesh, Michelle Sci Rep Article Synapses undergo transition from polyinnervation by multiple axons to single innervation a few weeks after birth. Synaptic activity of axons and interaxonal competition are thought to drive this developmental synapse elimination and tested as key parameters in quantitative models for further understanding. Recent studies of muscle synapses (endplates) show that there are also terminal Schwann cells (tSCs), glial cells associated with motor neurons and their functions, and vacant sites (or vacancies) devoid of tSCs and axons proposing tSCs as key effectors of synapse elimination. However, there is no quantitative model that considers roles of tSCs including vacancies. Here we develop a stochastic model of tSC and vacancy mediated synapse elimination. It employs their areas on individual endplates quantified by electron microscopy-based analyses assuming that vacancies form randomly and are taken over by adjacent axons or tSCs. The model reliably reproduced synapse elimination whereas equal or random probability models, similar to classical interaxonal competition models, did not. Furthermore, the model showed that synapse elimination is accelerated by enhanced synaptic activity of one axon and also by increased areas of vacancies and tSCs suggesting that the areas are important structural correlates of the rate of synapse elimination. Nature Publishing Group UK 2019-12-09 /pmc/articles/PMC6901572/ /pubmed/31819113 http://dx.doi.org/10.1038/s41598-019-55017-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Jung, Jae Hoon
Smith, Ian
Mikesh, Michelle
Terminal Schwann cell and vacant site mediated synapse elimination at developing neuromuscular junctions
title Terminal Schwann cell and vacant site mediated synapse elimination at developing neuromuscular junctions
title_full Terminal Schwann cell and vacant site mediated synapse elimination at developing neuromuscular junctions
title_fullStr Terminal Schwann cell and vacant site mediated synapse elimination at developing neuromuscular junctions
title_full_unstemmed Terminal Schwann cell and vacant site mediated synapse elimination at developing neuromuscular junctions
title_short Terminal Schwann cell and vacant site mediated synapse elimination at developing neuromuscular junctions
title_sort terminal schwann cell and vacant site mediated synapse elimination at developing neuromuscular junctions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901572/
https://www.ncbi.nlm.nih.gov/pubmed/31819113
http://dx.doi.org/10.1038/s41598-019-55017-w
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