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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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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. |
format | Online Article Text |
id | pubmed-6901572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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