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Creating stem cell‐derived neuromuscular junctions in vitro
Recent development of novel therapies has improved mobility and quality of life for people suffering from inheritable neuromuscular disorders. Despite this progress, the majority of neuromuscular disorders are still incurable, in part due to a lack of predictive models of neuromuscular junction (NMJ...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292444/ https://www.ncbi.nlm.nih.gov/pubmed/34328673 http://dx.doi.org/10.1002/mus.27360 |
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author | Luttrell, Shawn M. Smith, Alec S. T. Mack, David L. |
author_facet | Luttrell, Shawn M. Smith, Alec S. T. Mack, David L. |
author_sort | Luttrell, Shawn M. |
collection | PubMed |
description | Recent development of novel therapies has improved mobility and quality of life for people suffering from inheritable neuromuscular disorders. Despite this progress, the majority of neuromuscular disorders are still incurable, in part due to a lack of predictive models of neuromuscular junction (NMJ) breakdown. Improvement of predictive models of a human NMJ would be transformative in terms of expanding our understanding of the mechanisms that underpin development, maintenance, and disease, and as a testbed with which to evaluate novel therapeutics. Induced pluripotent stem cells (iPSCs) are emerging as a clinically relevant and non‐invasive cell source to create human NMJs to study synaptic development and maturation, as well as disease modeling and drug discovery. This review will highlight the recent advances and remaining challenges to generating an NMJ capable of eliciting contraction of stem cell‐derived skeletal muscle in vitro. We explore the advantages and shortcomings of traditional NMJ culturing platforms, as well as the pioneering technologies and novel, biomimetic culturing systems currently in use to guide development and maturation of the neuromuscular synapse and extracellular microenvironment. Then, we will explore how this NMJ‐in‐a‐dish can be used to study normal assembly and function of the efferent portion of the neuromuscular arc, and how neuromuscular disease‐causing mutations disrupt structure, signaling, and function. |
format | Online Article Text |
id | pubmed-9292444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92924442022-07-20 Creating stem cell‐derived neuromuscular junctions in vitro Luttrell, Shawn M. Smith, Alec S. T. Mack, David L. Muscle Nerve Invited Review Recent development of novel therapies has improved mobility and quality of life for people suffering from inheritable neuromuscular disorders. Despite this progress, the majority of neuromuscular disorders are still incurable, in part due to a lack of predictive models of neuromuscular junction (NMJ) breakdown. Improvement of predictive models of a human NMJ would be transformative in terms of expanding our understanding of the mechanisms that underpin development, maintenance, and disease, and as a testbed with which to evaluate novel therapeutics. Induced pluripotent stem cells (iPSCs) are emerging as a clinically relevant and non‐invasive cell source to create human NMJs to study synaptic development and maturation, as well as disease modeling and drug discovery. This review will highlight the recent advances and remaining challenges to generating an NMJ capable of eliciting contraction of stem cell‐derived skeletal muscle in vitro. We explore the advantages and shortcomings of traditional NMJ culturing platforms, as well as the pioneering technologies and novel, biomimetic culturing systems currently in use to guide development and maturation of the neuromuscular synapse and extracellular microenvironment. Then, we will explore how this NMJ‐in‐a‐dish can be used to study normal assembly and function of the efferent portion of the neuromuscular arc, and how neuromuscular disease‐causing mutations disrupt structure, signaling, and function. John Wiley & Sons, Inc. 2021-07-30 2021-10 /pmc/articles/PMC9292444/ /pubmed/34328673 http://dx.doi.org/10.1002/mus.27360 Text en © 2021 The Authors. Muscle & Nerve published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Invited Review Luttrell, Shawn M. Smith, Alec S. T. Mack, David L. Creating stem cell‐derived neuromuscular junctions in vitro |
title | Creating stem cell‐derived neuromuscular junctions in vitro |
title_full | Creating stem cell‐derived neuromuscular junctions in vitro |
title_fullStr | Creating stem cell‐derived neuromuscular junctions in vitro |
title_full_unstemmed | Creating stem cell‐derived neuromuscular junctions in vitro |
title_short | Creating stem cell‐derived neuromuscular junctions in vitro |
title_sort | creating stem cell‐derived neuromuscular junctions in vitro |
topic | Invited Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292444/ https://www.ncbi.nlm.nih.gov/pubmed/34328673 http://dx.doi.org/10.1002/mus.27360 |
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