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Mechanically patterned neuromuscular junctions-in-a-dish have improved functional maturation

Motor neuron (MN) diseases are progressive disorders resulting from degeneration of neuromuscular junctions (NMJs), which form the connection between MNs and muscle fibers. NMJ-in-a-dish models have been developed to examine human MN-associated dysfunction with disease; however such coculture models...

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Autores principales: Happe, Cassandra L., Tenerelli, Kevin P., Gromova, Anastasia K., Kolb, Frederic, Engler, Adam J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541845/
https://www.ncbi.nlm.nih.gov/pubmed/28495800
http://dx.doi.org/10.1091/mbc.E17-01-0046
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author Happe, Cassandra L.
Tenerelli, Kevin P.
Gromova, Anastasia K.
Kolb, Frederic
Engler, Adam J.
author_facet Happe, Cassandra L.
Tenerelli, Kevin P.
Gromova, Anastasia K.
Kolb, Frederic
Engler, Adam J.
author_sort Happe, Cassandra L.
collection PubMed
description Motor neuron (MN) diseases are progressive disorders resulting from degeneration of neuromuscular junctions (NMJs), which form the connection between MNs and muscle fibers. NMJ-in-a-dish models have been developed to examine human MN-associated dysfunction with disease; however such coculture models have randomly oriented myotubes with immature synapses that contract asynchronously. Mechanically patterned (MP) extracellular matrix with alternating soft and stiff stripes improves current NMJ-in-a-dish models by inducing both mouse and human myoblast durotaxis to stripes where they aligned, differentiated, and fused into patterned myotubes. Compared to conventional culture on rigid substrates or unpatterned hydrogels, MP substrates supported increased differentiation and fusion, significantly larger acetylcholine (ACh) receptor clusters, and increased expression of MuSK and Lrp4, two cell surface receptors required for NMJ formation. Robust contractions were observed when mouse myotubes were stimulated by ACh, with twitch duration and frequency most closely resembling those for mature muscle on MP substrates. Fused myotubes, when cocultured with MNs, were able to form even larger NMJs. Thus MP matrices produce more functionally active NMJs-in-a-dish, which could be used to elucidate disease pathology and facilitate drug discovery.
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spelling pubmed-55418452017-09-22 Mechanically patterned neuromuscular junctions-in-a-dish have improved functional maturation Happe, Cassandra L. Tenerelli, Kevin P. Gromova, Anastasia K. Kolb, Frederic Engler, Adam J. Mol Biol Cell Articles Motor neuron (MN) diseases are progressive disorders resulting from degeneration of neuromuscular junctions (NMJs), which form the connection between MNs and muscle fibers. NMJ-in-a-dish models have been developed to examine human MN-associated dysfunction with disease; however such coculture models have randomly oriented myotubes with immature synapses that contract asynchronously. Mechanically patterned (MP) extracellular matrix with alternating soft and stiff stripes improves current NMJ-in-a-dish models by inducing both mouse and human myoblast durotaxis to stripes where they aligned, differentiated, and fused into patterned myotubes. Compared to conventional culture on rigid substrates or unpatterned hydrogels, MP substrates supported increased differentiation and fusion, significantly larger acetylcholine (ACh) receptor clusters, and increased expression of MuSK and Lrp4, two cell surface receptors required for NMJ formation. Robust contractions were observed when mouse myotubes were stimulated by ACh, with twitch duration and frequency most closely resembling those for mature muscle on MP substrates. Fused myotubes, when cocultured with MNs, were able to form even larger NMJs. Thus MP matrices produce more functionally active NMJs-in-a-dish, which could be used to elucidate disease pathology and facilitate drug discovery. The American Society for Cell Biology 2017-07-07 /pmc/articles/PMC5541845/ /pubmed/28495800 http://dx.doi.org/10.1091/mbc.E17-01-0046 Text en © 2017 Happe et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.
spellingShingle Articles
Happe, Cassandra L.
Tenerelli, Kevin P.
Gromova, Anastasia K.
Kolb, Frederic
Engler, Adam J.
Mechanically patterned neuromuscular junctions-in-a-dish have improved functional maturation
title Mechanically patterned neuromuscular junctions-in-a-dish have improved functional maturation
title_full Mechanically patterned neuromuscular junctions-in-a-dish have improved functional maturation
title_fullStr Mechanically patterned neuromuscular junctions-in-a-dish have improved functional maturation
title_full_unstemmed Mechanically patterned neuromuscular junctions-in-a-dish have improved functional maturation
title_short Mechanically patterned neuromuscular junctions-in-a-dish have improved functional maturation
title_sort mechanically patterned neuromuscular junctions-in-a-dish have improved functional maturation
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541845/
https://www.ncbi.nlm.nih.gov/pubmed/28495800
http://dx.doi.org/10.1091/mbc.E17-01-0046
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