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Filopodia powered by class x myosin promote fusion of mammalian myoblasts
Skeletal muscle fibers are multinucleated cellular giants formed by the fusion of mononuclear myoblasts. Several molecules involved in myoblast fusion have been discovered, and finger-like projections coincident with myoblast fusion have also been implicated in the fusion process. The role of these...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8500716/ https://www.ncbi.nlm.nih.gov/pubmed/34519272 http://dx.doi.org/10.7554/eLife.72419 |
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author | Hammers, David W Hart, Cora C Matheny, Michael K Heimsath, Ernest G Lee, Young il Hammer, John A Cheney, Richard E Sweeney, H Lee |
author_facet | Hammers, David W Hart, Cora C Matheny, Michael K Heimsath, Ernest G Lee, Young il Hammer, John A Cheney, Richard E Sweeney, H Lee |
author_sort | Hammers, David W |
collection | PubMed |
description | Skeletal muscle fibers are multinucleated cellular giants formed by the fusion of mononuclear myoblasts. Several molecules involved in myoblast fusion have been discovered, and finger-like projections coincident with myoblast fusion have also been implicated in the fusion process. The role of these cellular projections in muscle cell fusion was investigated herein. We demonstrate that these projections are filopodia generated by class X myosin (Myo10), an unconventional myosin motor protein specialized for filopodia. We further show that Myo10 is highly expressed by differentiating myoblasts, and Myo10 ablation inhibits both filopodia formation and myoblast fusion in vitro. In vivo, Myo10 labels regenerating muscle fibers associated with Duchenne muscular dystrophy and acute muscle injury. In mice, conditional loss of Myo10 from muscle-resident stem cells, known as satellite cells, severely impairs postnatal muscle regeneration. Furthermore, the muscle fusion proteins Myomaker and Myomixer are detected in myoblast filopodia. These data demonstrate that Myo10-driven filopodia facilitate multinucleated mammalian muscle formation. |
format | Online Article Text |
id | pubmed-8500716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-85007162021-10-12 Filopodia powered by class x myosin promote fusion of mammalian myoblasts Hammers, David W Hart, Cora C Matheny, Michael K Heimsath, Ernest G Lee, Young il Hammer, John A Cheney, Richard E Sweeney, H Lee eLife Cell Biology Skeletal muscle fibers are multinucleated cellular giants formed by the fusion of mononuclear myoblasts. Several molecules involved in myoblast fusion have been discovered, and finger-like projections coincident with myoblast fusion have also been implicated in the fusion process. The role of these cellular projections in muscle cell fusion was investigated herein. We demonstrate that these projections are filopodia generated by class X myosin (Myo10), an unconventional myosin motor protein specialized for filopodia. We further show that Myo10 is highly expressed by differentiating myoblasts, and Myo10 ablation inhibits both filopodia formation and myoblast fusion in vitro. In vivo, Myo10 labels regenerating muscle fibers associated with Duchenne muscular dystrophy and acute muscle injury. In mice, conditional loss of Myo10 from muscle-resident stem cells, known as satellite cells, severely impairs postnatal muscle regeneration. Furthermore, the muscle fusion proteins Myomaker and Myomixer are detected in myoblast filopodia. These data demonstrate that Myo10-driven filopodia facilitate multinucleated mammalian muscle formation. eLife Sciences Publications, Ltd 2021-09-14 /pmc/articles/PMC8500716/ /pubmed/34519272 http://dx.doi.org/10.7554/eLife.72419 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (https://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Cell Biology Hammers, David W Hart, Cora C Matheny, Michael K Heimsath, Ernest G Lee, Young il Hammer, John A Cheney, Richard E Sweeney, H Lee Filopodia powered by class x myosin promote fusion of mammalian myoblasts |
title | Filopodia powered by class x myosin promote fusion of mammalian myoblasts |
title_full | Filopodia powered by class x myosin promote fusion of mammalian myoblasts |
title_fullStr | Filopodia powered by class x myosin promote fusion of mammalian myoblasts |
title_full_unstemmed | Filopodia powered by class x myosin promote fusion of mammalian myoblasts |
title_short | Filopodia powered by class x myosin promote fusion of mammalian myoblasts |
title_sort | filopodia powered by class x myosin promote fusion of mammalian myoblasts |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8500716/ https://www.ncbi.nlm.nih.gov/pubmed/34519272 http://dx.doi.org/10.7554/eLife.72419 |
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