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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...

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Autores principales: Hammers, David W, Hart, Cora C, Matheny, Michael K, Heimsath, Ernest G, Lee, Young il, Hammer, John A, Cheney, Richard E, Sweeney, H Lee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
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.
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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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