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Muscle-specific stress fibers give rise to sarcomeres in cardiomyocytes

The sarcomere is the contractile unit within cardiomyocytes driving heart muscle contraction. We sought to test the mechanisms regulating actin and myosin filament assembly during sarcomere formation. Therefore, we developed an assay using human cardiomyocytes to monitor sarcomere assembly. We repor...

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Autores principales: Fenix, Aidan M, Neininger, Abigail C, Taneja, Nilay, Hyde, Karren, Visetsouk, Mike R, Garde, Ryan J, Liu, Baohong, Nixon, Benjamin R, Manalo, Annabelle E, Becker, Jason R, Crawley, Scott W, Bader, David M, Tyska, Matthew J, Liu, Qi, Gutzman, Jennifer H, Burnette, Dylan T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307863/
https://www.ncbi.nlm.nih.gov/pubmed/30540249
http://dx.doi.org/10.7554/eLife.42144
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author Fenix, Aidan M
Neininger, Abigail C
Taneja, Nilay
Hyde, Karren
Visetsouk, Mike R
Garde, Ryan J
Liu, Baohong
Nixon, Benjamin R
Manalo, Annabelle E
Becker, Jason R
Crawley, Scott W
Bader, David M
Tyska, Matthew J
Liu, Qi
Gutzman, Jennifer H
Burnette, Dylan T
author_facet Fenix, Aidan M
Neininger, Abigail C
Taneja, Nilay
Hyde, Karren
Visetsouk, Mike R
Garde, Ryan J
Liu, Baohong
Nixon, Benjamin R
Manalo, Annabelle E
Becker, Jason R
Crawley, Scott W
Bader, David M
Tyska, Matthew J
Liu, Qi
Gutzman, Jennifer H
Burnette, Dylan T
author_sort Fenix, Aidan M
collection PubMed
description The sarcomere is the contractile unit within cardiomyocytes driving heart muscle contraction. We sought to test the mechanisms regulating actin and myosin filament assembly during sarcomere formation. Therefore, we developed an assay using human cardiomyocytes to monitor sarcomere assembly. We report a population of muscle stress fibers, similar to actin arcs in non-muscle cells, which are essential sarcomere precursors. We show sarcomeric actin filaments arise directly from muscle stress fibers. This requires formins (e.g., FHOD3), non-muscle myosin IIA and non-muscle myosin IIB. Furthermore, we show short cardiac myosin II filaments grow to form ~1.5 μm long filaments that then ‘stitch’ together to form the stack of filaments at the core of the sarcomere (i.e., the A-band). A-band assembly is dependent on the proper organization of actin filaments and, as such, is also dependent on FHOD3 and myosin IIB. We use this experimental paradigm to present evidence for a unifying model of sarcomere assembly.
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spelling pubmed-63078632019-01-02 Muscle-specific stress fibers give rise to sarcomeres in cardiomyocytes Fenix, Aidan M Neininger, Abigail C Taneja, Nilay Hyde, Karren Visetsouk, Mike R Garde, Ryan J Liu, Baohong Nixon, Benjamin R Manalo, Annabelle E Becker, Jason R Crawley, Scott W Bader, David M Tyska, Matthew J Liu, Qi Gutzman, Jennifer H Burnette, Dylan T eLife Cell Biology The sarcomere is the contractile unit within cardiomyocytes driving heart muscle contraction. We sought to test the mechanisms regulating actin and myosin filament assembly during sarcomere formation. Therefore, we developed an assay using human cardiomyocytes to monitor sarcomere assembly. We report a population of muscle stress fibers, similar to actin arcs in non-muscle cells, which are essential sarcomere precursors. We show sarcomeric actin filaments arise directly from muscle stress fibers. This requires formins (e.g., FHOD3), non-muscle myosin IIA and non-muscle myosin IIB. Furthermore, we show short cardiac myosin II filaments grow to form ~1.5 μm long filaments that then ‘stitch’ together to form the stack of filaments at the core of the sarcomere (i.e., the A-band). A-band assembly is dependent on the proper organization of actin filaments and, as such, is also dependent on FHOD3 and myosin IIB. We use this experimental paradigm to present evidence for a unifying model of sarcomere assembly. eLife Sciences Publications, Ltd 2018-12-12 /pmc/articles/PMC6307863/ /pubmed/30540249 http://dx.doi.org/10.7554/eLife.42144 Text en © 2018, Fenix et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Fenix, Aidan M
Neininger, Abigail C
Taneja, Nilay
Hyde, Karren
Visetsouk, Mike R
Garde, Ryan J
Liu, Baohong
Nixon, Benjamin R
Manalo, Annabelle E
Becker, Jason R
Crawley, Scott W
Bader, David M
Tyska, Matthew J
Liu, Qi
Gutzman, Jennifer H
Burnette, Dylan T
Muscle-specific stress fibers give rise to sarcomeres in cardiomyocytes
title Muscle-specific stress fibers give rise to sarcomeres in cardiomyocytes
title_full Muscle-specific stress fibers give rise to sarcomeres in cardiomyocytes
title_fullStr Muscle-specific stress fibers give rise to sarcomeres in cardiomyocytes
title_full_unstemmed Muscle-specific stress fibers give rise to sarcomeres in cardiomyocytes
title_short Muscle-specific stress fibers give rise to sarcomeres in cardiomyocytes
title_sort muscle-specific stress fibers give rise to sarcomeres in cardiomyocytes
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307863/
https://www.ncbi.nlm.nih.gov/pubmed/30540249
http://dx.doi.org/10.7554/eLife.42144
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