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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Main Authors: Aidan M Fenix, Abigail C Neininger, Nilay Taneja, Karren Hyde, Mike R Visetsouk, Ryan J Garde, Baohong Liu, Benjamin R Nixon, Annabelle E Manalo, Jason R Becker, Scott W Crawley, David M Bader, Matthew J Tyska, Qi Liu, Jennifer H Gutzman, Dylan T Burnette
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2018-12-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/42144
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spelling doaj-41df8305132b4d9e831a0d1f118408422021-05-05T16:21:04ZengeLife Sciences Publications LtdeLife2050-084X2018-12-01710.7554/eLife.42144Muscle-specific stress fibers give rise to sarcomeres in cardiomyocytesAidan M Fenix0Abigail C Neininger1Nilay Taneja2Karren Hyde3Mike R Visetsouk4Ryan J Garde5Baohong Liu6Benjamin R Nixon7https://orcid.org/0000-0003-1840-0179Annabelle E Manalo8Jason R Becker9https://orcid.org/0000-0002-2107-8179Scott W Crawley10David M Bader11Matthew J Tyska12Qi Liu13Jennifer H Gutzman14https://orcid.org/0000-0002-7725-6923Dylan T Burnette15https://orcid.org/0000-0002-2571-7038Department of Cell and Developmental Biology, Vanderbilt University, Nashville, United StatesDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, United StatesDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, United StatesDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, United StatesDepartment of Biological Sciences, Cell and Molecular Biology, University of Wisconsin Milwaukee, Milwaukee, United StatesDepartment of Biological Sciences, Cell and Molecular Biology, University of Wisconsin Milwaukee, Milwaukee, United StatesDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, United StatesDepartment of Medicine, Vanderbilt University Medical Center, Nashville, United StatesDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, United StatesDepartment of Medicine, Vanderbilt University Medical Center, Nashville, United StatesDepartment of Biological Sciences, The University of Toledo, Toledo, United StatesDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, United StatesDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, United StatesDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, United StatesDepartment of Biological Sciences, Cell and Molecular Biology, University of Wisconsin Milwaukee, Milwaukee, United StatesDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, United StatesThe 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.https://elifesciences.org/articles/42144cardiomyocytesactinmyosinforminssarcomeres
collection DOAJ
language English
format Article
sources DOAJ
author Aidan M Fenix
Abigail C Neininger
Nilay Taneja
Karren Hyde
Mike R Visetsouk
Ryan J Garde
Baohong Liu
Benjamin R Nixon
Annabelle E Manalo
Jason R Becker
Scott W Crawley
David M Bader
Matthew J Tyska
Qi Liu
Jennifer H Gutzman
Dylan T Burnette
spellingShingle Aidan M Fenix
Abigail C Neininger
Nilay Taneja
Karren Hyde
Mike R Visetsouk
Ryan J Garde
Baohong Liu
Benjamin R Nixon
Annabelle E Manalo
Jason R Becker
Scott W Crawley
David M Bader
Matthew J Tyska
Qi Liu
Jennifer H Gutzman
Dylan T Burnette
Muscle-specific stress fibers give rise to sarcomeres in cardiomyocytes
eLife
cardiomyocytes
actin
myosin
formins
sarcomeres
author_facet Aidan M Fenix
Abigail C Neininger
Nilay Taneja
Karren Hyde
Mike R Visetsouk
Ryan J Garde
Baohong Liu
Benjamin R Nixon
Annabelle E Manalo
Jason R Becker
Scott W Crawley
David M Bader
Matthew J Tyska
Qi Liu
Jennifer H Gutzman
Dylan T Burnette
author_sort Aidan M Fenix
title Muscle-specific stress fibers give rise to sarcomeres in cardiomyocytes
title_short 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_sort muscle-specific stress fibers give rise to sarcomeres in cardiomyocytes
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2018-12-01
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.
topic cardiomyocytes
actin
myosin
formins
sarcomeres
url https://elifesciences.org/articles/42144
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