Cargando…

Distinct roles of nonmuscle myosin II isoforms for establishing tension and elasticity during cell morphodynamics

Nonmuscle myosin II (NM II) is an integral part of essential cellular processes, including adhesion and migration. Mammalian cells express up to three isoforms termed NM IIA, B, and C. We used U2OS cells to create CRISPR/Cas9-based knockouts of all three isoforms and analyzed the phenotypes on homog...

Descripción completa

Detalles Bibliográficos
Autores principales: Weißenbruch, Kai, Grewe, Justin, Hippler, Marc, Fladung, Magdalena, Tremmel, Moritz, Stricker, Kathrin, Schwarz, Ulrich Sebastian, Bastmeyer, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391736/
https://www.ncbi.nlm.nih.gov/pubmed/34374341
http://dx.doi.org/10.7554/eLife.71888
_version_ 1783743344475635712
author Weißenbruch, Kai
Grewe, Justin
Hippler, Marc
Fladung, Magdalena
Tremmel, Moritz
Stricker, Kathrin
Schwarz, Ulrich Sebastian
Bastmeyer, Martin
author_facet Weißenbruch, Kai
Grewe, Justin
Hippler, Marc
Fladung, Magdalena
Tremmel, Moritz
Stricker, Kathrin
Schwarz, Ulrich Sebastian
Bastmeyer, Martin
author_sort Weißenbruch, Kai
collection PubMed
description Nonmuscle myosin II (NM II) is an integral part of essential cellular processes, including adhesion and migration. Mammalian cells express up to three isoforms termed NM IIA, B, and C. We used U2OS cells to create CRISPR/Cas9-based knockouts of all three isoforms and analyzed the phenotypes on homogenously coated surfaces, in collagen gels, and on micropatterned substrates. In contrast to homogenously coated surfaces, a structured environment supports a cellular phenotype with invaginated actin arcs even in the absence of NM IIA-induced contractility. A quantitative shape analysis of cells on micropatterns combined with a scale-bridging mathematical model reveals that NM IIA is essential to build up cellular tension during initial stages of force generation, while NM IIB is necessary to elastically stabilize NM IIA-generated tension. A dynamic cell stretch/release experiment in a three-dimensional scaffold confirms these conclusions and in addition reveals a novel role for NM IIC, namely the ability to establish tensional homeostasis.
format Online
Article
Text
id pubmed-8391736
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-83917362021-08-30 Distinct roles of nonmuscle myosin II isoforms for establishing tension and elasticity during cell morphodynamics Weißenbruch, Kai Grewe, Justin Hippler, Marc Fladung, Magdalena Tremmel, Moritz Stricker, Kathrin Schwarz, Ulrich Sebastian Bastmeyer, Martin eLife Cell Biology Nonmuscle myosin II (NM II) is an integral part of essential cellular processes, including adhesion and migration. Mammalian cells express up to three isoforms termed NM IIA, B, and C. We used U2OS cells to create CRISPR/Cas9-based knockouts of all three isoforms and analyzed the phenotypes on homogenously coated surfaces, in collagen gels, and on micropatterned substrates. In contrast to homogenously coated surfaces, a structured environment supports a cellular phenotype with invaginated actin arcs even in the absence of NM IIA-induced contractility. A quantitative shape analysis of cells on micropatterns combined with a scale-bridging mathematical model reveals that NM IIA is essential to build up cellular tension during initial stages of force generation, while NM IIB is necessary to elastically stabilize NM IIA-generated tension. A dynamic cell stretch/release experiment in a three-dimensional scaffold confirms these conclusions and in addition reveals a novel role for NM IIC, namely the ability to establish tensional homeostasis. eLife Sciences Publications, Ltd 2021-08-10 /pmc/articles/PMC8391736/ /pubmed/34374341 http://dx.doi.org/10.7554/eLife.71888 Text en © 2021, Weißenbruch et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Weißenbruch, Kai
Grewe, Justin
Hippler, Marc
Fladung, Magdalena
Tremmel, Moritz
Stricker, Kathrin
Schwarz, Ulrich Sebastian
Bastmeyer, Martin
Distinct roles of nonmuscle myosin II isoforms for establishing tension and elasticity during cell morphodynamics
title Distinct roles of nonmuscle myosin II isoforms for establishing tension and elasticity during cell morphodynamics
title_full Distinct roles of nonmuscle myosin II isoforms for establishing tension and elasticity during cell morphodynamics
title_fullStr Distinct roles of nonmuscle myosin II isoforms for establishing tension and elasticity during cell morphodynamics
title_full_unstemmed Distinct roles of nonmuscle myosin II isoforms for establishing tension and elasticity during cell morphodynamics
title_short Distinct roles of nonmuscle myosin II isoforms for establishing tension and elasticity during cell morphodynamics
title_sort distinct roles of nonmuscle myosin ii isoforms for establishing tension and elasticity during cell morphodynamics
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391736/
https://www.ncbi.nlm.nih.gov/pubmed/34374341
http://dx.doi.org/10.7554/eLife.71888
work_keys_str_mv AT weißenbruchkai distinctrolesofnonmusclemyosiniiisoformsforestablishingtensionandelasticityduringcellmorphodynamics
AT grewejustin distinctrolesofnonmusclemyosiniiisoformsforestablishingtensionandelasticityduringcellmorphodynamics
AT hipplermarc distinctrolesofnonmusclemyosiniiisoformsforestablishingtensionandelasticityduringcellmorphodynamics
AT fladungmagdalena distinctrolesofnonmusclemyosiniiisoformsforestablishingtensionandelasticityduringcellmorphodynamics
AT tremmelmoritz distinctrolesofnonmusclemyosiniiisoformsforestablishingtensionandelasticityduringcellmorphodynamics
AT strickerkathrin distinctrolesofnonmusclemyosiniiisoformsforestablishingtensionandelasticityduringcellmorphodynamics
AT schwarzulrichsebastian distinctrolesofnonmusclemyosiniiisoformsforestablishingtensionandelasticityduringcellmorphodynamics
AT bastmeyermartin distinctrolesofnonmusclemyosiniiisoformsforestablishingtensionandelasticityduringcellmorphodynamics