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Calponin-3 is critical for coordinated contractility of actin stress fibers

Contractile actomyosin bundles, stress fibers, contribute to morphogenesis, migration, and mechanosensing of non-muscle cells. In addition to actin and non-muscle myosin II (NMII), stress fibers contain a large array of proteins that control their assembly, turnover, and contractility. Calponin-3 (C...

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Autores principales: Ciuba, Katarzyna, Hawkes, William, Tojkander, Sari, Kogan, Konstantin, Engel, Ulrike, Iskratsch, Thomas, Lappalainen, Pekka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281606/
https://www.ncbi.nlm.nih.gov/pubmed/30518778
http://dx.doi.org/10.1038/s41598-018-35948-6
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author Ciuba, Katarzyna
Hawkes, William
Tojkander, Sari
Kogan, Konstantin
Engel, Ulrike
Iskratsch, Thomas
Lappalainen, Pekka
author_facet Ciuba, Katarzyna
Hawkes, William
Tojkander, Sari
Kogan, Konstantin
Engel, Ulrike
Iskratsch, Thomas
Lappalainen, Pekka
author_sort Ciuba, Katarzyna
collection PubMed
description Contractile actomyosin bundles, stress fibers, contribute to morphogenesis, migration, and mechanosensing of non-muscle cells. In addition to actin and non-muscle myosin II (NMII), stress fibers contain a large array of proteins that control their assembly, turnover, and contractility. Calponin-3 (Cnn3) is an actin-binding protein that associates with stress fibers. However, whether Cnn3 promotes stress fiber assembly, or serves as either a positive or negative regulator of their contractility has remained obscure. Here, we applied U2OS osteosarcoma cells as a model system to study the function of Cnn3. We show that Cnn3 localizes to both NMII-containing contractile ventral stress fibers and transverse arcs, as well as to non-contractile dorsal stress fibers that do not contain NMII. Fluorescence-recovery-after-photobleaching experiments revealed that Cnn3 is a dynamic component of stress fibers. Importantly, CRISPR/Cas9 knockout and RNAi knockdown studies demonstrated that Cnn3 is not essential for stress fiber assembly. However, Cnn3 depletion resulted in increased and uncoordinated contractility of stress fibers that often led to breakage of individual actomyosin bundles within the stress fiber network. Collectively these results provide evidence that Cnn3 is dispensable for the assembly of actomyosin bundles, but that it is required for controlling proper contractility of the stress fiber network.
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spelling pubmed-62816062018-12-07 Calponin-3 is critical for coordinated contractility of actin stress fibers Ciuba, Katarzyna Hawkes, William Tojkander, Sari Kogan, Konstantin Engel, Ulrike Iskratsch, Thomas Lappalainen, Pekka Sci Rep Article Contractile actomyosin bundles, stress fibers, contribute to morphogenesis, migration, and mechanosensing of non-muscle cells. In addition to actin and non-muscle myosin II (NMII), stress fibers contain a large array of proteins that control their assembly, turnover, and contractility. Calponin-3 (Cnn3) is an actin-binding protein that associates with stress fibers. However, whether Cnn3 promotes stress fiber assembly, or serves as either a positive or negative regulator of their contractility has remained obscure. Here, we applied U2OS osteosarcoma cells as a model system to study the function of Cnn3. We show that Cnn3 localizes to both NMII-containing contractile ventral stress fibers and transverse arcs, as well as to non-contractile dorsal stress fibers that do not contain NMII. Fluorescence-recovery-after-photobleaching experiments revealed that Cnn3 is a dynamic component of stress fibers. Importantly, CRISPR/Cas9 knockout and RNAi knockdown studies demonstrated that Cnn3 is not essential for stress fiber assembly. However, Cnn3 depletion resulted in increased and uncoordinated contractility of stress fibers that often led to breakage of individual actomyosin bundles within the stress fiber network. Collectively these results provide evidence that Cnn3 is dispensable for the assembly of actomyosin bundles, but that it is required for controlling proper contractility of the stress fiber network. Nature Publishing Group UK 2018-12-05 /pmc/articles/PMC6281606/ /pubmed/30518778 http://dx.doi.org/10.1038/s41598-018-35948-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ciuba, Katarzyna
Hawkes, William
Tojkander, Sari
Kogan, Konstantin
Engel, Ulrike
Iskratsch, Thomas
Lappalainen, Pekka
Calponin-3 is critical for coordinated contractility of actin stress fibers
title Calponin-3 is critical for coordinated contractility of actin stress fibers
title_full Calponin-3 is critical for coordinated contractility of actin stress fibers
title_fullStr Calponin-3 is critical for coordinated contractility of actin stress fibers
title_full_unstemmed Calponin-3 is critical for coordinated contractility of actin stress fibers
title_short Calponin-3 is critical for coordinated contractility of actin stress fibers
title_sort calponin-3 is critical for coordinated contractility of actin stress fibers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281606/
https://www.ncbi.nlm.nih.gov/pubmed/30518778
http://dx.doi.org/10.1038/s41598-018-35948-6
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