Cell elasticity is regulated by the tropomyosin isoform composition of the actin cytoskeleton.

The actin cytoskeleton is the primary polymer system within cells responsible for regulating cellular stiffness. While various actin binding proteins regulate the organization and dynamics of the actin cytoskeleton, the proteins responsible for regulating the mechanical properties of cells are still...

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Main Authors: Iman Jalilian, Celine Heu, Hong Cheng, Hannah Freittag, Melissa Desouza, Justine R Stehn, Nicole S Bryce, Renee M Whan, Edna C Hardeman, Thomas Fath, Galina Schevzov, Peter W Gunning
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0126214
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author Iman Jalilian
Celine Heu
Hong Cheng
Hannah Freittag
Melissa Desouza
Justine R Stehn
Nicole S Bryce
Renee M Whan
Edna C Hardeman
Thomas Fath
Galina Schevzov
Peter W Gunning
author_facet Iman Jalilian
Celine Heu
Hong Cheng
Hannah Freittag
Melissa Desouza
Justine R Stehn
Nicole S Bryce
Renee M Whan
Edna C Hardeman
Thomas Fath
Galina Schevzov
Peter W Gunning
author_sort Iman Jalilian
collection DOAJ
description The actin cytoskeleton is the primary polymer system within cells responsible for regulating cellular stiffness. While various actin binding proteins regulate the organization and dynamics of the actin cytoskeleton, the proteins responsible for regulating the mechanical properties of cells are still not fully understood. In the present study, we have addressed the significance of the actin associated protein, tropomyosin (Tpm), in influencing the mechanical properties of cells. Tpms belong to a multi-gene family that form a co-polymer with actin filaments and differentially regulate actin filament stability, function and organization. Tpm isoform expression is highly regulated and together with the ability to sort to specific intracellular sites, result in the generation of distinct Tpm isoform-containing actin filament populations. Nanomechanical measurements conducted with an Atomic Force Microscope using indentation in Peak Force Tapping in indentation/ramping mode, demonstrated that Tpm impacts on cell stiffness and the observed effect occurred in a Tpm isoform-specific manner. Quantitative analysis of the cellular filamentous actin (F-actin) pool conducted both biochemically and with the use of a linear detection algorithm to evaluate actin structures revealed that an altered F-actin pool does not absolutely predict changes in cell stiffness. Inhibition of non-muscle myosin II revealed that intracellular tension generated by myosin II is required for the observed increase in cell stiffness. Lastly, we show that the observed increase in cell stiffness is partially recapitulated in vivo as detected in epididymal fat pads isolated from a Tpm3.1 transgenic mouse line. Together these data are consistent with a role for Tpm in regulating cell stiffness via the generation of specific populations of Tpm isoform-containing actin filaments.
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spelling doaj.art-c03859392a5f4daa968f0b45f919ec942022-12-21T21:31:39ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01105e012621410.1371/journal.pone.0126214Cell elasticity is regulated by the tropomyosin isoform composition of the actin cytoskeleton.Iman JalilianCeline HeuHong ChengHannah FreittagMelissa DesouzaJustine R StehnNicole S BryceRenee M WhanEdna C HardemanThomas FathGalina SchevzovPeter W GunningThe actin cytoskeleton is the primary polymer system within cells responsible for regulating cellular stiffness. While various actin binding proteins regulate the organization and dynamics of the actin cytoskeleton, the proteins responsible for regulating the mechanical properties of cells are still not fully understood. In the present study, we have addressed the significance of the actin associated protein, tropomyosin (Tpm), in influencing the mechanical properties of cells. Tpms belong to a multi-gene family that form a co-polymer with actin filaments and differentially regulate actin filament stability, function and organization. Tpm isoform expression is highly regulated and together with the ability to sort to specific intracellular sites, result in the generation of distinct Tpm isoform-containing actin filament populations. Nanomechanical measurements conducted with an Atomic Force Microscope using indentation in Peak Force Tapping in indentation/ramping mode, demonstrated that Tpm impacts on cell stiffness and the observed effect occurred in a Tpm isoform-specific manner. Quantitative analysis of the cellular filamentous actin (F-actin) pool conducted both biochemically and with the use of a linear detection algorithm to evaluate actin structures revealed that an altered F-actin pool does not absolutely predict changes in cell stiffness. Inhibition of non-muscle myosin II revealed that intracellular tension generated by myosin II is required for the observed increase in cell stiffness. Lastly, we show that the observed increase in cell stiffness is partially recapitulated in vivo as detected in epididymal fat pads isolated from a Tpm3.1 transgenic mouse line. Together these data are consistent with a role for Tpm in regulating cell stiffness via the generation of specific populations of Tpm isoform-containing actin filaments.https://doi.org/10.1371/journal.pone.0126214
spellingShingle Iman Jalilian
Celine Heu
Hong Cheng
Hannah Freittag
Melissa Desouza
Justine R Stehn
Nicole S Bryce
Renee M Whan
Edna C Hardeman
Thomas Fath
Galina Schevzov
Peter W Gunning
Cell elasticity is regulated by the tropomyosin isoform composition of the actin cytoskeleton.
PLoS ONE
title Cell elasticity is regulated by the tropomyosin isoform composition of the actin cytoskeleton.
title_full Cell elasticity is regulated by the tropomyosin isoform composition of the actin cytoskeleton.
title_fullStr Cell elasticity is regulated by the tropomyosin isoform composition of the actin cytoskeleton.
title_full_unstemmed Cell elasticity is regulated by the tropomyosin isoform composition of the actin cytoskeleton.
title_short Cell elasticity is regulated by the tropomyosin isoform composition of the actin cytoskeleton.
title_sort cell elasticity is regulated by the tropomyosin isoform composition of the actin cytoskeleton
url https://doi.org/10.1371/journal.pone.0126214
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