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Nuclear lamin A/C harnesses the perinuclear apical actin cables to protect nuclear morphology

The distinct spatial architecture of the apical actin cables (or actin cap) facilitates rapid biophysical signaling between extracellular mechanical stimuli and intracellular responses, including nuclear shaping, cytoskeletal remodeling, and the mechanotransduction of external forces into biochemica...

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Autores principales: Kim, Jeong-Ki, Louhghalam, Arghavan, Lee, Geonhui, Schafer, Benjamin W., Wirtz, Denis, Kim, Dong-Hwee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5730574/
https://www.ncbi.nlm.nih.gov/pubmed/29242553
http://dx.doi.org/10.1038/s41467-017-02217-5
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author Kim, Jeong-Ki
Louhghalam, Arghavan
Lee, Geonhui
Schafer, Benjamin W.
Wirtz, Denis
Kim, Dong-Hwee
author_facet Kim, Jeong-Ki
Louhghalam, Arghavan
Lee, Geonhui
Schafer, Benjamin W.
Wirtz, Denis
Kim, Dong-Hwee
author_sort Kim, Jeong-Ki
collection PubMed
description The distinct spatial architecture of the apical actin cables (or actin cap) facilitates rapid biophysical signaling between extracellular mechanical stimuli and intracellular responses, including nuclear shaping, cytoskeletal remodeling, and the mechanotransduction of external forces into biochemical signals. These functions are abrogated in lamin A/C-deficient mouse embryonic fibroblasts that recapitulate the defective nuclear organization of laminopathies, featuring disruption of the actin cap. However, how nuclear lamin A/C mediates the ability of the actin cap to regulate nuclear morphology remains unclear. Here, we show that lamin A/C expressing cells can form an actin cap to resist nuclear deformation in response to physiological mechanical stresses. This study reveals how the nuclear lamin A/C-mediated formation of the perinuclear apical actin cables protects the nuclear structural integrity from extracellular physical disturbances. Our findings highlight the role of the physical interactions between the cytoskeletal network and the nucleus in cellular mechanical homeostasis.
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spelling pubmed-57305742017-12-18 Nuclear lamin A/C harnesses the perinuclear apical actin cables to protect nuclear morphology Kim, Jeong-Ki Louhghalam, Arghavan Lee, Geonhui Schafer, Benjamin W. Wirtz, Denis Kim, Dong-Hwee Nat Commun Article The distinct spatial architecture of the apical actin cables (or actin cap) facilitates rapid biophysical signaling between extracellular mechanical stimuli and intracellular responses, including nuclear shaping, cytoskeletal remodeling, and the mechanotransduction of external forces into biochemical signals. These functions are abrogated in lamin A/C-deficient mouse embryonic fibroblasts that recapitulate the defective nuclear organization of laminopathies, featuring disruption of the actin cap. However, how nuclear lamin A/C mediates the ability of the actin cap to regulate nuclear morphology remains unclear. Here, we show that lamin A/C expressing cells can form an actin cap to resist nuclear deformation in response to physiological mechanical stresses. This study reveals how the nuclear lamin A/C-mediated formation of the perinuclear apical actin cables protects the nuclear structural integrity from extracellular physical disturbances. Our findings highlight the role of the physical interactions between the cytoskeletal network and the nucleus in cellular mechanical homeostasis. Nature Publishing Group UK 2017-12-14 /pmc/articles/PMC5730574/ /pubmed/29242553 http://dx.doi.org/10.1038/s41467-017-02217-5 Text en © The Author(s) 2017 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
Kim, Jeong-Ki
Louhghalam, Arghavan
Lee, Geonhui
Schafer, Benjamin W.
Wirtz, Denis
Kim, Dong-Hwee
Nuclear lamin A/C harnesses the perinuclear apical actin cables to protect nuclear morphology
title Nuclear lamin A/C harnesses the perinuclear apical actin cables to protect nuclear morphology
title_full Nuclear lamin A/C harnesses the perinuclear apical actin cables to protect nuclear morphology
title_fullStr Nuclear lamin A/C harnesses the perinuclear apical actin cables to protect nuclear morphology
title_full_unstemmed Nuclear lamin A/C harnesses the perinuclear apical actin cables to protect nuclear morphology
title_short Nuclear lamin A/C harnesses the perinuclear apical actin cables to protect nuclear morphology
title_sort nuclear lamin a/c harnesses the perinuclear apical actin cables to protect nuclear morphology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5730574/
https://www.ncbi.nlm.nih.gov/pubmed/29242553
http://dx.doi.org/10.1038/s41467-017-02217-5
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