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Spatial distribution of lamin A/C determines nuclear stiffness and stress-mediated deformation

While diverse cellular components have been identified as mechanotransduction elements, the deformation of the nucleus itself is a critical mechanosensory mechanism, implying that nuclear stiffness is essential in determining responses to intracellular and extracellular stresses. Although the nuclea...

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Autores principales: Srivastava, Luv Kishore, Ju, Zhaoping, Ghagre, Ajinkya, Ehrlicher, Allen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186481/
https://www.ncbi.nlm.nih.gov/pubmed/34028539
http://dx.doi.org/10.1242/jcs.248559
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author Srivastava, Luv Kishore
Ju, Zhaoping
Ghagre, Ajinkya
Ehrlicher, Allen J.
author_facet Srivastava, Luv Kishore
Ju, Zhaoping
Ghagre, Ajinkya
Ehrlicher, Allen J.
author_sort Srivastava, Luv Kishore
collection PubMed
description While diverse cellular components have been identified as mechanotransduction elements, the deformation of the nucleus itself is a critical mechanosensory mechanism, implying that nuclear stiffness is essential in determining responses to intracellular and extracellular stresses. Although the nuclear membrane protein lamin A/C is known to contribute to nuclear stiffness, bulk moduli of nuclei have not been reported for various levels of lamin A/C. Here, we measure the nuclear bulk moduli as a function of lamin A/C expression and applied osmotic stress, revealing a linear dependence within the range of 2–4 MPa. We also find that the nuclear compression is anisotropic, with the vertical axis of the nucleus being more compliant than the minor and major axes in the substrate plane. We then related the spatial distribution of lamin A/C with submicron 3D nuclear envelope deformation, revealing that local areas of the nuclear envelope with higher density of lamin A/C have correspondingly lower local deformations. These findings describe the complex dispersion of nuclear deformations as a function of lamin A/C expression and distribution, implicating a lamin A/C role in mechanotransduction. This article has an associated First Person interview with the first author of the paper.
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spelling pubmed-81864812021-06-16 Spatial distribution of lamin A/C determines nuclear stiffness and stress-mediated deformation Srivastava, Luv Kishore Ju, Zhaoping Ghagre, Ajinkya Ehrlicher, Allen J. J Cell Sci Short Report While diverse cellular components have been identified as mechanotransduction elements, the deformation of the nucleus itself is a critical mechanosensory mechanism, implying that nuclear stiffness is essential in determining responses to intracellular and extracellular stresses. Although the nuclear membrane protein lamin A/C is known to contribute to nuclear stiffness, bulk moduli of nuclei have not been reported for various levels of lamin A/C. Here, we measure the nuclear bulk moduli as a function of lamin A/C expression and applied osmotic stress, revealing a linear dependence within the range of 2–4 MPa. We also find that the nuclear compression is anisotropic, with the vertical axis of the nucleus being more compliant than the minor and major axes in the substrate plane. We then related the spatial distribution of lamin A/C with submicron 3D nuclear envelope deformation, revealing that local areas of the nuclear envelope with higher density of lamin A/C have correspondingly lower local deformations. These findings describe the complex dispersion of nuclear deformations as a function of lamin A/C expression and distribution, implicating a lamin A/C role in mechanotransduction. This article has an associated First Person interview with the first author of the paper. The Company of Biologists Ltd 2021-05-24 /pmc/articles/PMC8186481/ /pubmed/34028539 http://dx.doi.org/10.1242/jcs.248559 Text en © 2021. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Short Report
Srivastava, Luv Kishore
Ju, Zhaoping
Ghagre, Ajinkya
Ehrlicher, Allen J.
Spatial distribution of lamin A/C determines nuclear stiffness and stress-mediated deformation
title Spatial distribution of lamin A/C determines nuclear stiffness and stress-mediated deformation
title_full Spatial distribution of lamin A/C determines nuclear stiffness and stress-mediated deformation
title_fullStr Spatial distribution of lamin A/C determines nuclear stiffness and stress-mediated deformation
title_full_unstemmed Spatial distribution of lamin A/C determines nuclear stiffness and stress-mediated deformation
title_short Spatial distribution of lamin A/C determines nuclear stiffness and stress-mediated deformation
title_sort spatial distribution of lamin a/c determines nuclear stiffness and stress-mediated deformation
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186481/
https://www.ncbi.nlm.nih.gov/pubmed/34028539
http://dx.doi.org/10.1242/jcs.248559
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