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Gaussian curvature dilutes the nuclear lamina, favoring nuclear rupture, especially at high strain rate
Nuclear rupture has long been associated with deficits or defects in lamins, with recent results also indicating a role for actomyosin stress, but key physical determinants of rupture remain unclear. Here, lamin-B filaments stably interact with the nuclear membrane at sites of low Gaussian curvature...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8928808/ https://www.ncbi.nlm.nih.gov/pubmed/35293271 http://dx.doi.org/10.1080/19491034.2022.2045726 |
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author | Pfeifer, Charlotte R. Tobin, Michael P. Cho, Sangkyun Vashisth, Manasvita Dooling, Lawrence J. Vazquez, Lizeth Lopez Ricci-De Lucca, Emma G. Simon, Keiann T. Discher, Dennis E. |
author_facet | Pfeifer, Charlotte R. Tobin, Michael P. Cho, Sangkyun Vashisth, Manasvita Dooling, Lawrence J. Vazquez, Lizeth Lopez Ricci-De Lucca, Emma G. Simon, Keiann T. Discher, Dennis E. |
author_sort | Pfeifer, Charlotte R. |
collection | PubMed |
description | Nuclear rupture has long been associated with deficits or defects in lamins, with recent results also indicating a role for actomyosin stress, but key physical determinants of rupture remain unclear. Here, lamin-B filaments stably interact with the nuclear membrane at sites of low Gaussian curvature yet dilute at high curvature to favor rupture, whereas lamin-A depletion requires high strain-rates. Live-cell imaging of lamin-B1 gene-edited cancer cells is complemented by fixed-cell imaging of rupture in: iPS-derived progeria patients cells, cells within beating chick embryo hearts, and cancer cells with multi-site rupture after migration through small pores. Data fit a model of stiff filaments that detach from a curved surface.Rupture is modestly suppressed by inhibiting myosin-II and by hypotonic stress, which slow the strain-rates. Lamin-A dilution and rupture probability indeed increase above a threshold rate of nuclear pulling. Curvature-sensing mechanisms of proteins at plasma membranes, including Piezo1, might thus apply at nuclear membranes. Summary statement: High nuclear curvature drives lamina dilution and nuclear envelope rupture even when myosin stress is inhibited. Stiff filaments generally dilute from sites of high Gaussian curvature, providing mathematical fits of experiments. |
format | Online Article Text |
id | pubmed-8928808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-89288082022-03-18 Gaussian curvature dilutes the nuclear lamina, favoring nuclear rupture, especially at high strain rate Pfeifer, Charlotte R. Tobin, Michael P. Cho, Sangkyun Vashisth, Manasvita Dooling, Lawrence J. Vazquez, Lizeth Lopez Ricci-De Lucca, Emma G. Simon, Keiann T. Discher, Dennis E. Nucleus Research Paper Nuclear rupture has long been associated with deficits or defects in lamins, with recent results also indicating a role for actomyosin stress, but key physical determinants of rupture remain unclear. Here, lamin-B filaments stably interact with the nuclear membrane at sites of low Gaussian curvature yet dilute at high curvature to favor rupture, whereas lamin-A depletion requires high strain-rates. Live-cell imaging of lamin-B1 gene-edited cancer cells is complemented by fixed-cell imaging of rupture in: iPS-derived progeria patients cells, cells within beating chick embryo hearts, and cancer cells with multi-site rupture after migration through small pores. Data fit a model of stiff filaments that detach from a curved surface.Rupture is modestly suppressed by inhibiting myosin-II and by hypotonic stress, which slow the strain-rates. Lamin-A dilution and rupture probability indeed increase above a threshold rate of nuclear pulling. Curvature-sensing mechanisms of proteins at plasma membranes, including Piezo1, might thus apply at nuclear membranes. Summary statement: High nuclear curvature drives lamina dilution and nuclear envelope rupture even when myosin stress is inhibited. Stiff filaments generally dilute from sites of high Gaussian curvature, providing mathematical fits of experiments. Taylor & Francis 2022-03-16 /pmc/articles/PMC8928808/ /pubmed/35293271 http://dx.doi.org/10.1080/19491034.2022.2045726 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Pfeifer, Charlotte R. Tobin, Michael P. Cho, Sangkyun Vashisth, Manasvita Dooling, Lawrence J. Vazquez, Lizeth Lopez Ricci-De Lucca, Emma G. Simon, Keiann T. Discher, Dennis E. Gaussian curvature dilutes the nuclear lamina, favoring nuclear rupture, especially at high strain rate |
title | Gaussian curvature dilutes the nuclear lamina, favoring nuclear rupture, especially at high strain rate |
title_full | Gaussian curvature dilutes the nuclear lamina, favoring nuclear rupture, especially at high strain rate |
title_fullStr | Gaussian curvature dilutes the nuclear lamina, favoring nuclear rupture, especially at high strain rate |
title_full_unstemmed | Gaussian curvature dilutes the nuclear lamina, favoring nuclear rupture, especially at high strain rate |
title_short | Gaussian curvature dilutes the nuclear lamina, favoring nuclear rupture, especially at high strain rate |
title_sort | gaussian curvature dilutes the nuclear lamina, favoring nuclear rupture, especially at high strain rate |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8928808/ https://www.ncbi.nlm.nih.gov/pubmed/35293271 http://dx.doi.org/10.1080/19491034.2022.2045726 |
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