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A Ca(2+)-Mediated Switch of Epiplakin from a Diffuse to Keratin-Bound State Affects Keratin Dynamics
Keratins exert important structural but also cytoprotective functions. They have to be adaptable to support cellular homeostasis. Epiplakin (EPPK1) has been shown to decorate keratin filaments in epithelial cells and to play a protective role under stress, but the mechanism is still unclear. Using l...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563781/ https://www.ncbi.nlm.nih.gov/pubmed/36231039 http://dx.doi.org/10.3390/cells11193077 |
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author | Ratajczyk, Sonia Drexler, Corinne Windoffer, Reinhard Leube, Rudolf E. Fuchs, Peter |
author_facet | Ratajczyk, Sonia Drexler, Corinne Windoffer, Reinhard Leube, Rudolf E. Fuchs, Peter |
author_sort | Ratajczyk, Sonia |
collection | PubMed |
description | Keratins exert important structural but also cytoprotective functions. They have to be adaptable to support cellular homeostasis. Epiplakin (EPPK1) has been shown to decorate keratin filaments in epithelial cells and to play a protective role under stress, but the mechanism is still unclear. Using live-cell imaging of epithelial cells expressing fluorescently tagged EPPK1 and keratin, we report here an unexpected dynamic behavior of EPPK1 upon stress. EPPK1 was diffusely distributed throughout the cytoplasm and not associated with keratin filaments in living cells under standard culture conditions. However, ER-, oxidative and UV-stress, as well as cell fixation, induced a rapid association of EPPK1 with keratin filaments. This re-localization of EPPK1 was reversible and dependent on the elevation of cytoplasmic Ca(2+) levels. Moreover, keratin filament association of EPPK1 led to significantly reduced keratin dynamics. Thus, we propose that EPPK1 stabilizes the keratin network in stress conditions, which involve increased cytoplasmic Ca(2+). |
format | Online Article Text |
id | pubmed-9563781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95637812022-10-15 A Ca(2+)-Mediated Switch of Epiplakin from a Diffuse to Keratin-Bound State Affects Keratin Dynamics Ratajczyk, Sonia Drexler, Corinne Windoffer, Reinhard Leube, Rudolf E. Fuchs, Peter Cells Communication Keratins exert important structural but also cytoprotective functions. They have to be adaptable to support cellular homeostasis. Epiplakin (EPPK1) has been shown to decorate keratin filaments in epithelial cells and to play a protective role under stress, but the mechanism is still unclear. Using live-cell imaging of epithelial cells expressing fluorescently tagged EPPK1 and keratin, we report here an unexpected dynamic behavior of EPPK1 upon stress. EPPK1 was diffusely distributed throughout the cytoplasm and not associated with keratin filaments in living cells under standard culture conditions. However, ER-, oxidative and UV-stress, as well as cell fixation, induced a rapid association of EPPK1 with keratin filaments. This re-localization of EPPK1 was reversible and dependent on the elevation of cytoplasmic Ca(2+) levels. Moreover, keratin filament association of EPPK1 led to significantly reduced keratin dynamics. Thus, we propose that EPPK1 stabilizes the keratin network in stress conditions, which involve increased cytoplasmic Ca(2+). MDPI 2022-09-30 /pmc/articles/PMC9563781/ /pubmed/36231039 http://dx.doi.org/10.3390/cells11193077 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Ratajczyk, Sonia Drexler, Corinne Windoffer, Reinhard Leube, Rudolf E. Fuchs, Peter A Ca(2+)-Mediated Switch of Epiplakin from a Diffuse to Keratin-Bound State Affects Keratin Dynamics |
title | A Ca(2+)-Mediated Switch of Epiplakin from a Diffuse to Keratin-Bound State Affects Keratin Dynamics |
title_full | A Ca(2+)-Mediated Switch of Epiplakin from a Diffuse to Keratin-Bound State Affects Keratin Dynamics |
title_fullStr | A Ca(2+)-Mediated Switch of Epiplakin from a Diffuse to Keratin-Bound State Affects Keratin Dynamics |
title_full_unstemmed | A Ca(2+)-Mediated Switch of Epiplakin from a Diffuse to Keratin-Bound State Affects Keratin Dynamics |
title_short | A Ca(2+)-Mediated Switch of Epiplakin from a Diffuse to Keratin-Bound State Affects Keratin Dynamics |
title_sort | ca(2+)-mediated switch of epiplakin from a diffuse to keratin-bound state affects keratin dynamics |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563781/ https://www.ncbi.nlm.nih.gov/pubmed/36231039 http://dx.doi.org/10.3390/cells11193077 |
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