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Nuclear–cytoskeletal linkages facilitate cross talk between the nucleus and intercellular adhesions
The linker of nucleoskeleton and cytoskeleton (LINC) complex allows cells to actively control nuclear position by coupling the nucleus to the cytoplasmic cytoskeleton. Nuclear position responds to the formation of intercellular adhesions through coordination with the cytoskeleton, but it is not know...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4427780/ https://www.ncbi.nlm.nih.gov/pubmed/25963820 http://dx.doi.org/10.1083/jcb.201502024 |
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author | Stewart, Rachel M. Zubek, Amanda E. Rosowski, Kathryn A. Schreiner, Sarah M. Horsley, Valerie King, Megan C. |
author_facet | Stewart, Rachel M. Zubek, Amanda E. Rosowski, Kathryn A. Schreiner, Sarah M. Horsley, Valerie King, Megan C. |
author_sort | Stewart, Rachel M. |
collection | PubMed |
description | The linker of nucleoskeleton and cytoskeleton (LINC) complex allows cells to actively control nuclear position by coupling the nucleus to the cytoplasmic cytoskeleton. Nuclear position responds to the formation of intercellular adhesions through coordination with the cytoskeleton, but it is not known whether this response impacts adhesion function. In this paper, we demonstrate that the LINC complex component SUN2 contributes to the mechanical integrity of intercellular adhesions between mammalian epidermal keratinocytes. Mice deficient for Sun2 exhibited irregular hair follicle intercellular adhesions, defective follicle structure, and alopecia. Primary mouse keratinocytes lacking Sun2 displayed aberrant nuclear position in response to adhesion formation, altered desmosome distribution, and mechanically defective adhesions. This dysfunction appeared rooted in a failure of Sun2-null cells to reorganize their microtubule network to support coordinated intercellular adhesion. Together, these results suggest that cross talk between the nucleus, cytoskeleton, and intercellular adhesions is important for epidermal tissue integrity. |
format | Online Article Text |
id | pubmed-4427780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44277802015-11-11 Nuclear–cytoskeletal linkages facilitate cross talk between the nucleus and intercellular adhesions Stewart, Rachel M. Zubek, Amanda E. Rosowski, Kathryn A. Schreiner, Sarah M. Horsley, Valerie King, Megan C. J Cell Biol Research Articles The linker of nucleoskeleton and cytoskeleton (LINC) complex allows cells to actively control nuclear position by coupling the nucleus to the cytoplasmic cytoskeleton. Nuclear position responds to the formation of intercellular adhesions through coordination with the cytoskeleton, but it is not known whether this response impacts adhesion function. In this paper, we demonstrate that the LINC complex component SUN2 contributes to the mechanical integrity of intercellular adhesions between mammalian epidermal keratinocytes. Mice deficient for Sun2 exhibited irregular hair follicle intercellular adhesions, defective follicle structure, and alopecia. Primary mouse keratinocytes lacking Sun2 displayed aberrant nuclear position in response to adhesion formation, altered desmosome distribution, and mechanically defective adhesions. This dysfunction appeared rooted in a failure of Sun2-null cells to reorganize their microtubule network to support coordinated intercellular adhesion. Together, these results suggest that cross talk between the nucleus, cytoskeleton, and intercellular adhesions is important for epidermal tissue integrity. The Rockefeller University Press 2015-05-11 /pmc/articles/PMC4427780/ /pubmed/25963820 http://dx.doi.org/10.1083/jcb.201502024 Text en © 2015 Stewart et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Stewart, Rachel M. Zubek, Amanda E. Rosowski, Kathryn A. Schreiner, Sarah M. Horsley, Valerie King, Megan C. Nuclear–cytoskeletal linkages facilitate cross talk between the nucleus and intercellular adhesions |
title | Nuclear–cytoskeletal linkages facilitate cross talk between the nucleus and intercellular adhesions |
title_full | Nuclear–cytoskeletal linkages facilitate cross talk between the nucleus and intercellular adhesions |
title_fullStr | Nuclear–cytoskeletal linkages facilitate cross talk between the nucleus and intercellular adhesions |
title_full_unstemmed | Nuclear–cytoskeletal linkages facilitate cross talk between the nucleus and intercellular adhesions |
title_short | Nuclear–cytoskeletal linkages facilitate cross talk between the nucleus and intercellular adhesions |
title_sort | nuclear–cytoskeletal linkages facilitate cross talk between the nucleus and intercellular adhesions |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4427780/ https://www.ncbi.nlm.nih.gov/pubmed/25963820 http://dx.doi.org/10.1083/jcb.201502024 |
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