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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...

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Autores principales: Stewart, Rachel M., Zubek, Amanda E., Rosowski, Kathryn A., Schreiner, Sarah M., Horsley, Valerie, King, Megan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2015
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.
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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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