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Nesprin-3, a novel outer nuclear membrane protein, associates with the cytoskeletal linker protein plectin

Despite their importance in cell biology, the mechanisms that maintain the nucleus in its proper position in the cell are not well understood. This is primarily the result of an incomplete knowledge of the proteins in the outer nuclear membrane (ONM) that are able to associate with the different cyt...

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Autores principales: Wilhelmsen, Kevin, Litjens, Sandy H.M., Kuikman, Ingrid, Tshimbalanga, Ntambua, Janssen, Hans, van den Bout, Iman, Raymond, Karine, Sonnenberg, Arnoud
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2171291/
https://www.ncbi.nlm.nih.gov/pubmed/16330710
http://dx.doi.org/10.1083/jcb.200506083
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author Wilhelmsen, Kevin
Litjens, Sandy H.M.
Kuikman, Ingrid
Tshimbalanga, Ntambua
Janssen, Hans
van den Bout, Iman
Raymond, Karine
Sonnenberg, Arnoud
author_facet Wilhelmsen, Kevin
Litjens, Sandy H.M.
Kuikman, Ingrid
Tshimbalanga, Ntambua
Janssen, Hans
van den Bout, Iman
Raymond, Karine
Sonnenberg, Arnoud
author_sort Wilhelmsen, Kevin
collection PubMed
description Despite their importance in cell biology, the mechanisms that maintain the nucleus in its proper position in the cell are not well understood. This is primarily the result of an incomplete knowledge of the proteins in the outer nuclear membrane (ONM) that are able to associate with the different cytoskeletal systems. Two related ONM proteins, nuclear envelope spectrin repeat (nesprin)–1 and –2, are known to make direct connections with the actin cytoskeleton through their NH(2)-terminal actin-binding domain (ABD). We have now isolated a third member of the nesprin family that lacks an ABD and instead binds to the plakin family member plectin, which can associate with the intermediate filament (IF) system. Overexpression of nesprin-3 results in a dramatic recruitment of plectin to the nuclear perimeter, which is where these two molecules are colocalized with both keratin-6 and -14. Importantly, plectin binds to the integrin α6β4 at the cell surface and to nesprin-3 at the ONM in keratinocytes, suggesting that there is a continuous connection between the nucleus and the extracellular matrix through the IF cytoskeleton.
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spelling pubmed-21712912008-03-05 Nesprin-3, a novel outer nuclear membrane protein, associates with the cytoskeletal linker protein plectin Wilhelmsen, Kevin Litjens, Sandy H.M. Kuikman, Ingrid Tshimbalanga, Ntambua Janssen, Hans van den Bout, Iman Raymond, Karine Sonnenberg, Arnoud J Cell Biol Research Articles Despite their importance in cell biology, the mechanisms that maintain the nucleus in its proper position in the cell are not well understood. This is primarily the result of an incomplete knowledge of the proteins in the outer nuclear membrane (ONM) that are able to associate with the different cytoskeletal systems. Two related ONM proteins, nuclear envelope spectrin repeat (nesprin)–1 and –2, are known to make direct connections with the actin cytoskeleton through their NH(2)-terminal actin-binding domain (ABD). We have now isolated a third member of the nesprin family that lacks an ABD and instead binds to the plakin family member plectin, which can associate with the intermediate filament (IF) system. Overexpression of nesprin-3 results in a dramatic recruitment of plectin to the nuclear perimeter, which is where these two molecules are colocalized with both keratin-6 and -14. Importantly, plectin binds to the integrin α6β4 at the cell surface and to nesprin-3 at the ONM in keratinocytes, suggesting that there is a continuous connection between the nucleus and the extracellular matrix through the IF cytoskeleton. The Rockefeller University Press 2005-12-05 /pmc/articles/PMC2171291/ /pubmed/16330710 http://dx.doi.org/10.1083/jcb.200506083 Text en Copyright © 2005, The Rockefeller University Press 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 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Wilhelmsen, Kevin
Litjens, Sandy H.M.
Kuikman, Ingrid
Tshimbalanga, Ntambua
Janssen, Hans
van den Bout, Iman
Raymond, Karine
Sonnenberg, Arnoud
Nesprin-3, a novel outer nuclear membrane protein, associates with the cytoskeletal linker protein plectin
title Nesprin-3, a novel outer nuclear membrane protein, associates with the cytoskeletal linker protein plectin
title_full Nesprin-3, a novel outer nuclear membrane protein, associates with the cytoskeletal linker protein plectin
title_fullStr Nesprin-3, a novel outer nuclear membrane protein, associates with the cytoskeletal linker protein plectin
title_full_unstemmed Nesprin-3, a novel outer nuclear membrane protein, associates with the cytoskeletal linker protein plectin
title_short Nesprin-3, a novel outer nuclear membrane protein, associates with the cytoskeletal linker protein plectin
title_sort nesprin-3, a novel outer nuclear membrane protein, associates with the cytoskeletal linker protein plectin
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2171291/
https://www.ncbi.nlm.nih.gov/pubmed/16330710
http://dx.doi.org/10.1083/jcb.200506083
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