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A WAVE2–Arp2/3 actin nucleator apparatus supports junctional tension at the epithelial zonula adherens

The epithelial zonula adherens (ZA) is a specialized adhesive junction where actin dynamics and myosin-driven contractility coincide. The junctional cytoskeleton is enriched in myosin II, which generates contractile force to support junctional tension. It is also enriched in dynamic actin filaments,...

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Autores principales: Verma, Suzie, Han, Siew Ping, Michael, Magdalene, Gomez, Guillermo A., Yang, Zhe, Teasdale, Rohan D., Ratheesh, Aparna, Kovacs, Eva M., Ali, Radiya G., Yap, Alpha S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510021/
https://www.ncbi.nlm.nih.gov/pubmed/23051739
http://dx.doi.org/10.1091/mbc.E12-08-0574
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author Verma, Suzie
Han, Siew Ping
Michael, Magdalene
Gomez, Guillermo A.
Yang, Zhe
Teasdale, Rohan D.
Ratheesh, Aparna
Kovacs, Eva M.
Ali, Radiya G.
Yap, Alpha S.
author_facet Verma, Suzie
Han, Siew Ping
Michael, Magdalene
Gomez, Guillermo A.
Yang, Zhe
Teasdale, Rohan D.
Ratheesh, Aparna
Kovacs, Eva M.
Ali, Radiya G.
Yap, Alpha S.
author_sort Verma, Suzie
collection PubMed
description The epithelial zonula adherens (ZA) is a specialized adhesive junction where actin dynamics and myosin-driven contractility coincide. The junctional cytoskeleton is enriched in myosin II, which generates contractile force to support junctional tension. It is also enriched in dynamic actin filaments, which are replenished by ongoing actin assembly. In this study we sought to pursue the relationship between actin assembly and junctional contractility. We demonstrate that WAVE2–Arp2/3 is a major nucleator of actin assembly at the ZA and likely acts in response to junctional Rac signaling. Furthermore, WAVE2–Arp2/3 is necessary for junctional integrity and contractile tension at the ZA. Maneuvers that disrupt the function of either WAVE2 or Arp2/3 reduced junctional tension and compromised the ability of cells to buffer side-to-side forces acting on the ZA. WAVE2–Arp2/3 disruption depleted junctions of both myosin IIA and IIB, suggesting that dynamic actin assembly may support junctional tension by facilitating the local recruitment of myosin.
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spelling pubmed-35100212013-02-16 A WAVE2–Arp2/3 actin nucleator apparatus supports junctional tension at the epithelial zonula adherens Verma, Suzie Han, Siew Ping Michael, Magdalene Gomez, Guillermo A. Yang, Zhe Teasdale, Rohan D. Ratheesh, Aparna Kovacs, Eva M. Ali, Radiya G. Yap, Alpha S. Mol Biol Cell Articles The epithelial zonula adherens (ZA) is a specialized adhesive junction where actin dynamics and myosin-driven contractility coincide. The junctional cytoskeleton is enriched in myosin II, which generates contractile force to support junctional tension. It is also enriched in dynamic actin filaments, which are replenished by ongoing actin assembly. In this study we sought to pursue the relationship between actin assembly and junctional contractility. We demonstrate that WAVE2–Arp2/3 is a major nucleator of actin assembly at the ZA and likely acts in response to junctional Rac signaling. Furthermore, WAVE2–Arp2/3 is necessary for junctional integrity and contractile tension at the ZA. Maneuvers that disrupt the function of either WAVE2 or Arp2/3 reduced junctional tension and compromised the ability of cells to buffer side-to-side forces acting on the ZA. WAVE2–Arp2/3 disruption depleted junctions of both myosin IIA and IIB, suggesting that dynamic actin assembly may support junctional tension by facilitating the local recruitment of myosin. The American Society for Cell Biology 2012-12-01 /pmc/articles/PMC3510021/ /pubmed/23051739 http://dx.doi.org/10.1091/mbc.E12-08-0574 Text en © 2012 Verma et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology.
spellingShingle Articles
Verma, Suzie
Han, Siew Ping
Michael, Magdalene
Gomez, Guillermo A.
Yang, Zhe
Teasdale, Rohan D.
Ratheesh, Aparna
Kovacs, Eva M.
Ali, Radiya G.
Yap, Alpha S.
A WAVE2–Arp2/3 actin nucleator apparatus supports junctional tension at the epithelial zonula adherens
title A WAVE2–Arp2/3 actin nucleator apparatus supports junctional tension at the epithelial zonula adherens
title_full A WAVE2–Arp2/3 actin nucleator apparatus supports junctional tension at the epithelial zonula adherens
title_fullStr A WAVE2–Arp2/3 actin nucleator apparatus supports junctional tension at the epithelial zonula adherens
title_full_unstemmed A WAVE2–Arp2/3 actin nucleator apparatus supports junctional tension at the epithelial zonula adherens
title_short A WAVE2–Arp2/3 actin nucleator apparatus supports junctional tension at the epithelial zonula adherens
title_sort wave2–arp2/3 actin nucleator apparatus supports junctional tension at the epithelial zonula adherens
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510021/
https://www.ncbi.nlm.nih.gov/pubmed/23051739
http://dx.doi.org/10.1091/mbc.E12-08-0574
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