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Non-muscle myosin IIB is critical for nuclear translocation during 3D invasion

Non-muscle myosin II (NMII) is reported to play multiple roles during cell migration and invasion. However, the exact biophysical roles of different NMII isoforms during these processes remain poorly understood. We analyzed the contributions of NMIIA and NMIIB in three-dimensional (3D) migration and...

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Autores principales: Thomas, Dustin G., Yenepalli, Aishwarya, Denais, Celine Marie, Rape, Andrew, Beach, Jordan R., Wang, Yu-li, Schiemann, William P., Baskaran, Harihara, Lammerding, Jan, Egelhoff, Thomas T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539979/
https://www.ncbi.nlm.nih.gov/pubmed/26261182
http://dx.doi.org/10.1083/jcb.201502039
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author Thomas, Dustin G.
Yenepalli, Aishwarya
Denais, Celine Marie
Rape, Andrew
Beach, Jordan R.
Wang, Yu-li
Schiemann, William P.
Baskaran, Harihara
Lammerding, Jan
Egelhoff, Thomas T.
author_facet Thomas, Dustin G.
Yenepalli, Aishwarya
Denais, Celine Marie
Rape, Andrew
Beach, Jordan R.
Wang, Yu-li
Schiemann, William P.
Baskaran, Harihara
Lammerding, Jan
Egelhoff, Thomas T.
author_sort Thomas, Dustin G.
collection PubMed
description Non-muscle myosin II (NMII) is reported to play multiple roles during cell migration and invasion. However, the exact biophysical roles of different NMII isoforms during these processes remain poorly understood. We analyzed the contributions of NMIIA and NMIIB in three-dimensional (3D) migration and in generating the forces required for efficient invasion by mammary gland carcinoma cells. Using traction force microscopy and microfluidic invasion devices, we demonstrated that NMIIA is critical for generating force during active protrusion, and NMIIB plays a major role in applying force on the nucleus to facilitate nuclear translocation through tight spaces. We further demonstrate that the nuclear membrane protein nesprin-2 is a possible linker coupling NMIIB-based force generation to nuclear translocation. Together, these data reveal a central biophysical role for NMIIB in nuclear translocation during 3D invasive migration, a result with relevance not only to cancer metastasis but for 3D migration in other settings such as embryonic cell migration and wound healing.
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spelling pubmed-45399792016-02-17 Non-muscle myosin IIB is critical for nuclear translocation during 3D invasion Thomas, Dustin G. Yenepalli, Aishwarya Denais, Celine Marie Rape, Andrew Beach, Jordan R. Wang, Yu-li Schiemann, William P. Baskaran, Harihara Lammerding, Jan Egelhoff, Thomas T. J Cell Biol Research Articles Non-muscle myosin II (NMII) is reported to play multiple roles during cell migration and invasion. However, the exact biophysical roles of different NMII isoforms during these processes remain poorly understood. We analyzed the contributions of NMIIA and NMIIB in three-dimensional (3D) migration and in generating the forces required for efficient invasion by mammary gland carcinoma cells. Using traction force microscopy and microfluidic invasion devices, we demonstrated that NMIIA is critical for generating force during active protrusion, and NMIIB plays a major role in applying force on the nucleus to facilitate nuclear translocation through tight spaces. We further demonstrate that the nuclear membrane protein nesprin-2 is a possible linker coupling NMIIB-based force generation to nuclear translocation. Together, these data reveal a central biophysical role for NMIIB in nuclear translocation during 3D invasive migration, a result with relevance not only to cancer metastasis but for 3D migration in other settings such as embryonic cell migration and wound healing. The Rockefeller University Press 2015-08-17 /pmc/articles/PMC4539979/ /pubmed/26261182 http://dx.doi.org/10.1083/jcb.201502039 Text en 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
Thomas, Dustin G.
Yenepalli, Aishwarya
Denais, Celine Marie
Rape, Andrew
Beach, Jordan R.
Wang, Yu-li
Schiemann, William P.
Baskaran, Harihara
Lammerding, Jan
Egelhoff, Thomas T.
Non-muscle myosin IIB is critical for nuclear translocation during 3D invasion
title Non-muscle myosin IIB is critical for nuclear translocation during 3D invasion
title_full Non-muscle myosin IIB is critical for nuclear translocation during 3D invasion
title_fullStr Non-muscle myosin IIB is critical for nuclear translocation during 3D invasion
title_full_unstemmed Non-muscle myosin IIB is critical for nuclear translocation during 3D invasion
title_short Non-muscle myosin IIB is critical for nuclear translocation during 3D invasion
title_sort non-muscle myosin iib is critical for nuclear translocation during 3d invasion
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539979/
https://www.ncbi.nlm.nih.gov/pubmed/26261182
http://dx.doi.org/10.1083/jcb.201502039
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