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


ABSTRACT: 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.

SUBMITTER: Thomas DG 

PROVIDER: S-EPMC4539979 | biostudies-literature | 2015 Aug

REPOSITORIES: biostudies-literature

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

Thomas Dustin G DG   Yenepalli Aishwarya A   Denais Celine Marie CM   Rape Andrew A   Beach Jordan R JR   Wang Yu-Li YL   Schiemann William P WP   Baskaran Harihara H   Lammerding Jan J   Egelhoff Thomas T TT  

The Journal of cell biology 20150810 4


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 fo  ...[more]

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