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Generation of compartmentalized pressure by a nuclear piston governs cell motility in a 3D matrix
Journal article   Open access   Peer reviewed

Generation of compartmentalized pressure by a nuclear piston governs cell motility in a 3D matrix

Ryan J Petrie, Hyun Koo and Kenneth M Yamada
Science (American Association for the Advancement of Science), v 345(6200), pp 1062-1065
29 Aug 2014
PMID: 25170155
url
https://europepmc.org/articles/pmc5248932View
Accepted (AM)Open Access (License Unspecified) Open

Abstract

Actomyosin - physiology Cell Movement - physiology Cell Nucleus - physiology Cells, Cultured Cytoplasm - physiology Extracellular Matrix - physiology Extracellular Matrix - ultrastructure Fibroblasts - physiology Humans Hydrostatic Pressure Microfilament Proteins Pseudopodia - physiology Vimentin - metabolism
Cells use actomyosin contractility to move through three-dimensional (3D) extracellular matrices. Contractility affects the type of protrusions cells use to migrate in 3D, but the mechanisms are unclear. In this work, we found that contractility generated high-pressure lobopodial protrusions in human cells migrating in a 3D matrix. In these cells, the nucleus physically divided the cytoplasm into forward and rear compartments. Actomyosin contractility with the nucleoskeleton-intermediate filament linker protein nesprin-3 pulled the nucleus forward and pressurized the front of the cell. Reducing expression of nesprin-3 decreased and equalized the intracellular pressure. Thus, the nucleus can act as a piston that physically compartmentalizes the cytoplasm and increases the hydrostatic pressure between the nucleus and the leading edge of the cell to drive lamellipodia-independent 3D cell migration.

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Collaboration types
Domestic collaboration
Web of Science research areas
Cell Biology
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