Nov 5, 2019

Vimentin protects cells against nuclear rupture and DNA damage during migration

The Journal of Cell Biology
Alison Elise PattesonPaul A Janmey

Abstract

Mammalian cells frequently migrate through tight spaces during normal embryogenesis, wound healing, diapedesis, or in pathological situations such as metastasis. Nuclear size and shape are important factors in regulating the mechanical properties of cells during their migration through such tight spaces. At the onset of migratory behavior, cells often initiate the expression of vimentin, an intermediate filament protein that polymerizes into networks extending from a juxtanuclear cage to the cell periphery. However, the role of vimentin intermediate filaments (VIFs) in regulating nuclear shape and mechanics remains unknown. Here, we use wild-type and vimentin-null mouse embryonic fibroblasts to show that VIFs regulate nuclear shape and perinuclear stiffness, cell motility in 3D, and the ability of cells to resist large deformations. These changes increase nuclear rupture and activation of DNA damage repair mechanisms, which are rescued by exogenous reexpression of vimentin. Our findings show that VIFs provide mechanical support to protect the nucleus and genome during migration.

Mentioned in this Paper

Rupture
Size
Genome
DNA Repair
Three-dimensional
Cell Motility
Regulation of Intermediate Filament Depolymerization
Cell Nucleus
Embryonic Development
Anatomical Space Structure

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