Force-induced recruitment of cten along keratin network in epithelial cells

Proc Natl Acad Sci U S A. 2019 Oct 1;116(40):19799-19801. doi: 10.1073/pnas.1911865116. Epub 2019 Sep 16.

Abstract

The cytoskeleton provides structural integrity to cells and serves as a key component in mechanotransduction. Tensins are thought to provide a force-bearing linkage between integrins and the actin cytoskeleton; yet, direct evidence of tensin's role in mechanotransduction is lacking. We here report that local force application to epithelial cells using a micrometer-sized needle leads to rapid accumulation of cten (tensin 4), but not tensin 1, along a fibrous intracellular network. Surprisingly, cten-positive fibers are not actin fibers; instead, these fibers are keratin intermediate filaments. The dissociation of cten from tension-free keratin fibers depends on the duration of cell stretch, demonstrating that the external force favors maturation of cten-keratin network interactions over time and that keratin fibers retain remarkable structural memory of a cell's force-bearing state. These results establish the keratin network as an integral part of force-sensing elements recruiting distinct proteins like cten and suggest the existence of a mechanotransduction pathway via keratin network.

Keywords: cytoskeleton; keratin; mechanotransduction; simple epithelia; tensin.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cell Movement
  • Cytoskeleton / chemistry*
  • Dogs
  • Epithelial Cells / chemistry*
  • Humans
  • Image Processing, Computer-Assisted
  • Keratins / chemistry
  • Madin Darby Canine Kidney Cells
  • Mechanotransduction, Cellular*
  • Microfilament Proteins / chemistry
  • Stress, Mechanical*
  • Tensins / chemistry*

Substances

  • Microfilament Proteins
  • TNS1 protein, human
  • TNS4 protein, human
  • Tensins
  • Keratins