Cell-substrate distance fluctuations of confluent cells enable fast and coherent collective migration

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Marcel Jipp - , University of Göttingen (Author)
  • Bente D. Wagner - , University of Göttingen (Author)
  • Lisa Egbringhoff - , University of Göttingen (Author)
  • Andreas Teichmann - , University of Göttingen (Author)
  • Angela Rübeling - , University of Göttingen (Author)
  • Paul Nieschwitz - , University of Göttingen (Author)
  • Alf Honigmann - , Chair of Biophysics (Author)
  • Alexey Chizhik - , University of Göttingen (Author)
  • Tabea A. Oswald - , University of Göttingen (Author)
  • Andreas Janshoff - , University of Göttingen (Author)

Abstract

Collective cell migration is an emergent phenomenon, with long-range cell-cell communication influenced by various factors, including transmission of forces, viscoelasticity of individual cells, substrate interactions, and mechanotransduction. We investigate how alterations in cell-substrate distance fluctuations, cell-substrate adhesion, and traction forces impact the average velocity and temporal-spatial correlation of confluent monolayers formed by either wild-type (WT) MDCKII cells or zonula occludens (ZO)-1/2-depleted MDCKII cells (double knockdown [dKD]) representing highly contractile cells. The data indicate that confluent dKD monolayers exhibit decreased average velocity compared to less contractile WT cells concomitant with increased substrate adhesion, reduced traction forces, a more compact shape, diminished cell-cell interactions, and reduced cell-substrate distance fluctuations. Depletion of basal actin and myosin further supports the notion that short-range cell-substrate interactions, particularly fluctuations driven by basal actomyosin, significantly influence the migration speed of the monolayer on a larger length scale.

Details

Original languageEnglish
Article number114553
JournalCell reports
Volume43
Issue number8
Publication statusPublished - 27 Aug 2024
Peer-reviewedYes

External IDs

PubMed 39150846
ORCID /0000-0003-0475-3790/work/190134724

Keywords

Keywords

  • atomic force microscopy, cell mechanics, collective cell migration, CP: Cell biology, jamming, tight junctions, traction force microscopy