Dynamics and segregation of cell-matrix adhesions in cultured fibroblasts

Nat Cell Biol. 2000 Apr;2(4):191-6. doi: 10.1038/35008607.

Abstract

Here we use time-lapse microscopy to analyse cell-matrix adhesions in cells expressing one of two different cytoskeletal proteins, paxillin or tensin, tagged with green fluorescent protein (GFP). Use of GFP-paxillin to analyse focal contacts and GFP-tensin to study fibrillar adhesions reveals that both types of major adhesion are highly dynamic. Small focal contacts often translocate, by extending centripetally and contracting peripherally, at a mean rate of 19 micrometers per hour. Fibrillar adhesions arise from the medial ends of stationary focal contacts, contain alpha5beta1 integrin and tensin but not other focal-contact components, and associate with fibronectin fibrils. Fibrillar adhesions translocate centripetally at a mean rate of 18 micrometers per hour in an actomyosin-dependent manner. We propose a dynamic model for the regulation of cell-matrix adhesions and for transitions between focal contacts and fibrillar adhesions, with the ability of the matrix to deform functioning as a mechanical switch.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Actomyosin / metabolism
  • Bridged Bicyclo Compounds, Heterocyclic / pharmacology
  • Cell Adhesion / physiology*
  • Cells, Cultured
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism*
  • Cytoskeleton / drug effects
  • Cytoskeleton / physiology*
  • Extracellular Matrix / physiology*
  • Fibroblasts / cytology
  • Genes, Reporter
  • Green Fluorescent Proteins
  • Humans
  • Indicators and Reagents / metabolism
  • Luminescent Proteins / genetics
  • Microfilament Proteins / genetics
  • Microfilament Proteins / metabolism*
  • Paxillin
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism*
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Tensins
  • Thiazoles / pharmacology
  • Thiazolidines
  • Transfection

Substances

  • Actins
  • Bridged Bicyclo Compounds, Heterocyclic
  • Cytoskeletal Proteins
  • Indicators and Reagents
  • Luminescent Proteins
  • Microfilament Proteins
  • PXN protein, human
  • Paxillin
  • Phosphoproteins
  • Recombinant Proteins
  • Tensins
  • Thiazoles
  • Thiazolidines
  • Green Fluorescent Proteins
  • Actomyosin
  • latrunculin A