Two distinct modes of myosin assembly and dynamics during epithelial wound closure

J Cell Biol. 2007 Jan 1;176(1):27-33. doi: 10.1083/jcb.200609116.

Abstract

Actomyosin contraction powers the sealing of epithelial sheets during embryogenesis and wound closure; however, the mechanisms are poorly understood. After laser ablation wounding of Madin-Darby canine kidney cell monolayers, we observed distinct steps in wound closure from time-lapse images of myosin distribution during resealing. Immediately upon wounding, actin and myosin II regulatory light chain accumulated at two locations: (1) in a ring adjacent to the tight junction that circumscribed the wound and (2) in fibers at the base of the cell in membranes extending over the wound site. Rho-kinase activity was required for assembly of the myosin ring, and myosin II activity was required for contraction but not for basal membrane extension. As it contracted, the myosin ring moved toward the basal membrane with ZO-1 and Rho-kinase. Thus, we suggest that tight junctions serve as attachment points for the actomyosin ring during wound closure and that Rho-kinase is required for localization and activation of the contractile ring.

Publication types

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

MeSH terms

  • Actomyosin / metabolism
  • Animals
  • Cell Adhesion
  • Cell Polarity
  • Cell Shape
  • Chickens
  • Dogs
  • Epithelial Cells / cytology*
  • Epithelial Cells / enzymology
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Myosin Light Chains / chemistry*
  • Myosin Light Chains / metabolism*
  • Protein Serine-Threonine Kinases / metabolism
  • Protein Structure, Quaternary
  • Tight Junctions / metabolism
  • Wound Healing / physiology*
  • rho-Associated Kinases

Substances

  • Intracellular Signaling Peptides and Proteins
  • Myosin Light Chains
  • Actomyosin
  • Protein Serine-Threonine Kinases
  • rho-Associated Kinases