Extracellular potassium deprivation reversibly dephosphorylates cofilin

Biochem Biophys Res Commun. 2006 Jul 14;345(4):1393-7. doi: 10.1016/j.bbrc.2006.05.028. Epub 2006 May 12.

Abstract

Cofilin is essential for actin filament remodeling in various cell types. We previously reported that ouabain leads to dephosphorylation of cofilin, resulting in cytoskeletal reorganization and cell volume change. We report here that the extracellular [K(+)](e) deprivation causes dephosphorylation of cofilin with disruption of cytoskeletal structures and cell shrinkage. These changes can be reversed by time-dependent restoration of [K(+)](e). Thus, these results suggest that the acute shift of [K(+)](e) triggers a reversible change of cofilin phosphorylation which may be an essential event in the regulation of cytoskeletal architecture and cell volume.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Depolymerizing Factors / metabolism*
  • Animals
  • Cell Size / drug effects
  • Cytoskeleton / drug effects
  • Cytoskeleton / metabolism
  • Dose-Response Relationship, Drug
  • Mice
  • NIH 3T3 Cells
  • Phosphorylation / drug effects
  • Potassium / pharmacology*
  • Time Factors

Substances

  • Actin Depolymerizing Factors
  • Potassium