Ilimaquinone inhibits gap-junctional communication prior to Golgi fragmentation and block in protein transport

Exp Cell Res. 2003 Jul 1;287(1):130-42. doi: 10.1016/s0014-4827(03)00124-1.

Abstract

Brefeldin A and ilimaquinone are compounds known to affect Golgi structure and function. In particular, the transport of proteins is blocked either at the level of exit from endoplasmic reticulum (brefeldin) or at cis-Golgi (ilimaquinone). Brefeldin caused a slow decrease in gap-junctional communication and a slow loss of all phosphorylated forms of connexin43 in hamster and rat fibroblasts, while ilimaquinone caused an abrupt decrease in gap-junctional communication and rapid loss of only the slowest migrating phosphorylated connexin43 band (P2). Ilimaquinone caused these effects prior to any significant Golgi fragmentation, especially in hamster fibroblasts. Concurrently, ilimaquinone minimally affected protein secretion, while brefeldin caused an instantaneous decrease. These results show that ilimaquinone inhibits gap-junctional communication in connexin43-expressing cells by a mechanism not dependent on Golgi fragmentation or block in protein transport.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoantigens
  • Brefeldin A / pharmacology
  • Cell Communication / drug effects*
  • Cell Communication / physiology
  • Cells, Cultured
  • Coatomer Protein / drug effects
  • Coatomer Protein / metabolism
  • Connexin 43 / drug effects
  • Connexin 43 / metabolism
  • Cricetinae
  • Eukaryotic Cells / drug effects*
  • Eukaryotic Cells / metabolism
  • Eukaryotic Cells / ultrastructure
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Fibroblasts / ultrastructure
  • Gap Junctions / drug effects*
  • Gap Junctions / metabolism
  • Golgi Apparatus / drug effects*
  • Golgi Apparatus / pathology
  • Golgi Apparatus / ultrastructure
  • Immunohistochemistry
  • Membrane Proteins / drug effects
  • Membrane Proteins / metabolism
  • Microscopy, Electron
  • Protein Synthesis Inhibitors / pharmacology
  • Protein Transport / drug effects*
  • Protein Transport / physiology
  • Quinones / pharmacology*
  • Rats
  • Rats, Wistar
  • Sesquiterpenes / pharmacology*

Substances

  • Autoantigens
  • Coatomer Protein
  • Connexin 43
  • Golgin subfamily A member 2
  • Membrane Proteins
  • Protein Synthesis Inhibitors
  • Quinones
  • Sesquiterpenes
  • Brefeldin A
  • ilimaquinone