Connexin hemichannel composition determines the FGF-1-induced membrane permeability and free [Ca2+]i responses

Mol Biol Cell. 2008 Aug;19(8):3501-13. doi: 10.1091/mbc.e07-12-1240. Epub 2008 May 21.

Abstract

Cell surface hemichannels (HCs) composed of different connexin (Cx) types are present in diverse cells and their possible role on FGF-1-induced cellular responses remains unknown. Here, we show that FGF-1 transiently (4-14 h, maximal at 7 h) increases the membrane permeability through HCs in HeLa cells expressing Cx43 or Cx45 under physiological extracellular Ca(2+)/Mg(2+) concentrations. The effect does not occur in HeLa cells expressing HCs constituted of Cx26 or Cx43 with its C-terminus truncated at aa 257, or in parental nontransfected HeLa cells. The increase in membrane permeability is associated with a rise in HC levels at the cell surface and a proportional increase in HC unitary events. The response requires an early intracellular free Ca(2+) concentration increase, activation of a p38 MAP kinase-dependent pathway, and a regulatory site of Cx subunit C-terminus. The FGF-1-induced rise in membrane permeability is also associated with a late increase in intracellular free Ca(2+) concentration, suggesting that responsive HCs allow Ca(2+) influx. The cell density of Cx26 and Cx43 HeLa transfectants cultured in serum-free medium was differentially affected by FGF-1. Thus, the FGF-1-induced cell permeabilization and derived consequences depend on the Cx composition of HCs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium / metabolism*
  • Cell Membrane / metabolism
  • Connexin 26
  • Connexin 43 / metabolism
  • Connexins / metabolism*
  • Electrophysiology
  • Enzyme Activation
  • Fibroblast Growth Factor 1 / metabolism*
  • HeLa Cells
  • Humans
  • Microscopy, Fluorescence
  • Models, Biological
  • Permeability*
  • Protein Structure, Tertiary
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Connexin 43
  • Connexins
  • GJB2 protein, human
  • Fibroblast Growth Factor 1
  • Connexin 26
  • p38 Mitogen-Activated Protein Kinases
  • Calcium