Plasmodium berghei-infection induces volume-regulated anion channel-like activity in human hepatoma cells

Cell Microbiol. 2009 Oct;11(10):1492-501. doi: 10.1111/j.1462-5822.2009.01342.x. Epub 2009 Jun 3.

Abstract

Parasite infection can lead to alterations in the permeability of host plasma membranes. Presented here is the first demonstration that this phenomenon occurs in Plasmodium-infected liver cells. Using the whole-cell patch-clamp technique, volume-regulated anion channel (VRAC) activity was characterized in Huh-7 cells (a human hepatoma cell line) before and after infection with Plasmodium berghei. Consistent with the presence of VRACs, hypotonic bath solution induced large ion currents in Huh-7 cells that rectified outwardly, reversed close to the equilibrium potential for Cl(-) and were inhibited by tamoxifen, clomiphene, mefloquine and 5-nitro-2, 3-(phenylpropylamino)-benzoic acid (NPPB), with IC(50) values of 4 +/- 1, 4 +/- 2, 2 +/- 1 and 52 +/- 12 microM respectively. In isotonic conditions, initial current recordings measured in uninfected and immature (24 h post invasion) parasite-infected Huh-7 cells were similar (with conductances of 14 +/- 3 versus 19 +/- 5 pS/pF). However, in mature (48-72 h post invasion) parasite-infected Huh-7 cells there was a sevenfold increase in currents (with a conductance of 98 +/- 16 pS/pF). The elevated currents observed in the latter are consistent with VRAC-like activity and the possible reasons for their activation are discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anions / metabolism*
  • Cell Membrane Permeability / physiology*
  • Cell Size
  • Chlorine / metabolism
  • Clomiphene / pharmacology
  • Enzyme Inhibitors / pharmacology
  • Hepatocytes / parasitology*
  • Humans
  • Ion Channels / drug effects
  • Ion Channels / metabolism*
  • Mefloquine / pharmacology
  • Nitrobenzoates / pharmacology
  • Plasmodium berghei / growth & development*
  • Tamoxifen / pharmacology

Substances

  • Anions
  • Enzyme Inhibitors
  • Ion Channels
  • Nitrobenzoates
  • Tamoxifen
  • Clomiphene
  • 5-nitro-2-(3-phenylpropylamino)benzoic acid
  • Chlorine
  • Mefloquine