Alteration of the parasite plasma membrane and the parasitophorous vacuole membrane during exo-erythrocytic development of malaria parasites

Protist. 2009 Feb;160(1):51-63. doi: 10.1016/j.protis.2008.08.002. Epub 2008 Nov 20.

Abstract

The rodent malaria parasite Plasmodium berghei develops in hepatocytes within 48-52h from a single sporozoite into up to 20,000 daughter parasites, so-called merozoites. The cellular and molecular details of this extensive proliferation are still largely unknown. Here we have used a transgenic, RFP-expressing P. berghei parasite line and molecular imaging techniques including intravital microscopy to decipher various aspects of parasite development within the hepatocyte. In late schizont stages, MSP1 is expressed and incorporated into the parasite plasma membrane that finally forms the membrane of developing merozoites by continuous invagination steps. We provide first evidence for activation of a verapamil-sensitive Ca(2+) channel in the plasma membrane of liver stage parasites before invagination occurs. During merozoite formation, the permeability of the parasitophorous vacuole membrane changes considerably before it finally becomes completely disrupted, releasing merozoites into the host cell cytoplasm.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium Channels / metabolism
  • Cell Line
  • Cell Membrane / metabolism*
  • Cell Membrane Permeability
  • Hepatocytes / parasitology
  • Humans
  • Liver / parasitology
  • Malaria / parasitology*
  • Merozoites / growth & development
  • Mice
  • Microscopy, Electron, Transmission
  • Microscopy, Fluorescence / methods
  • Plasmodium berghei / growth & development*
  • Rats
  • Sporozoites / growth & development
  • Vacuoles / metabolism*
  • Verapamil

Substances

  • Calcium Channels
  • Verapamil