Sink or swim: lipid rafts in parasite pathogenesis

Trends Parasitol. 2012 Oct;28(10):417-26. doi: 10.1016/j.pt.2012.07.002. Epub 2012 Aug 18.

Abstract

Lipid rafts, sterol- and sphingolipid-rich membrane microdomains, have been extensively studied in mammalian cells. Recently, lipid rafts have been shown to control virulence in a variety of parasites including Entamoeba histolytica, Giardia intestinalis, Leishmania spp., Plasmodium spp., Toxoplasma gondii, and Trypanosoma spp. Parasite rafts regulate adhesion to host and invasion, and parasite adhesion molecules often localize to rafts. Parasite rafts also control vesicle trafficking, motility, and cell signaling. Parasites disrupt host cell rafts; the dysregulation of host membrane function facilitates the establishment of infection and evasion of the host immune system. Discerning the mechanism by which lipid rafts regulate parasite pathogenesis is essential to our understanding of virulence. Such insight may guide the development of new drugs for disease management.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Animals
  • Cell Adhesion / physiology
  • Endocytosis
  • Eukaryota / immunology
  • Eukaryota / pathogenicity
  • Eukaryota / physiology*
  • Host-Parasite Interactions*
  • Humans
  • Immune System Phenomena
  • Membrane Microdomains / parasitology*
  • Protozoan Infections / parasitology*
  • Protozoan Proteins / metabolism
  • Signal Transduction

Substances

  • Protozoan Proteins