Abstract
The intracellular parasite Toxoplasma gondii can penetrate any warm-blooded animal cell. Conserved molecular assemblies of host cell plasma membranes should be involved in the parasite-host cell recognition. Lipid rafts are well-conserved membrane microdomains that contain high concentrations of cholesterol, sphingolipids, glycosylphosphatidylinositol, GPI-anchored proteins, and dually acylated proteins such as members of the Src family of tyrosine kinases. Disturbing lipid rafts of mouse peritoneal macrophages and epithelial cells of the lineage LLC-MK2 with methyl-beta cyclodextrin (MβCD) and filipin, which interfere with cholesterol or lidocaine, significantly inhibited internalization of T. gondii in both cell types, although adhesion remained unaffected in macrophages and decreased only in LLC-MK2 cells. Scanning and transmission electron microscopy confirmed these observations. Results are discussed in terms of the original role of macrophages as professional phagocytes versus the LLC-MK2 cell lineage originated from kidney epithelial cells. © 2014 Karla Dias Cruz et al.
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CITATION STYLE
Cruz, K. D., Cruz, T. A., Veras De Moraes, G., Paredes-Santos, T. C., Attias, M., & De Souza, W. (2014). Disruption of lipid rafts interferes with the interaction of toxoplasma gondii with macrophages and epithelial cells. BioMed Research International, 2014. https://doi.org/10.1155/2014/687835
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