Vascular endothelial cells cultured from patients with cerebral or uncomplicated malaria exhibit differential reactivity to TNF

Cell Microbiol. 2011 Feb;13(2):198-209. doi: 10.1111/j.1462-5822.2010.01528.x. Epub 2010 Oct 7.

Abstract

Plasmodium falciparum malaria is a major cause of morbidity and mortality in African children, and factors that determine the development of uncomplicated (UM) versus cerebral malaria (CM) are not fully understood. We studied the ex vivo responsiveness of microvascular endothelial cells to pro-inflammatory stimulation and compared the findings between CM and UM patients. In patients with fatal disease we compared the properties of vascular endothelial cells cultured from brain tissue to those cultured from subcutaneous tissue, and found them to be very similar. We then isolated, purified and cultured primary endothelial cells from aspirated subcutaneous tissue of patients with CM (EC(CM) ) or UM (EC(UM) ) and confirmed the identity of the cells before analysis. Upon TNF stimulation in vitro, EC(CM) displayed a significantly higher capacity to upregulate ICAM-1, VCAM-1 and CD61 and to produce IL-6 and MCP-1 but not RANTES compared with EC(UM) . The shedding of endothelial microparticles, a recently described parameter of severity in CM, and the cellular level of activated caspase-3 were both significantly greater in EC(CM) than in EC(UM) . These data suggest that inter-individual differences in the endothelial inflammatory response to TNF may be an additional factor influencing the clinical course of malaria.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain / immunology
  • Cell-Derived Microparticles / metabolism
  • Cells, Cultured
  • Chemokine CCL2 / biosynthesis
  • Chemokine CCL5 / biosynthesis
  • Endothelial Cells / immunology*
  • Humans
  • Integrin beta3 / biosynthesis
  • Intercellular Adhesion Molecule-1 / biosynthesis
  • Interleukin-6 / biosynthesis
  • Malaria, Falciparum / immunology*
  • Malaria, Falciparum / pathology
  • Plasmodium falciparum / immunology*
  • Plasmodium falciparum / pathogenicity
  • Tumor Necrosis Factor-alpha / immunology*
  • Vascular Cell Adhesion Molecule-1 / biosynthesis

Substances

  • CCL2 protein, human
  • CCL5 protein, human
  • Chemokine CCL2
  • Chemokine CCL5
  • IL6 protein, human
  • ITGB3 protein, human
  • Integrin beta3
  • Interleukin-6
  • TNF protein, human
  • Tumor Necrosis Factor-alpha
  • Vascular Cell Adhesion Molecule-1
  • Intercellular Adhesion Molecule-1