Effect of tumor necrosis factor-alpha on intracellular Staphylococcus aureus in vascular endothelial cells

FEMS Immunol Med Microbiol. 2008 Mar;52(2):247-52. doi: 10.1111/j.1574-695X.2007.00365.x. Epub 2008 Jan 3.

Abstract

Although tumor necrosis factor-alpha (TNF-alpha) is an important host factor against intracellular bacteria, little is known about the effect of TNF-alpha on the persistence of intracellular Staphylococcus aureus in vascular endothelial cells. It was investigated whether recombinant human TNF-alpha influences the survival of intracellular S. aureus (ATCC 29213) in human umbilical vein endothelial cells (HUVEC) under a condition with an antistaphylococcal agent, and its mechanism. The HUVECs were incubated with TNF-alpha, oxacillin, or both in 24-well plates for up to 48 h following internalization of S. aureus (10(6) CFU well(-1)) into HUVECs for 1 h. TNF-alpha (1 ng mL(-1)) significantly reduced the number of intracellular S. aureus in HUVECs, and TNF-alpha plus oxacillin eliminated more intracellular S. aureus in HUVEC than oxacillin alone. The LDH viability assay and quantification of apoptosis using photometric enzyme-immunoassay showed that TNF-alpha preferentially induced cell death and apoptosis of HUVECs infected with S. aureus compared with noninfected HUVECs. These results indicate that TNF-alpha helps antistaphylococcal antibiotics to eliminate intracellular S. aureus in vascular endothelial cells, partly because TNF-alpha preferentially induces apoptosis of endothelial cells infected by S. aureus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Apoptosis
  • Cell Line
  • Colony Count, Microbial
  • Endothelial Cells / microbiology*
  • Humans
  • L-Lactate Dehydrogenase / metabolism
  • Microbial Viability
  • Oxacillin / pharmacology
  • Staphylococcus aureus / drug effects*
  • Tumor Necrosis Factor-alpha / immunology*

Substances

  • Anti-Bacterial Agents
  • Tumor Necrosis Factor-alpha
  • L-Lactate Dehydrogenase
  • Oxacillin