Autocrine role for interleukin-8 in Bartonella henselae-induced angiogenesis

Infect Immun. 2006 Sep;74(9):5185-90. doi: 10.1128/IAI.00622-06.

Abstract

The gram-negative bacterium Bartonella henselae is capable of causing angiogenic lesions as a result of infection. Previously, it has been shown that B. henselae infection can result in production of the chemokine interleukin-8 (IL-8). In this study, we demonstrated that monocytes, endothelial cells, and hepatocytes produce IL-8 in response to B. henselae infection. We also investigated the role of IL-8 in B. henselae-induced endothelial cell proliferation and capillary tube formation. Both in vitro angiogenesis assays were IL-8 dependent. B. henselae-mediated inhibition of apoptosis, as indicated by gene expression of Bax and Bcl-2, was also shown to be IL-8 dependent in endothelial cells. Furthermore, infection of endothelial cells with B. henselae stimulated upregulation of the IL-8 chemokine receptor CXCR2. Infection of human endothelial cells by B. henselae resulting in IL-8 production likely plays a central role in the ability of this organism to cause angiogenesis during infection.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Angiomatosis, Bacillary / genetics
  • Angiomatosis, Bacillary / immunology*
  • Angiomatosis, Bacillary / pathology
  • Apoptosis / genetics
  • Autocrine Communication
  • Bartonella henselae*
  • Capillaries / growth & development
  • Cell Proliferation
  • Cells, Cultured
  • Endothelium, Vascular / immunology
  • Endothelium, Vascular / microbiology
  • Endothelium, Vascular / pathology
  • Gene Expression
  • Hepatocytes / immunology
  • Humans
  • Immunoglobulin G / pharmacology
  • Interleukin-8 / antagonists & inhibitors
  • Interleukin-8 / genetics
  • Interleukin-8 / physiology*
  • Monocytes / immunology
  • Neovascularization, Pathologic / genetics
  • Neovascularization, Pathologic / immunology*
  • Neovascularization, Pathologic / pathology
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Receptors, Interleukin-8B / genetics
  • Receptors, Interleukin-8B / metabolism*
  • Up-Regulation
  • bcl-2-Associated X Protein / genetics

Substances

  • Immunoglobulin G
  • Interleukin-8
  • Proto-Oncogene Proteins c-bcl-2
  • Receptors, Interleukin-8B
  • bcl-2-Associated X Protein