Human herpesvirus 8 acute infection of endothelial cells induces monocyte chemoattractant protein 1-dependent capillary-like structure formation: role of the IKK/NF-kappaB pathway

Blood. 2007 Apr 1;109(7):2718-26. doi: 10.1182/blood-2006-03-012500.

Abstract

Human herpesvirus 8 (HHV-8) is considered the causative agent of Kaposi sarcoma, a highly vascularized neoplasm characterized by spindle-shaped cells of endothelial origin and inflammatory cell infiltration. The cell transforming ability of HHV-8 has been associated with the activation of NF-kappaB, a nuclear factor playing a pivotal role in promoting inflammation and cell proliferation; however, little is known about NF-kappaB activation during acute HHV-8 infection. In the present study, we used a recently established in vitro model of HHV-8 acute productive infection in endothelial cells to investigate the effect of HHV-8 on NF-kappaB activity and function. HHV-8 rapidly and potently induced NF-kappaB activity in endothelial cells via stimulation of the IkappaB kinase (IKK). Following IKK activation, HHV-8 selectively triggered the production of high levels of monocyte chemoattractant protein 1 (MCP-1), whereas it did not affect the expression of other NF-kappaB-dependent proinflammatory proteins, including TNF-alpha, IL-8, and RANTES. Deletion of NF-kappaB-binding sites in the MCP-1 enhancer resulted in significant inhibition of HHV-8-induced transcription. Furthermore, MCP-1 production was accompanied by virus-induced capillary-like structure formation at early stages of infection. The results suggest that HHV-8-induced MCP-1 may play an important role in promoting inflammation and pathogenic angiogenesis typical of HHV-8-associated lesions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Capillaries / pathology
  • Cells, Cultured
  • Chemokine CCL2 / genetics
  • Chemokine CCL2 / physiology*
  • Endothelial Cells / pathology
  • Endothelial Cells / physiology*
  • Gene Expression
  • Herpesviridae Infections / genetics
  • Herpesviridae Infections / pathology
  • Herpesviridae Infections / virology
  • Herpesvirus 8, Human / genetics
  • Herpesvirus 8, Human / pathogenicity*
  • Humans
  • I-kappa B Kinase / physiology*
  • NF-kappa B / physiology*
  • Neovascularization, Pathologic
  • Sarcoma, Kaposi / blood supply
  • Sarcoma, Kaposi / etiology
  • Sarcoma, Kaposi / genetics
  • Sarcoma, Kaposi / virology

Substances

  • CCL2 protein, human
  • Chemokine CCL2
  • NF-kappa B
  • I-kappa B Kinase