Human herpesvirus 8-derived viral IL-6 induces PTX3 expression in Kaposi's sarcoma cells

AIDS. 2002 May 24;16(8):F9-18. doi: 10.1097/00002030-200205240-00001.

Abstract

Objective: To analyse if human herpesvirus 8 (HHV8)-derived viral interleukin-6 (vIL-6) has the capacity to activate Kaposi's sarcoma (KS) cells to elicit a local acute-phase response.

Design: Proinflammatory activation of KS cells was compared using vIL-6, human IL-6, as well as the complex of human IL-6 with the soluble IL-6 receptor, and expression of the novel acute-phase protein pentraxin-3 (PTX3) was analysed.

Methods: We established primary KS cell cultures from patients with AIDS-associated and classical KS and expressed recombinant HHV8-derived vIL-6 in COS-7 cells. Expression of PTX3 by vIL-6-stimulated KS cell cultures was analysed by quantitative real-time reverse transcriptase-polymerase chain reaction. Mitogenic effects of vIL-6 on the KS cells of distinct aetiology were compared by [3H]thymidine incorporation.

Results: We show that vIL-6 induced a marked and sustained expression of the novel acute-phase protein PTX3 in human primary KS cell cultures. vIL-6 directly activated KS cells, which uniquely expressed gp130, the signal-transducing subunit of the IL-6 receptor, but were negative for the IL-6-binding unit (IL-6R). In contrast, human IL-6 did not stimulate KS cells in the absence of the full IL-6R. Expression of PTX3 messenger RNA increased by more than 25-fold in vIL-6-stimulated KS cells after 24 h. Particularly after extended incubation with the virokine, vIL-6 mediated a pronounced mitogenic effect on KS cells.

Conclusion: The induction of an extrahepatic acute-phase response by vIL-6-activated KS cells may contribute to local tissue damage and the attraction of inflammatory cells, and add to a more aggressive phenotype.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute-Phase Proteins / biosynthesis*
  • Acute-Phase Reaction
  • Animals
  • Antigens, CD / metabolism
  • C-Reactive Protein / biosynthesis*
  • COS Cells
  • Cell Division
  • Cells, Cultured
  • Cytokine Receptor gp130
  • Herpesvirus 8, Human / physiology*
  • Humans
  • Interleukin-6 / physiology*
  • Kinetics
  • Membrane Glycoproteins / metabolism
  • Receptors, Interleukin-6 / biosynthesis
  • Recombinant Proteins
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sarcoma, Kaposi / metabolism*
  • Serum Amyloid P-Component / biosynthesis*
  • Tumor Cells, Cultured
  • Viral Proteins / physiology*

Substances

  • Acute-Phase Proteins
  • Antigens, CD
  • IL6ST protein, human
  • Interleukin-6
  • Membrane Glycoproteins
  • Receptors, Interleukin-6
  • Recombinant Proteins
  • Serum Amyloid P-Component
  • Viral Proteins
  • Cytokine Receptor gp130
  • PTX3 protein
  • C-Reactive Protein