Human T-cell leukemia virus type I tax transactivates the interleukin-6 gene in human rheumatoid synovial cells

J Rheumatol. 1995 Nov;22(11):2049-54.

Abstract

Objective: To determine the effect of the human T cell leukemia virus type I (HTLV-I) tax gene on interleukin-6 (IL-6) production and gene transcription in synovial cells, we established the synovial cell line, E-11, from a patient with rheumatoid arthritis.

Methods: E-11 cells were transfected with tax expression vector using the calcium phosphate coprecipitation method. IL-6 production and gene expression were investigated by ELISA and Northern blot analysis, respectively. To clarify how tax induces IL-6 gene expression, we used deletion analysis and chloramphenicol acetyltransferase (CAT) assay, and electrophoretic mobility shift assay (EMSA).

Results: Transfection of the tax gene induced markedly high levels of IL-6 mRNA. Furthermore, the tax gene strongly transactivated IL-6 gene promoter activity assayed by CAT assay. By using deletion and site specific mutations, we have identified a nuclear factor (NF)-kappa B sequence (positions -73 to -63) which is essential for tax transaction. EMSA demonstrated the induction of specific binding of nuclear extracts to the NF-kappa B sequence by HTLV-I tax.

Conclusion: The HTLV-1 tax gene may transactivate IL-6 gene in the synovial cells through NF-kappa B and may contribute in the pathophysiology of HTLV-I associated arthritis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arthritis, Rheumatoid / genetics
  • Arthritis, Rheumatoid / pathology
  • Arthritis, Rheumatoid / virology*
  • Base Sequence
  • Cell Nucleus / chemistry
  • Genes, pX / physiology*
  • Human T-lymphotropic virus 1 / genetics*
  • Humans
  • Interleukin-6 / genetics*
  • Molecular Probes / genetics
  • Molecular Sequence Data
  • NF-kappa B / metabolism
  • Promoter Regions, Genetic
  • Synovial Membrane / pathology
  • Synovial Membrane / virology*
  • Tissue Extracts / metabolism
  • Transcription, Genetic
  • Transcriptional Activation*

Substances

  • Interleukin-6
  • Molecular Probes
  • NF-kappa B
  • Tissue Extracts