Interleukin-6 production in "normal" and HTLV-1 tax-expressing brain-specific endothelial cells

Eur J Immunol. 1993 Aug;23(8):1987-91. doi: 10.1002/eji.1830230839.

Abstract

Abnormal cytokine production can contribute in many instances to the development of pathology. Our study focuses on the regulation of interleukin (IL)-6 production in vitro in brain-specific endothelial cells (BEC) under physiological conditions and in a model of human T leukemia virus-1 (HTLV-1) infection. IL-6 production was strongly up-regulated in a dose-dependent mode upon exposure to recombinant IL-1 beta, although nearly not detectable in unstimulated BEC. This induction of IL-6 production could be achieved by reagents known to increase intracellular levels of cAMP, such as forskolin, prostaglandin E or pentoxifylline. Furthermore, transcription and production of IL-6 was inducible by addition of dibutyryl cAMP, but not by addition of calcium ionophores or diacylglycerol. To assess a potential role of HTLV-1-infected BEC in the pathogenesis of tropical spastic paraparesis (TSP), the HTLV-1 tax gene was expressed in BEC. Tax gene-expressing BEC produced constitutively very high amounts of IL-6, which were not longer hyperinducible by IL-1 beta or cAMP derivatives. Our results indicate that HTLV-1 tax induces hyperproduction of IL-6 in brain-specific endothelial cells directly by an intracellular mechanism which subsequently renders IL-6 production independent of exogenous stimuli or activators of (cAMP-dependent) second messenger levels. On the basis of these findings we suggest that tax-mediated hyperactivation of IL-6 production in BEC contributes to elevated IL-6 levels found in serum and cerebrospinal fluid of patients with TSP and might have a significance in the immune pathogenesis of the disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / metabolism*
  • Bucladesine / pharmacology
  • Cells, Cultured
  • Endothelium, Vascular / metabolism*
  • Genes, pX*
  • HTLV-I Infections / metabolism*
  • Interleukin-6 / biosynthesis*
  • Interleukin-6 / genetics
  • Mice
  • Mice, Inbred BALB C
  • RNA, Messenger / analysis
  • RNA, Messenger / genetics
  • Transfection

Substances

  • Interleukin-6
  • RNA, Messenger
  • Bucladesine