Regulation of interleukin-6 production by prostaglandin E2 in fetal rat osteoblasts: role of protein kinase A signaling pathway

J Bone Miner Res. 1998 Jul;13(7):1092-100. doi: 10.1359/jbmr.1998.13.7.1092.

Abstract

Prostaglandin E2 (PGE2) is an abundant eicosanoid in bone that has been implicated in a number of pathological states associated with bone loss. Interleukin-6 (IL-6) is a cytokine that plays a critical role in bone remodeling and appears to act as a downstream effector of most bone-resorbing agents. In light of the evidence that PGE2 induces IL-6 in the bone environment, this study was designed to investigate whether PGE2 regulated IL-6 expression by osteoblasts. Here we demonstrate that PGE2 is a potent inducer of IL-6 production by fetal rat osteoblasts and synergizes with lipopolysaccharide to enhance IL-6. We show that PGE2 stimulates the activity of the IL-6 promoter in osteoblasts, suggesting that PGE2 controls IL-6 gene expression at least at the transcriptional level. Moreover, we show that PGE2-mediated IL-6 induction is prevented by the cAMP antagonist, Rp-cAMP, and the protein kinase A (PKA) inhibitors, KT5720 and H89. Thus, our data indicate that PGE2 involves the cAMP-PKA signaling pathway to regulate IL-6 gene expression in osteoblasts.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Carbazoles*
  • Cyclic AMP / analogs & derivatives
  • Cyclic AMP / pharmacology
  • Cyclic AMP-Dependent Protein Kinases / antagonists & inhibitors
  • Cyclic AMP-Dependent Protein Kinases / metabolism*
  • Dinoprostone / pharmacology*
  • Enzyme Inhibitors / pharmacology
  • Indoles / pharmacology
  • Interleukin-6 / biosynthesis*
  • Interleukin-6 / genetics
  • Isoquinolines / pharmacology
  • Osteoblasts / drug effects*
  • Osteoblasts / metabolism
  • Promoter Regions, Genetic
  • Pyrroles / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Sulfonamides*
  • Thionucleotides / pharmacology
  • Transcription, Genetic / drug effects

Substances

  • Carbazoles
  • Enzyme Inhibitors
  • Indoles
  • Interleukin-6
  • Isoquinolines
  • Pyrroles
  • Sulfonamides
  • Thionucleotides
  • adenosine-3',5'-cyclic phosphorothioate
  • KT 5720
  • Cyclic AMP
  • Cyclic AMP-Dependent Protein Kinases
  • Dinoprostone
  • N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide