IL-1 beta inhibits ET-1 production by ATII cells in vitro: evidence for involvement of cyclooxygenase 2 pathway

Am J Physiol. 1997 Jul;273(1 Pt 1):L193-200. doi: 10.1152/ajplung.1997.273.1.L193.

Abstract

The aim of this study was to characterize the effect of alveolar macrophage (AM) secretory products on endothelin (ET)-1 production by rat alveolar type II (ATII) cells in primary culture. We quantified preproendothelin (ppET)-1 mRNA by Northern blot and ET-1 concentrations in cell supernatants by enzyme-linked immunosorbent assay. Conditioned medium (CM) from rat adherent AM decreased the ppET-1 mRNA levels in ATII cells and reduced ET-1 concentrations in cell culture supernatants. This effect was mediated by interleukin (IL)-1 beta as shown by pretreatment of CM with an anti-IL-1 beta neutralizing antiserum. IL-1 beta effect was dependent on protein synthesis, was partially prevented with indomethacin, and was totally prevented with dexamethasone. Specific inhibition of cyclooxygenase 2 activity completely reversed the effect of IL-1 beta. We conclude that rat AM inhibit ET-1 production by rat ATII cells in vitro through IL-1 beta secretion. The IL-1 beta-mediated inhibition is dependent on the cyclooxygenase 2 pathway. Downregulation of ET-1 production by activated AM could limit the intra-alveolar burden of this profibrogenic peptide and thus could prevent fibrosis development.

MeSH terms

  • Animals
  • Bronchoalveolar Lavage Fluid
  • Cells, Cultured
  • Culture Media, Conditioned
  • Cyclooxygenase 2
  • Dactinomycin / pharmacology
  • Endothelin-1 / antagonists & inhibitors
  • Endothelin-1 / biosynthesis*
  • Endothelins / biosynthesis*
  • Humans
  • Interleukin-1 / pharmacology*
  • Interleukin-6 / pharmacology
  • Isoenzymes / metabolism*
  • Macrophages, Alveolar / physiology*
  • Male
  • Membrane Proteins
  • Prostaglandin-Endoperoxide Synthases / metabolism*
  • Protein Precursors / biosynthesis*
  • Pulmonary Alveoli / cytology
  • Pulmonary Alveoli / drug effects
  • Pulmonary Alveoli / metabolism*
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins / pharmacology
  • Transcription, Genetic / drug effects
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Culture Media, Conditioned
  • Endothelin-1
  • Endothelins
  • Interleukin-1
  • Interleukin-6
  • Isoenzymes
  • Membrane Proteins
  • Protein Precursors
  • RNA, Messenger
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • Dactinomycin
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases