Tumor necrosis factor stimulates prostaglandin production and cyclic AMP levels in rat cultured mesangial cells

FEBS Lett. 1988 Oct 24;239(1):50-4. doi: 10.1016/0014-5793(88)80543-x.

Abstract

Human recombinant tumor necrosis factor-alpha (TNF) was found to stimulate the production of prostaglandins (PG) by cultured rat mesangial cells. This effect was demonstrable from 6 h, was dose dependent and affected the synthesis of PGE2, PGF2 alpha, and 6-keto-PGF1 alpha. It required both RNA and protein synthesis but was not associated with a modification of cell proliferation. TNF also stimulated adenosine 3'-5' cyclic monophosphate (cAMP) levels in the mesangial cell culture medium. Indomethacin suppressed the effect of TNF on PGs but only reduced that on cAMP, indicating that PG production partly mediates the increase in cAMP. These findings demonstrate that mesangial cells can be a target for TNF and that the mechanism of TNF action includes stimulation of both PG production and cAMP levels.

MeSH terms

  • 6-Ketoprostaglandin F1 alpha / biosynthesis
  • Animals
  • Cells, Cultured
  • Cyclic AMP / metabolism*
  • Cycloheximide / pharmacology
  • Dactinomycin / pharmacology
  • Dinoprost / biosynthesis
  • Dinoprostone / biosynthesis
  • Glomerular Mesangium / drug effects
  • Glomerular Mesangium / metabolism*
  • Indomethacin / pharmacology
  • Kidney Cortex / drug effects
  • Kidney Cortex / metabolism
  • Kinetics
  • Prostaglandins / biosynthesis*
  • Rats
  • Rats, Inbred Strains
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Prostaglandins
  • Tumor Necrosis Factor-alpha
  • Dactinomycin
  • 6-Ketoprostaglandin F1 alpha
  • Cycloheximide
  • Dinoprost
  • Cyclic AMP
  • Dinoprostone
  • Indomethacin