Agents that elevate cAMP inhibit human neutrophil apoptosis

Biochem Biophys Res Commun. 1995 Dec 26;217(3):892-9. doi: 10.1006/bbrc.1995.2855.

Abstract

Neutrophil apoptosis, determined after 20 h in culture using standard criteria and shedding of cell surface CD16 (Fc gamma RIII), is dramatically inhibited, in a concentration-dependent manner, by the cAMP analogs, dibutyryl-cAMP and 8-Br-cAMP, and the adenylyl cyclase activator, forskolin. Furthermore, the stable receptor-directed PGD2 mimetic, ZK 118.182, and the PGE2 mimetic, 11-deoxy PGE1, similarly inhibited apoptosis. The DP-receptor antagonist BW A868C blocked the effect of ZK 118.182 and the protein kinase A inhibitor H-89 reversed the inhibition of apoptosis induced by dibutyryl-cAMP. These results clearly show that neutrophil apoptosis is markedly attenuated by cAMP elevating agents. This nucleotide second messenger may play a fundamental role in controlling neutrophil longevity and pharmacological regulation of cAMP levels or actions may influence neutrophil apoptosis in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alprostadil / analogs & derivatives
  • Alprostadil / pharmacology
  • Apoptosis / drug effects*
  • Cells, Cultured
  • Colforsin / pharmacology
  • Cyclic AMP / physiology*
  • Cyclic AMP-Dependent Protein Kinases / antagonists & inhibitors
  • Dinoprost / analogs & derivatives
  • Dinoprost / pharmacology
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Isoquinolines / pharmacology
  • Neutrophils / cytology*
  • Neutrophils / drug effects
  • Prostaglandins E, Synthetic / pharmacology
  • Receptors, IgG / metabolism
  • Sulfonamides*

Substances

  • Enzyme Inhibitors
  • Isoquinolines
  • Prostaglandins E, Synthetic
  • Receptors, IgG
  • Sulfonamides
  • ZK 118182
  • Colforsin
  • Dinoprost
  • Cyclic AMP
  • Cyclic AMP-Dependent Protein Kinases
  • Alprostadil
  • N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide
  • 11-deoxyprostaglandin E1