Pharmacological modulation of LPS-induced MIP-1 alpha production by peripheral blood mononuclear cells

Pharmacology. 1998 May;56(5):230-6. doi: 10.1159/000028202.

Abstract

In the present study, we investigated the effects of some anti-asthmatic drugs on the production of the CC chemokine, macrophage inflammatory protein-1 alpha (MIP-1 alpha), in response to lipopolysaccharide (LPS) by peripheral blood mononuclear cells (PBMC). MIP-1 alpha production was induced by LPS in a concentration-dependent fashion and reached the maximum at 10 micrograms/ml LPS (27.5 +/- 2.3 ng MIP-1 alpha/10(6) PBMC). At a submaximal concentration of LPS (1 microgram/ml), the release of MIP-1 alpha increased with time and reached the maximum 24 h after LPS stimulation. Actinomycin D and cycloheximide inhibited MIP-1 alpha production completely, but glucocorticoids did not completely inhibit MIP-1 alpha production, with a maximum inhibition of 70%. We examined the effect of beta-stimulants and phosphodiesterase inhibitors, which upregulate intracellular cyclic AMP levels, on MIP-1 alpha production. When PBMC were treated with beta-stimulants alone, beta-stimulants showed a slightly inhibitory effect on MIP-1 alpha production. However, the coadministration of roliplam significantly potentiated the inhibitory effect of beta-stimulants on MIP-1 alpha production. Moreover, db-cAMP suppressed MIP-1 alpha production dose-dependently. The above data indicate that the production of MIP-1 alpha is regulated by cyclic AMP and that cyclic AMP could provide a useful target for therapeutic treatment in asthmatic diseases and other diseases where MIP-1 alpha is involved in their etiology.

MeSH terms

  • Adrenergic beta-Agonists / pharmacology
  • Anti-Asthmatic Agents / pharmacology*
  • Bucladesine / pharmacology
  • Chemokine CCL4
  • Endotoxins
  • Escherichia coli*
  • Glucocorticoids / pharmacology
  • Humans
  • In Vitro Techniques
  • Lipopolysaccharides / pharmacology*
  • Macrophage Inflammatory Proteins / biosynthesis*
  • Monocytes / drug effects
  • Monocytes / metabolism*
  • Phosphodiesterase Inhibitors / pharmacology
  • Protein Synthesis Inhibitors / pharmacology

Substances

  • Adrenergic beta-Agonists
  • Anti-Asthmatic Agents
  • Chemokine CCL4
  • Endotoxins
  • Glucocorticoids
  • Lipopolysaccharides
  • Macrophage Inflammatory Proteins
  • Phosphodiesterase Inhibitors
  • Protein Synthesis Inhibitors
  • Bucladesine
  • endotoxin, Escherichia coli