Antagonistic effect of picolinic acid and interferon-gamma on macrophage inflammatory protein-1alpha/beta production

Cell Immunol. 2002 Nov;220(1):70-80. doi: 10.1016/s0008-8749(03)00008-x.

Abstract

The L-tryptophan catabolite, picolinic acid (PA), is an activator of macrophage effector functions and an inducer of macrophage inflammatory protein-1alpha (MIP-1alpha) and -1beta (MIPs). We have investigated the regulation of PA-induced MIPs production in mouse macrophages. We demonstrated a dose- and time-dependent downregulation of MIPs mRNA by the Th1 cytokine, IFN-gamma, that was associated with inhibition of intracellular chemokine production and secretion. This effect was IFN-gamma-specific because MIPs induction was unaffected by the Th2 cytokines, IL-10 and IL-4, or the proinflammatory stimulus, LPS. Moreover, MIPs downregulation by IFN-gamma was dependent on both mRNA destabilization and gene transcription inhibition. These results demonstrate that MIP-1alpha/beta production by macrophages is a tightly regulated process resulting from the interaction between inhibitory stimuli derived from the immune system and stimulatory signals of non-immunologic origin. The antagonistic effect of PA and IFN-gamma on MIPs production may be important for the regulation of the inflammatory responses in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Transformed / drug effects
  • Chemokine CCL3
  • Chemokine CCL4
  • Depression, Chemical
  • Dose-Response Relationship, Radiation
  • Gene Expression Regulation / drug effects*
  • Half-Life
  • Interferon-gamma / pharmacology*
  • Interleukin-10 / pharmacology
  • Interleukin-4 / pharmacology
  • Macrophage Activation / drug effects*
  • Macrophage Activation / genetics
  • Macrophage Inflammatory Proteins / biosynthesis*
  • Macrophage Inflammatory Proteins / genetics
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Macrophages, Peritoneal / drug effects
  • Macrophages, Peritoneal / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Picolinic Acids / pharmacology*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Transcription, Genetic

Substances

  • Chemokine CCL3
  • Chemokine CCL4
  • Macrophage Inflammatory Proteins
  • Picolinic Acids
  • RNA, Messenger
  • Interleukin-10
  • Interleukin-4
  • Interferon-gamma
  • picolinic acid

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