Interleukin-13 down-regulates the expression of neutrophil-derived macrophage inflammatory protein-1 alpha

Inflamm Res. 1998 Sep;47(9):361-8. doi: 10.1007/s000110050345.

Abstract

Objective and design: To determine whether interleukin-13 (IL-13) possesses anti-inflammatory properties with respect to polymorphonuclear neutrophils (PMNs). Effects of IL-13 on production of the chemokine, macrophage inflammatory protein-1 alpha (MIP-1alpha), by PMNs were analyzed.

Subjects: Human peripheral blood PMNs obtained from healthy volunteers.

Methods: PMNs were stimulated by lipopolysaccharide (LPS) and/or IL-13 for selected periods of time, and MIP-1alpha expression was assessed by ELISA and Northern blot analysis.

Results: IL-13 suppressed expression and production of PMN-derived MIP-1alpha mRNA and protein in a dose- and time-dependent manner. Inhibition of protein synthesis caused significant enhancement of MIP-1alpha mRNA expression. The inhibitory activity of IL-13 was abrogated, however, in the presence of cycloheximide, suggesting that IL-13's effect was via synthesis of de novo repressor protein(s).

Conclusions: PMN-derived chemokines are regulated by both proinflammatory and immunomodulatory cytokines. The coordinated production of these substances is likely to be important in the orchestration of inflammatory and immune responses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Northern
  • Cells, Cultured
  • Chemokine CCL3
  • Chemokine CCL4
  • Cycloheximide / pharmacology
  • DNA-Directed RNA Polymerases / antagonists & inhibitors
  • Dactinomycin / pharmacology
  • Down-Regulation
  • Enzyme Inhibitors / pharmacology
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • Interleukin-13 / pharmacology
  • Interleukin-13 / physiology*
  • Interleukin-8 / biosynthesis
  • Lipopolysaccharides / pharmacology
  • Macrophage Inflammatory Proteins / biosynthesis*
  • Neutrophil Activation
  • Neutrophils / drug effects
  • Neutrophils / metabolism*
  • Protein Synthesis Inhibitors / pharmacology
  • RNA, Messenger / biosynthesis
  • Recombinant Proteins / pharmacology

Substances

  • Chemokine CCL3
  • Chemokine CCL4
  • Enzyme Inhibitors
  • Interleukin-13
  • Interleukin-8
  • Lipopolysaccharides
  • Macrophage Inflammatory Proteins
  • Protein Synthesis Inhibitors
  • RNA, Messenger
  • Recombinant Proteins
  • Dactinomycin
  • Cycloheximide
  • DNA-Directed RNA Polymerases