Ricin induces IL-8 secretion from human monocyte/macrophages by activating the p38 MAP kinase pathway

Mol Immunol. 2006 Apr;43(11):1920-3. doi: 10.1016/j.molimm.2005.11.002. Epub 2006 Jan 24.

Abstract

Polymorphonuclear cell (PMN) infiltration is a hallmark of ricin-induced mucosal inflammation, yet the cellular processes involved in initiating this reaction remain undefined. In this study we report that ricin stimulates the human monocyte/macrophages cell line 28SC to secrete IL-8, a potent PMN chemoattractant. IL-8 release in response to ricin was both dose- and time-dependent. 28SC cells did not secrete IL-8 when exposed to formaldehyde-inactivated holotoxin or ricin B subunit. Furthermore, IL-8 induction could be blocked by brefeldin A, which inhibits ricin translocation into the cytosol. As predicted from the literature, we observed elevated levels of p38 mitogen activated protein kinase (MAPK), a post-transcriptional regulator of IL-8, in 28SC cells as early as 3h after ricin exposure. Treatment of 28SC cells with the pyridylimidizole analogue SB203580, a known inhibitor of p38 MAPK, suppressed ricin-mediated IL-8 release. We conclude that ricin stimulates human monocyte/macrophages to produce IL-8 by activation of the p38 MAPK pathway, raising the possibility that p38 MAPK inhibitors may potentially serve as therapeutic agents to suppress mucosal inflammation associated with ricin intoxication.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Brefeldin A / pharmacology
  • Cycloheximide / pharmacology
  • Enzyme Activation / drug effects
  • Glycosides / pharmacology
  • Humans
  • Interleukin-8 / antagonists & inhibitors
  • Interleukin-8 / metabolism*
  • Macrophages / drug effects*
  • Macrophages / enzymology*
  • Macrophages / immunology
  • Macrophages / metabolism
  • Monocytes / drug effects*
  • Monocytes / enzymology*
  • Monocytes / immunology
  • Monocytes / metabolism
  • Ricin / pharmacology*
  • Triterpenes / pharmacology
  • p38 Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • p38 Mitogen-Activated Protein Kinases / metabolism*

Substances

  • Glycosides
  • Interleukin-8
  • Triterpenes
  • Brefeldin A
  • stichoposide
  • Ricin
  • Cycloheximide
  • p38 Mitogen-Activated Protein Kinases