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Published on: May 31, 2018
Ricin induces IL-8 secretion from human monocyte/macrophages by activating the p38 MAP kinase pathway
Tessa V Gonzalez1, Stephanie A Farrant, Nicholas J Mantis
1Department of Pediatrics, Harvard Medical School, and GI Cell Biology Laboratory, Children's Hospital Boston, Boston, MA 02115, USA.
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.
Insights
Ricin toxin triggers human immune cells to release IL-8, a key molecule in inflammation. This process involves the p38 MAPK pathway, suggesting potential therapeutic targets for ricin-induced inflammation.
Area of Science:
- Immunology
- Toxicology
- Cell Biology
Background:
- Polymorphonuclear cell (PMN) infiltration is characteristic of ricin-induced mucosal inflammation.
- The specific cellular mechanisms initiating this inflammatory response are not fully understood.
Purpose of the Study:
- To investigate the cellular response of human monocyte/macrophages to ricin exposure.
- To identify the signaling pathways involved in ricin-induced IL-8 secretion.
Main Methods:
- Human monocyte/macrophage cell line (28SC) was exposed to ricin.
- Interleukin-8 (IL-8) secretion levels were measured.
- The role of p38 mitogen-activated protein kinase (MAPK) was assessed using an inhibitor (SB203580).
Main Results:
- Ricin stimulated 28SC cells to secrete IL-8 in a dose- and time-dependent manner.
- IL-8 secretion was dependent on active ricin translocation and involved p38 MAPK activation.
- Inhibition of p38 MAPK suppressed ricin-induced IL-8 release.
Conclusions:
- Ricin induces IL-8 production in human monocyte/macrophages via p38 MAPK pathway activation.
- This finding suggests p38 MAPK inhibitors could be potential therapeutics for ricin intoxication-related mucosal inflammation.
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