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Updated: Jul 18, 2026

A Simple Fluorescence-based Reporter Assay to Identify Cellular Components Required for Ricin Toxin A Chain (RTA) Trafficking in Yeast
Published on: December 15, 2017
Down-regulation of gene transcripts associated with ricin tolerance in human RPMI 2650 cells
L J Wilkinson1, M L Duffield, R W Titball
1Biomedical Sciences Department, Dstl Porton Down, Salisbury, Wiltshire SP4 0JQ, UK.
Abstract:
The present study sought to determine if novel therapeutic approaches against ricin intoxication could be identified from human respiratory tract cells selected for increased resistance to this toxin. Initial studies indicated that the RPMI 2650 line was an appropriate model, owing to its sensitivity to ricin. Tolerant cultures were developed by exposing cells to a graded series of ricin concentrations from 6 to 192 pM. This resulted in the generation of cultures whose LC(50) values were increased by up to 4-fold following exposure to up to 96 pM ricin and by up to 6-fold following exposure to up to 192 pM ricin, compared to control cultures. DNA microarrays were employed to determine the gene transcript expression profile of cultures with increased resistance to ricin to investigate which gene products mediate ricin resistance. Transcripts (10) were identified that were greater than 2-fold down-regulated in the cells tolerant to 96 pM ricin, whereas 48 transcripts were seen to be down-regulated in cultures tolerant to 192 pM ricin. Gene transcripts (5) were up-regulated 2-fold or more in the 192 pM tolerant cultures in comparison to unexposed cells. The results indicate that ricin tolerance is the product of complex changes in gene expression profiles, most of which were found to involve down-regulation of transcript expression. It may be possible to modulate the gene expression profiles associated with ricin tolerance for potential therapeutic purposes using drugs and antisense technologies.
Insights
Researchers developed ricin-tolerant human respiratory cells to find new therapies for ricin intoxication. Gene expression analysis revealed complex changes, mostly down-regulation, suggesting potential therapeutic targets for ricin resistance.
Area of Science:
- Toxicology
- Cell Biology
- Molecular Biology
Background:
- Ricin is a highly toxic protein produced by castor beans.
- Developing effective countermeasures against ricin intoxication is crucial for public health and biodefense.
- Understanding cellular mechanisms of ricin resistance can inform therapeutic strategies.
Purpose of the Study:
- To identify novel therapeutic targets for ricin intoxication.
- To investigate gene expression profiles in human respiratory cells selected for ricin resistance.
- To explore the potential for modulating gene expression for therapeutic benefit.
Main Methods:
- Development of ricin-tolerant human respiratory tract cell cultures (RPMI 2650).
- Exposure of cells to a graded series of ricin concentrations (6–192 pM).
- DNA microarray analysis to determine gene transcript expression profiles in tolerant cells.
Main Results:
- Ricin-tolerant cell cultures exhibited up to 6-fold increased LC(50) values compared to controls.
- Significant alterations in gene expression were observed, with most transcripts down-regulated.
- 10 transcripts were >2-fold down-regulated in cells tolerant to 96 pM ricin; 48 in cells tolerant to 192 pM ricin.
- 5 transcripts were ≥2-fold up-regulated in cells tolerant to 192 pM ricin.
Conclusions:
- Ricin tolerance in human respiratory cells results from complex gene expression changes, predominantly down-regulation.
- These findings suggest that modulating specific gene expression profiles could offer therapeutic avenues against ricin toxicity.
- Further research into drugs and antisense technologies targeting these profiles may yield effective treatments.
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