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Cytotoxicity of yessotoxin and okadaic acid in mouse T lymphocyte cell line EL-4
Alicia Martín-López1, Juan J Gallardo-Rodríguez, Asterio Sánchez-Mirón
1Department of Chemical Engineering, University of Almería, Crta. de Sacramento s/n, La Cañada, 04120 Almería, Spain. alicia@ual.es
Abstract:
Yessotoxin (YTX) and okadaic acid (OA), algal toxins accumulated in edible shellfish, were previously shown to induce a specific and reversible T Cell Receptor (TCR) down-regulation in T lymphocyte EL-4 cells, in a time and concentration-dependent manner, via protein kinase C (PKC) and serine/threonine protein phosphatase 2A (PP2A) activities. In this study we have evaluated the development of other signs of toxicity induced by low concentrations of YTX or OA for 3 days of treatment. Concentrations of YTX as low as 1 nM decreased a 35% the concentration of viable cells after 48 h exposure to the toxin, while concentrations as little as 5 nM YTX or OA were sufficient to induce membrane blebbing. The concentration of YTX that produced after 24 h of incubation a 50% reduction in maximum cell viability (EC50₂₄) was approximately 46 nM, whereas with OA over 75% of the cells were still viable after exposure to 100 nM OA. According to our results, the cytoskeleton of EL-4 cells seems to be a cell component particularly sensitive to YTX and OA with disruption of F-actin cytoskeleton in these cells treated with concentrations of YTX or OA as low as 5 nM at 48 h incubation. Toxicity by YTX or OA involved typical hallmarks of apoptosis and an increase of reactive oxygen species (ROS) production. The cytotoxic effects of YTX and OA reported here, and the previously demonstrated potential of these toxins to regulate the activity of EL-4 cells through the regulation of TCR expression, rise reasonable concern about possible risks for human health associated to the chronic exposure to low amounts of YTX or OA itself or enhanced by the presence of other shellfish toxins specially by a population potentially at risk such as immunocompromised patients.
Insights
Yessotoxin and okadaic acid, shellfish toxins, cause cell death, membrane damage, and cytoskeleton disruption in T cells. These toxins, even at low concentrations, induce apoptosis and increase reactive oxygen species, raising health concerns.
Area of Science:
- Marine Biology
- Immunotoxicology
- Cell Biology
Background:
- Yessotoxin (YTX) and okadaic acid (OA) are marine algal toxins found in shellfish.
- Previous studies showed YTX and OA down-regulate T Cell Receptor (TCR) expression via protein kinase C (PKC) and protein phosphatase 2A (PP2A).
Purpose of the Study:
- To investigate other toxic effects of low-concentration YTX and OA exposure on T lymphocyte EL-4 cells.
- To assess cytotoxicity, membrane integrity, cytoskeleton disruption, apoptosis, and reactive oxygen species (ROS) production.
Main Methods:
- EL-4 cells were treated with varying concentrations of YTX and OA for up to 3 days.
- Cell viability, membrane blebbing, F-actin cytoskeleton integrity, and ROS production were analyzed.
- Apoptosis hallmarks were evaluated.
Main Results:
- Low YTX concentrations (1 nM) reduced viable cell count by 35% within 48 hours.
- YTX and OA (5 nM) induced membrane blebbing and F-actin cytoskeleton disruption within 48 hours.
- YTX exhibited an EC50 of approximately 46 nM for cell viability reduction after 24 hours, while OA was less potent.
Conclusions:
- YTX and OA exhibit significant cytotoxicity, impacting cell viability, membrane integrity, and cytoskeleton structure.
- Apoptosis and increased ROS production are key mechanisms of YTX and OA toxicity.
- Chronic exposure to these toxins, especially in immunocompromised individuals, poses potential health risks.
