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

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.