Alternariol (AOH) is a low-molecular-weight mycotoxin produced by Alternaria species, frequently found in cereal grains, tomatoes, and processed foods. While its genotoxic and endocrine-disrupting effects are well established, emerging studies suggest a neurotoxic potential that remains poorly understood. Astrocytes-key regulators of neuronal support and calcium (Ca2+) balance in the central nervous system (CNS)-are an underexplored target of AOH toxicity. Here, we investigated the effects of AOH on Ca2+ signaling and viability in human astrocytes (Gibco Human Astrocyte, GHA cells). AOH exposure (25-125 μM) caused a concentration-dependent rise in cytosolic Ca2+ concentrations (Ca2+ᵢ) and induced significant cytotoxicity. These effects were reversed by the intracellular Ca2+ chelator BAPTA-AM, suggesting a Ca2+-dependent mechanism. Mechanistically, AOH mobilized Ca2+ from the endoplasmic reticulum (ER), as shown by thapsigargin blockade, and facilitated extracellular influx via store-operated calcium entry (SOCE), inhibited by 2-APB (a SOCE inhibitor) and GF109203X (a protein kinase C, PKC inhibitor). Notably, inhibition of phospholipase C (PLC) by U73122 completely abolished the Ca2+ rise, implicating the PLC-ER axis as a key upstream trigger. Together, our findings reveal a novel Ca2+-dependent mechanism by which AOH disrupts astrocyte homeostasis, providing new insights into its neurotoxic potential and highlighting Ca2+ signaling as a potential therapeutic target in glial toxicology.
Chen et al. (Thu,) studied this question.