Tzima Eleni, Serifi Iliana, Tsikari Ioanna, Alzualde Ainhoa, Leonardos Ioannis, Papamarcaki Thomais
Laboratory of Biological Chemistry, Medical School, University of Ioannina, 45110 Ioannina, Greece.
Division of Biomedical Research, Foundation for Research and Technology-Hellas, Institute of Molecular Biology and Biotechnology, 45110 Ιοannina, Greece.
Int J Mol Sci. 2017 Feb 9;18(2):365. doi: 10.3390/ijms18020365.
Microcystins are cyclic heptapeptides that constitute a diverse group of toxins produced by cyanobacteria. One of the most toxic variants of this family is microcystin-LR (MCLR) which is a potent inhibitor of protein phosphatase 2A (PP2A) and induces cytoskeleton alterations. In this study, zebrafish larvae exposed to 500 μg/L of MCLR for four days exhibited a 40% reduction of PP2A activity compared to the controls, indicating early effects of the toxin. Gene expression profiling of the MCLR-exposed larvae using microarray analysis revealed that keratin 96 () was the most downregulated gene, consistent with the well-documented effects of MCLR on cytoskeleton structure. In addition, our analysis revealed upregulation in all genes encoding for the enzymes of the retinal visual cycle, including (retinal pigment epithelium-specific protein 65a), which is critical for the larval vision. Quantitative real-time PCR (qPCR) analysis confirmed the microarray data, showing that was significantly upregulated at 50 μg/L and 500 μg/L MCLR in a dose-dependent manner. Consistent with the microarray data, MCLR-treated larvae displayed behavioral alterations such as weakening response to the sudden darkness and hypoactivity in the dark. Our work reveals new molecular targets for MCLR and provides further insights into the molecular mechanisms of MCLR toxicity during early development.
微囊藻毒素是一类环状七肽,由蓝藻产生,包含多种毒素。该家族中毒性最强的变体之一是微囊藻毒素-LR(MCLR),它是蛋白磷酸酶2A(PP2A)的强效抑制剂,可诱导细胞骨架改变。在本研究中,暴露于500μg/L MCLR四天的斑马鱼幼体与对照组相比,PP2A活性降低了40%,表明该毒素具有早期效应。使用微阵列分析对暴露于MCLR的幼体进行基因表达谱分析,结果显示角蛋白96()是下调最明显的基因,这与MCLR对细胞骨架结构的广泛记录效应一致。此外,我们的分析显示,视网膜视觉循环中所有编码酶的基因均上调,包括对幼体视觉至关重要的(视网膜色素上皮特异性蛋白65a)。定量实时PCR(qPCR)分析证实了微阵列数据,表明在50μg/L和500μg/L MCLR处理下,以剂量依赖方式显著上调。与微阵列数据一致,经MCLR处理的幼体表现出行为改变,如对突然黑暗的反应减弱和在黑暗中活动减少。我们的工作揭示了MCLR的新分子靶点,并为早期发育过程中MCLR毒性的分子机制提供了进一步的见解。