Ledreux Aurélie, Krys Sophie, Bernard Cécile
Unité Ecosystèmes et interactions toxiques, USM 0505/EA 4105 MNHN, Muséum National d'Histoire Naturelle, Case 39, 12 rue Buffon, F-75231 Paris Cedex 5, France.
Toxicon. 2009 Feb;53(2):300-8. doi: 10.1016/j.toxicon.2008.12.005. Epub 2008 Dec 11.
Palytoxin and related compounds are neurotoxic phycotoxins produced by benthic microalgae belonging to the genus Ostreopsis. For several years this family of phycotoxins has been posing a threat to human health since they can bioaccumulate in shellfish. With the aim of replacing current biological assays, such as the mouse or hemolytic assays, we investigated using the Neuro-2a neuroblastoma cell line to detect palytoxin and related compounds. Cell death induced by the effects of PlTX and analogues on Na+, K+-ATPase were measured using the 1-(4,5-dimethylthiazol-2-yl)-3,5-diphenylformazan (MTT) assay for mitochondrial reductase activity as a surrogate for cell number. The specificity of the Neuro-2a cell-based assay for palytoxin detection was confirmed by using ouabain, which also acts on Na+, K+-ATPase. Pre-treatment of the Neuro-2a cells with ouabain minimizes the effects of palytoxin. The specificity of the Neuro-2a assay was confirmed by the finding that cell death was not detected when Neuro-2a cells were exposed to other phycotoxins with unrelated cellular targets. When the Neuro-2a assay was used to detect palytoxin in mussel extracts spiked with levels of palytoxin around the proposed regulatory value of 250 microg palytoxin/kg shellfish, a good correlation was observed between the levels found and the expected values. We conclude by proposing an experimental design for functional assays using the Neuro-2a cell line for the specific detection of four neurotoxic phycotoxin families: saxitoxins, brevetoxins, ciguatoxins and palytoxins.
岩沙海葵毒素及相关化合物是由底栖微藻奥氏藻属产生的神经毒性藻毒素。多年来,这类藻毒素一直对人类健康构成威胁,因为它们可在贝类中生物累积。为了取代当前的生物检测方法,如小鼠或溶血检测,我们研究了使用Neuro-2a神经母细胞瘤细胞系来检测岩沙海葵毒素及相关化合物。使用1-(4,5-二甲基噻唑-2-基)-3,5-二苯基甲臜(MTT)法检测线粒体还原酶活性作为细胞数量的替代指标,以测量PlTX及其类似物对Na⁺、K⁺-ATP酶作用诱导的细胞死亡。通过使用同样作用于Na⁺、K⁺-ATP酶的哇巴因,证实了基于Neuro-2a细胞的岩沙海葵毒素检测方法的特异性。用哇巴因预处理Neuro-2a细胞可使岩沙海葵毒素的影响最小化。当Neuro-2a细胞暴露于具有不相关细胞靶点的其他藻毒素时未检测到细胞死亡,这一发现证实了Neuro-2a检测方法的特异性。当使用Neuro-2a检测方法检测添加了约250微克岩沙海葵毒素/千克贝类的建议监管值水平的贻贝提取物中的岩沙海葵毒素时,所发现的水平与预期值之间观察到良好的相关性。我们通过提出一种实验设计来得出结论,该实验设计使用Neuro-2a细胞系进行功能检测,以特异性检测四个神经毒性藻毒素家族:石房蛤毒素、短裸甲藻毒素、雪卡毒素和岩沙海葵毒素。