Sandström von Tobel Jenny, Zoia Debora, Althaus Jorane, Antinori Paola, Mermoud Julien, Pak Hui Song, Scherl Alexander, Monnet-Tschudi Florianne
Swiss Centre for Applied Human Toxicology (SCAHT) , Switzerland; Department of Physiology, University of Lausanne, CH-1005 Lausanne, Switzerland.
Department of Physiology, University of Lausanne, CH-1005 Lausanne, Switzerland.
Toxicol Lett. 2014 Oct 15;230(2):188-97. doi: 10.1016/j.toxlet.2014.02.001. Epub 2014 Feb 9.
Xenobiotic exposure is a risk factor in the etiology of neurodegenerative disease. It was recently hypothesized that restricted exposure during brain development could predispose for a neurodegenerative disease later in life. As neuroinflammation contributes to progressive neurodegeneration, it is suspected that neurodevelopmental xenobiotic exposure could elicit a neuroinflammatory process, which over time may assume a detrimental character. We investigated the neurotoxic effects of paraquat (PQ) in three-dimensional whole rat brain cell cultures, exposed during an early differentiation stage, comparing immediate effects-directly post exposure-with long-term effects, 20 days after interrupted PQ-administration. Adverse effects and neuroinflammatory responses were assessed by measuring changes in gene- and protein-expression as well as by determining cell morphology changes. Differentiating neural cultures were highly susceptible to PQ and showed neuronal damage and strong astrogliosis. After the 20-day washout period, neurons partially recovered, whereas astrogliosis persisted, and was accompanied by microglial activation of a neurodegenerative phenotype. Our data shows that immediate and long-term effects of subchronic PQ-exposure differ. Also, PQ-exposure during this window of extensive neuronal differentiation led to a delayed microglial activation, of a character that could promote further pro-inflammatory signals that enable prolonged inflammation, thereby fueling further neurodegeneration.
外源性物质暴露是神经退行性疾病病因中的一个风险因素。最近有假说认为,大脑发育期间的有限暴露可能使人在晚年易患神经退行性疾病。由于神经炎症会导致进行性神经退行性变,因此怀疑神经发育过程中的外源性物质暴露可能引发神经炎症过程,随着时间的推移,这一过程可能会产生有害影响。我们研究了百草枯(PQ)在三维全大鼠脑细胞培养物中的神经毒性作用,这些培养物在早期分化阶段暴露,比较了暴露后立即产生的直接影响与PQ给药中断20天后的长期影响。通过测量基因和蛋白质表达的变化以及确定细胞形态变化来评估不良反应和神经炎症反应。正在分化的神经培养物对PQ高度敏感,表现出神经元损伤和强烈的星形胶质细胞增生。在20天的洗脱期后,神经元部分恢复,而星形胶质细胞增生持续存在,并伴有具有神经退行性表型的小胶质细胞激活。我们的数据表明,亚慢性PQ暴露的即时影响和长期影响有所不同。此外,在这个广泛神经元分化的窗口期暴露于PQ会导致小胶质细胞延迟激活,其特征可能会促进进一步的促炎信号,从而使炎症持续延长,进而加剧神经退行性变。