Vilaça Margarida, Esteves Telma, Seabra Rosária, Rocha Eduardo, Lopes Célia
Laboratory of Histology and Embryology, Department of Microscopy, ICBAS-School of Medicine and Biomedical Sciences, University of Porto, 4050-313 Porto, Portugal.
Team of Animal Morphology and Toxicology, CIIMAR/CIMAR-Interdisciplinary Centre of Marine and Environmental Research, University of Porto, 4450-208 Porto, Portugal.
J Xenobiot. 2025 Jun 1;15(3):84. doi: 10.3390/jox15030084.
Polycyclic aromatic hydrocarbons (PAHs), prevalent aquatic contaminants, arise from burning fossil fuels, a major source of greenhouse gases driving global warming. PAHs and warmer temperatures individually exert diverse negative effects on aquatic organisms. However, the effects of PAH exposure and/or rising temperature remain largely unknown. Liver in vitro models, like the rainbow trout () RTL-W1 liver cell line, have been employed to unravel PAH-exposure effects, primarily on cell viability and enzymatic activity. Here, monolayer-cultured (2D) RTL-W1 cells were used to assess the co-exposure effects of temperature (18 and 21 °C) and two PAHs, benzo[a]pyrene (B[a]P) and benzo[k]fluoranthene (B[k]F), at 10 and 100 nM. After a 72 h exposure, the cell density and viability were evaluated using the trypan blue and LDH assays. The mRNA levels of the detoxification-associated genes (), (), , (), (), (), and () were measured by RT-qPCR. Temperature influenced cell viability and LDH leakage. Both PAHs reduced the cell density and upregulated the mRNA levels of , , and , while and were only augmented after the higher B[k]F concentration. Temperature influenced and expression. There was no interaction between temperature and the PAHs. Overall, the results show that B[k]F has more effects on detoxification targets than B[a]P, whereas a temperature increase mildly affects gene expression. The RTL-W1 in 2D seems useful for unravelling not only the liver effects of PAH but also the impact of temperature stress.
多环芳烃(PAHs)是普遍存在的水生污染物,源自化石燃料燃烧,而化石燃料燃烧是导致全球变暖的温室气体的主要来源。PAHs和升高的温度分别对水生生物产生多种负面影响。然而,PAH暴露和/或温度升高的影响在很大程度上仍不为人知。肝脏体外模型,如虹鳟(Oncorhynchus mykiss)RTL-W1肝细胞系,已被用于揭示PAH暴露的影响,主要是对细胞活力和酶活性的影响。在这里,单层培养的(二维)RTL-W1细胞被用于评估温度(18和21°C)和两种PAHs,苯并[a]芘(B[a]P)和苯并[k]荧蒽(B[k]F)在10和100 nM浓度下的共同暴露影响。暴露72小时后,使用台盼蓝和LDH测定法评估细胞密度和活力。通过RT-qPCR测量解毒相关基因(CYP1A1、CYP1B1、UGT1A6、UGT1A7、UGT1A8、UGT1A9、GSTA1和GSTM1)的mRNA水平。温度影响细胞活力和LDH泄漏。两种PAHs均降低细胞密度并上调CYP1A1、CYP1B1和UGT1A6的mRNA水平,而只有在较高的B[k]F浓度后GSTA1和GSTM1才增加。温度影响UGT1A7和UGT1A8表达。温度和PAHs之间没有相互作用。总体而言,结果表明B[k]F对解毒靶点的影响比B[a]P更大,而温度升高对基因表达的影响较小。二维的RTL-W1似乎不仅有助于揭示PAH对肝脏的影响,还有助于揭示温度应激的影响。