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  2. Toxicogenomic assessment of hydroxylated metabolites of PBDEs on cetaceans: An in vitro study

Toxicogenomic assessment of hydroxylated metabolites of PBDEs on cetaceans: An in vitro study

  • Chemosphere. 2024 Oct:366:143350. doi: 10.1016/j.chemosphere.2024.143350.
Chengzhang Li 1 Ziyao Tian 1 Xinying Li 1 Yajing Sun 1 Jiashen Tian 2 Yuqi Wu 1 Jingting Cai 1 Yijie He 1 Edmond Sanganyado 3 Ping Li 1 Bo Liang 4 Wenhua Liu 5
Affiliations

Affiliations

  • 1 Guangdong Provincial Key Laboratory of Marine Disaster Prediction and Prevention, Guangdong Provincial Key Laboratory of Marine Biotechnology, Institute of Marine Sciences, Shantou University, Shantou, 515063, China.
  • 2 Dalian Key Laboratory of Conservation Biology for Endangered Marine Mammals, Liaoning Ocean and Fisheries Science Research Institute, Dalian, Liaoning, 116023, China.
  • 3 Department of Applied Sciences, Northumbria University, Newcastle upon Tyne, NE2 4PB, UK.
  • 4 Guangdong Provincial Key Laboratory of Marine Disaster Prediction and Prevention, Guangdong Provincial Key Laboratory of Marine Biotechnology, Institute of Marine Sciences, Shantou University, Shantou, 515063, China. Electronic address: liangbo@stu.edu.cn.
  • 5 Guangdong Provincial Key Laboratory of Marine Disaster Prediction and Prevention, Guangdong Provincial Key Laboratory of Marine Biotechnology, Institute of Marine Sciences, Shantou University, Shantou, 515063, China. Electronic address: whliu@stu.edu.cn.
Abstract

Despite their ban, polybrominated diphenyl ethers (PBDEs) are frequently detected in various environmental compartments including marine and coastal ecosystems due to their persistence, bio-accumulative, high production volumes, and widespread use. One of the major concerns from PBDEs is the transformation products, such as hydroxylated polybrominated diphenyl ethers (OH-BDEs), which are more bioactive than the parent compounds. For example, 6-hydroxy-2,2',4',4-tetrabromodiphenyl ether (6-OH-BDE-47) is a typical metabolite of PBDEs and cause endocrine system disruption, developmental toxicity, and neurotoxicity in different species. Despite being widely detected in marine environments, investigations on the toxicological mechanisms of 6-OH-BDE-47 in cetaceans remain scarce. High concentrations of PBDEs accumulate in cetaceans due to the long lifespan and large fat reserve. The accumulated PBDEs have become the major source of OH-BDEs in cetaceans. We exposed immortalized fibroblast cell lines from the skin of pygmy killer whales (PKW-LWHT) and Indo-Pacific finless porpoises (FP-LWHT) to 6-OH-BDE-47 and analyzed changes in cellular function using transcriptomic data, along with enzymatic activity. Exposure to the body-relevant body burdens of 6-OH-BDE-47 (250 and 500 ng mL-1) significantly decreased cell viability. Differentially expressed genes in FP-LWHT exposed to 6-OH-BDE-47 were primarily enriched in the pathways associated with steroid metabolism. Total Cholesterol was decreased by 6-OH-BDE-47, whereas low-density lipoprotein Cholesterol and triglyceride levels were significantly increased in FP-LWHT cells. In contrast, glycolysis was the main enriched function of differentially expressed genes in PKW-LWHT cells exposed to 6-OH-BDE-47, and the Enzyme activity of phosphofructokinase and Hexokinase was upregulated. Thus, even though the cell viability of both cell lines from these two species was significantly suppressed by 6-OH-BDE-47, the cellular response or affected cellular function was different between the Pygmy killer whale and the Indo-Pacific Finless Porpoise, suggesting a diverse response towards OH-BDEs exposure.

Keywords

Hydroxylated polybrominated diphenyl ethers (OH-BDEs); Porpoise; Pygmy killer whale; Skin fibroblast cell line.

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