Ortho-substituted PCB 153: effects in CHO-K1 cells

Author:

Miletić Marina1,Murati Teuta1,Šimić Branimir1,Bilandžić Nina2,Brozović Anamaria3,Kmetič Ivana1

Affiliation:

1. 1 University of Zagreb Faculty of Food Technology and Biotechnology, Laboratory for Toxicology , Zagreb , Croatia

2. 2 Croatian Veterinary Institute , Department of Veterinary Public Health, Laboratory for Residue Control , Zagreb , Croatia

3. 3 Ruđer Bošković Institute, Division of Molecular Biology, Laboratory for Cell Biology and Signalling , Zagreb , Croatia

Abstract

Abstract Non-planar di-ortho-substituted PCB 153 (2,2’,4,4’,5,5’-hexachlorobiphenyl), one of the most abundant PCB congeners in the environment and in biological and human tissues, has been identified as potential endocrine disruptor affecting the reproductive and endocrine systems in rodents, wildlife, and humans. The aim of this study was to gain a deeper insight into its mode/mechanism of action in Chinese hamster ovary K1 cells (CHO-K1). PCB 153 (10–100 μmol/L) inhibited CHO-K1 cell proliferation, which was confirmed with four bioassays (Trypan Blue, Neutral Red, Kenacid Blue, and MTT), of which the MTT assay proved the most sensitive. PCB 153 also induced ROS formation in a dose-dependent manner. Apoptosis was seen after 6 h of exposure to PCB 153 doses ≥50 μmol/L, while prolonged exposure resulted in the activation of the necrotic pathway. PCB 153-induced disturbances in normal cell cycle progression were time-dependent, with the most significant effects occurring after 72 h.

Publisher

Walter de Gruyter GmbH

Subject

Public Health, Environmental and Occupational Health,Toxicology

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