4.6 Article

Hydroxylated and sulfated metabolites of commonly observed airborne polychlorinated biphenyls display selective uptake and toxicity in N27, SH-SY5Y, and HepG2 cells

Journal

ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY
Volume 62, Issue -, Pages 69-78

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.etap.2018.06.010

Keywords

PCB; Hydroxy PCB; OH-PCB; PCB sulfate; Neurotoxicity; Hepatotoxicity

Funding

  1. NIH from the National Institute of Environmental Health Sciences [P42 ES013661]
  2. University of Iowa Environmental Health Sciences Research Center [NIEHS/NIH P30 ES05605]
  3. NATIONAL CANCER INSTITUTE [P30CA086862] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES [P42ES013661, P30ES005605] Funding Source: NIH RePORTER

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Although neurotoxicity and hepatotoxicity have long been associated with exposure to polychlorinated biphenyls (PCBs), less is known about the selective toxicity of those hydroxylated PCBs (OH-PCBs) and PCB sulfates that are metabolites derived from exposure to PCBs found in indoor air. We have examined the toxicity of OH PCBs and PCB sulfates derived from PCBs 3, 8, 11, and 52 in two neural cell lines (N27 and SH-SY5Y) and an hepatic cell line (HepG2). With the exception of a similar toxicity seen for N27 cells exposed to either OH-PCB 52 or PCB 52 sulfate, these OH-PCBs were more toxic to all three cell-types than their corresponding PCB or PCB sulfate congeners. Differences in the distribution of individual OH-PCB and PCB sulfate congeners between the cells and media, and the ability of cells to interconvert PCB sulfates and OH-PCBs, were important components of cellular sensitivity to these toxicants.

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