Cited by 125Toxic Organic Pollutants ImpactEffects and risks of endocrine disrupting chemicalsCell death mechanisms and regulation

In vitro toxicity of Tetrabromobisphenol-A on cerebellar granule cells: cell death, free radical formation, calcium influx and extracellular glutamate

Reistad, T., Mariussen, E., Ring, A., Fonnum, F.·2006·Toxicological Sciences

Abstract

Tetrabromobisphenol-A (TBBPA) is one of the worlds most widely used brominated flame retardant. The present study reports effects of TBBPA on primary cultures of cerebellar granule cells (CGC). Using the trypan blue exclusion assay, we show that TBBPA induces death of CGC at low micro molar concentrations. Cell death was reduced by the NMDA receptor antagonist MK-801 (3 microM), the antioxidant vitamin E (50 microM), and in calcium-free buffer. We further demonstrate that TBBPA's toxicity was accompanied by apoptosis-like nuclear shrinkage, chromatin condensation, and DNA fragmentation. Other hallmarks of apoptosis such as caspase activity were, however, absent, indicating an atypical form of apoptosis. TBBPA increased intracellular free calcium in a concentration-dependent manner. TBBPA also induced an increase in extracellular glutamate in a time-dependent manner. TBBPA gave a concentration-dependent increase information reactive oxygen species (ROS) of measured with 2,7-dichlorofluorescein diacetate. The ROS formation was inhibited by the extracellular signal-regulated protein kinase (ERK) inhibitor U0126 (10 microM), the tyrosine kinase inhibitor erbstatin-A (25 microM), eliminating calcium from the buffer and by the superoxide dismutase inhibitor diethyldithio-carbamic acid (DDC, 100 microM). Further analysis with Western blot confirmed phosphorylation of ERK1/2 after exposure to TBBPA. We found that TBBPA induces ROS formation, increases intracellular calcium, extracell…

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Crossref · 10.1093/toxsci/kfl198

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  • TBBPA induces dose-dependent cytotoxicity in cerebellar granule cells, attributed to disturbed calcium currents together with increased oxidative stress.

    “TBBPA, for instance, induces dose-dependent cytotoxicity in cerebellar granule cells, an effect attributed to disturbed calcium currents together with increased oxidative stress (Al-Mousa and Michelangeli, 2014; Reistad et al., 2007; Zieminska et al., 2017).”

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Authors
Reistad, T., Mariussen, E., Ring, A., & Fonnum, F.
Affiliations
  • Norwegian Defence Research Establishment (NO)
  • NILU (NO)
  • University of Oslo (NO)
Corresponding author
Reistad, T.
Venue
Toxicological Sciences
Published
2006-10-31
Volume
96
Issue
2
Pages
268-278
ISSN
  • 1096-0929 (ISSN-L)
  • 1096-6080
OpenAlex
W2153466256
Cited by
125
References
1
Citations by year
2026: 2 · 2025: 2 · 2024: 5 · 2023: 4 · 2022: 7 · 2021: 5 · 2020: 6 · 2019: 8 · 2018: 7 · 2017: 12 · 2016: 10 · 2015: 9 · 2014: 5 · 2013: 9 · 2012: 7
FWCI
4.06
Type
journal article
Language
en
Open access
closed
Locations
  • Toxicological Sciences (publishedVersion)
  • PubMed (publishedVersion)
Funders
Norges Forskningsråd
Topics
  • Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Toxic Organic Pollutants Impact
  • Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Effects and risks of endocrine disrupting chemicals
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
Keywords
tetrabromobisphenol A, brominated flame retardants, cerebellar granule cells, neurotoxicity, apoptosis, reactive oxygen species, intracellular calcium, extracellular glutamate, ERK1/2 phosphorylation, NMDA receptor, vitamin E, caspase-independent cell death, environmental toxins
MeSH terms
Animals, Aspartic Acid, Calcium, Cell Nucleus, Cell Survival, Cells, Cultured, Cerebellum, Cytoplasmic Granules, Dose-Response Relationship, Drug, Enzyme Activation, Extracellular Space, Glutamates, Intracellular Fluid, Nucleosomes, Polybrominated Biphenyls, Protein-Tyrosine Kinases, Vitamin E, Hazardous Substances, Dizocilpine Maleate, Cell Death, Reactive Oxygen Species, Okadaic Acid, Caspases, Mitogen-Activated Protein Kinase 3, Rats, DNA Fragmentation, Caspase Inhibitors

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