| Literature DB >> 32108298 |
Jung-Hyun Cho1,2, Seulah Lee1, Hyeyoung Jeon1, Ah Hyun Kim1, Wonjong Lee1, Yujeong Lee1, Seonguk Yang1, Jeanho Yun3, Young-Suk Jung1, Jaewon Lee4.
Abstract
Tetrabromobisphenol A (TBBPA) is widely used in materials like plastics and textiles as a fire retardant. In a previous study, we reported TBBPA might disrupt hippocampal neurogenesis and neurocognitive function in mice. However, the mechanism responsible for these effects has not been established. The present study was undertaken to investigate the potential involvement of oxidative stress and mitochondrial dysfunction in TBBPA-mediated neurotoxicity in neural stem cells. We confirmed TBBPA was more cytotoxic to neural stem cells than to neurons, astrocytes, or fibroblasts, and found that TBBPA-induced neural stem cell apoptosis was accompanied by increased reactive oxygen species generation and mitochondrial dysfunction. At a molecular level, TBBPA-induced apoptosis was determined to be mediated by c-Jun N-terminal kinase-p53 pathway activation. Taken together, these findings suggest that the adverse effects of TBBPA on hippocampal neurogenesis are due to the inhibition of neural stem cell expansion.Entities:
Keywords: Apoptosis; Mitochondria; Neural stem cell; Reactive oxygen species; TBBPA; c-Jun N-terminal kinase
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Year: 2020 PMID: 32108298 DOI: 10.1007/s12640-020-00179-z
Source DB: PubMed Journal: Neurotox Res ISSN: 1029-8428 Impact factor: 3.911