4.7 Article

Maternal exposure to polystyrene nanoplastics causes brain abnormalities in progeny

期刊

JOURNAL OF HAZARDOUS MATERIALS
卷 426, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.jhazmat.2021.127815

关键词

Polystyrene nanoplastic; Generational transfer; Neurodevelopmental defects; Neural stem cell; Cognitive deficit

资金

  1. Korea Research Institute of Bioscience and Biotechnology (KRIBB) Initiative Research Program [KGM5222113, KGM5322113]
  2. National Research Foundation (NRF) - Ministry of Science and ICT (MSIT) [NRF-2019M3C7A1031534, NRF-2015M3C7A1029113, NRF-2019M3C7A1031742]
  3. NRF - Ministry of Ed-ucation [NRF-2019R1I1A2A01063642]
  4. NRF - MSIT [NRF-2019R1A2C2006740, NRF-2019R1A5A6099645, NRF-2019R1C1C1006084]
  5. National Research Council of Science & Technology (NST), Republic of Korea [KGM5322113, KGM5222113] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  6. National Research Foundation of Korea [2020R1A2C2006752, 2019M3C7A1031742, 2019M3C7A1031534] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

This study investigates the effects of polystyrene nanoplastic (PSNP) on the development of the central nervous system, and finds that exposure to high concentrations of PSNP may result in neurophysiological and cognitive deficits.
As global plastic production continues to grow, microplastics released from a massive quantity of plastic wastes have become a critical environmental concern. These microplastic particles are found in a wide range of living organisms in a diverse array of ecosystems. In this study, we investigated the biological effects of polystyrene nanoplastic (PSNP) on development of the central nervous system using cultured neural stem cells (NSCs) and mice exposed to PSNP during developmental stages. Our study demonstrates that maternal administration of PSNP during gestation and lactating periods altered the functioning of NSCs, neural cell compositions, and brain histology in progeny. Similarly, PSNP-induced molecular and functional defects were also observed in cultured NSCs in vitro. Finally, we show that the abnormal brain development caused by exposure to high concentrations of PSNP results in neurophysiological and cognitive deficits in a gender-specific manner. Our data demonstrate the possibility that exposure to high amounts of PSNP may increase the risk of neurodevelopmental defects.

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