1. Exposure to human relevant mixtures of halogenated persistent organic pollutants (POPs) alters neurodevelopmental processes in human neural stem cells undergoing differentiation
- Author
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Francesca Pistollato, Ragnhild E. Paulsen, Anna Bal-Price, Erik Ropstad, Hubert Dirven, Donatella Carpi, Hanne Friis Berntsen, Nichlas Davidsen, Anna Jacobsen Lauvås, Emilio Mendoza-de Gyves, and Oddvar Myhre
- Subjects
genetic structures ,Halogenation ,Neurite ,Human neural stem cells ,Synaptogenesis ,Gene Expression ,010501 environmental sciences ,Toxicology ,behavioral disciplines and activities ,01 natural sciences ,Article ,03 medical and health sciences ,Neural Stem Cells ,Pregnancy ,Adverse Outcome Pathway ,Neurites ,medicine ,Humans ,reproductive and urinary physiology ,Aryl hydrocarbon receptor ,030304 developmental biology ,0105 earth and related environmental sciences ,0303 health sciences ,Mathematical modelling ,biology ,urogenital system ,Chemistry ,Brain-Derived Neurotrophic Factor ,Persistent organic pollutants ,Neurite outgrowth ,In vitro toxicology ,Neurotoxicity ,Brain ,Cell Differentiation ,Human brain ,Models, Theoretical ,medicine.disease ,Neural stem cell ,Cell biology ,medicine.anatomical_structure ,Receptors, Aryl Hydrocarbon ,Neurodevelopmental Disorders ,Prenatal Exposure Delayed Effects ,Synapses ,biology.protein ,Female ,Developmental neurotoxicity - Abstract
Highlights • Mixtures of 29 halogenated POPs were reconstructed based on human blood levels. • In vitro assays permitted to evaluate DNT effects in human iPSC-derived NSCs. • POPs at human blood levels increased proliferating NSCs and decreased synapses. • Mathematical modelling showed that synaptogenesis was the most sensitive DNT endpoint. • Data support a possible link between POPs and neurodevelopmental disorders., Halogenated persistent organic pollutants (POPs) like perfluorinated alkylated substances (PFASs), brominated flame retardants (BFRs), organochlorine pesticides and polychlorinated biphenyls (PCBs) are known to cause cancer, immunotoxicity, neurotoxicity and interfere with reproduction and development. Concerns have been raised about the impact of POPs upon brain development and possibly neurodevelopmental disorders. The developing brain is a particularly vulnerable organ due to dynamic and complex neurodevelopmental processes occurring early in life. However, very few studies have reported on the effects of POP mixtures at human relevant exposures, and their impact on key neurodevelopmental processes using human in vitro test systems. Aiming to reduce this knowledge gap, we exposed mixed neuronal/glial cultures differentiated from neural stem cells (NSCs) derived from human induced pluripotent stem cells (hiPSCs) to reconstructed mixtures of 29 different POPs using concentrations comparable to Scandinavian human blood levels. Effects of the POP mixtures on neuronal proliferation, differentiation and synaptogenesis were evaluated using in vitro assays anchored to common key events identified in the existing developmental neurotoxicity (DNT) adverse outcome pathways (AOPs). The present study showed that mixtures of POPs (in particular brominated and chlorinated compounds) at human relevant concentrations increased proliferation of NSCs and decreased synapse number. Based on a mathematical modelling, synaptogenesis and neurite outgrowth seem to be the most sensitive DNT in vitro endpoints. Our results indicate that prenatal exposure to POPs may affect human brain development, potentially contributing to recently observed learning and memory deficits in children.
- Published
- 2021
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