Vol. 118, No. 4 NewsOpen AccessBrain Drain? PBDEs Alter Development of Human Brain Cells Kellyn S. Betts Kellyn S. Betts Search for more papers by this author Published:1 April 2010https://doi.org/10.1289/ehp.118-a173aCited by:1AboutSectionsPDF ToolsDownload CitationsTrack Citations ShareShare onFacebookTwitterLinked InReddit A new laboratory study demonstrating that polybrominated diphenyl ethers (PBDEs) can alter human fetal brain cells may explain at least in part the neurotoxicity recently documented in epidemiologic studies of young children exposed to PBDEs and previously shown in animal models [EHP118:572–578; Schreiber et al.]. The new study, the first to examine PBDE neurotoxicity in a human cell–based system, links the brain cell alterations to endocrine disruption.A wealth of data demonstrates that babies can be exposed to significant amounts of PBDE flame retardants both in the womb and through breastfeeding. Although all 3 PBDE formulations—penta, octa, and deca—are banned in Europe, and the penta and octa formulations were discontinued in the United States (deca also is banned in some states), PBDEs may still be used in some new U.S. products and in wares manufactured elsewhere. They also are found in a wide variety of older plastic consumer goods that remain in use in many homes, businesses, and automobiles. The PBDEs are known to migrate into indoor dust, posing a particularly high exposure risk to infants and toddlers because of their characteristic hand-to-mouth behavior.To investigate how PBDEs may impact the developing fetal brain, the team of scientists employed a method for evaluating human developmental neurotoxicity they had recently developed [EHP 117:1131–1138] as an alternative to animal testing. This method uses primary fetal human neural progenitor cells (hNPCs) cultured to produce complex 3-dimensional cellular systems called neurospheres. Neurospheres undergo the same basic processes that occur during the early stages of normal human brain development: cell proliferation, differentiation, and migration. Tests conducted with neurospheres may help identify exogenous substances that disturb these basic processes in vivo.The researchers focused on 2 of the PBDE compounds that accumulate the most in humans, BDE-47 and BDE-99. At concentrations below levels that cause cell death, they found these compounds could reduce the migration of the hNPCs—which suggests the possibility of adverse effects on brain development—and the effects increased with higher PBDE concentrations. At the highest tested concentration (10 μM), BDE-47 decreased the distance the cells migrated by more than 25% compared with unexposed cells, whereas the same concentration of BDE-99 decreased the distance by more than 30%. Additional testing established that both compounds also interfered with the differentiation of immature progenitor cells into neurons and oligodendrocytes.Further tests suggested the PBDE compounds affected cell migration and differentiation by interfering with thyroid hormone signaling, an endocrine-disrupting effect that could be associated with additional impacts throughout a person’s life. Followup work to determine whether PBDEs cause the same effects in rodent neurospheres would facilitate extrapolation from animals to humans, the authors say.Other work has shown the tendency of PBDEs to accumulate in brain and neuronal cells, and the researchers used radiolabeled BDE-47 to measure an accumulation in test cells of approximately 60-fold. Considered with available human exposure data, these data suggest current PBDE exposure levels are likely to be of concern for human health, the authors write. Two recent studies have linked PBDEs with subtle changes in childrens’ IQs and behavior [EHP 117:1953–1958 and EHP doi:10.1289/ehp.0901340], and the authors say additional studies are needed to assess these associations.This fluorescence micrograph of differentiated neural progenitor cells shows neurons in green, glial cells in red, and cell nuclei in deep blue (the turquoise results from the overlay of the blue and green channels).FiguresReferencesRelatedDetailsCited by Akbar M, Narayanan S, Restaino M and Agah M (2014) A purge and trap integrated microGC platform for chemical identification in aqueous samples, The Analyst, 10.1039/C4AN00254G, 139:13, (3384-3392) Vol. 118, No. 4 April 2010Metrics About Article Metrics Publication History Originally published1 April 2010Published in print1 April 2010 Financial disclosuresPDF download License information EHP is an open-access journal published with support from the National Institute of Environmental Health Sciences, National Institutes of Health. All content is public domain unless otherwise noted. Note to readers with disabilities EHP strives to ensure that all journal content is accessible to all readers. However, some figures and Supplemental Material published in EHP articles may not conform to 508 standards due to the complexity of the information being presented. If you need assistance accessing journal content, please contact [email protected]. Our staff will work with you to assess and meet your accessibility needs within 3 working days.
Search from 250 M+ research papersSearch from 250 M+ research papers
Open Access
Jul 11, 2023
D.R Juberg + 9
