Human-made toxic chemicals that linger indefinitely in the environment disrupt the performance of critical helper cells in the mouse brain, leading to impaired function over long-term exposures, say neuroscientists at Georgetown University Medical Center.
Their study, believed to be the first to test polychlorinated biphenyls (PCBs) in astrocytes (cells that support neurons and are critical for homeostasis throughout the central nervous system) suggests that this persistent environmental toxicant could be a contributing factor in the development of neurodegenerative disorders. The findings were reported at the annual meeting of the Society for Neuroscience in Chicago.
The research, conducted in laboratory tests of mouse brain cells, shows how a once widely used mixture of PCBs turns on pathways in astrocytes that attempt to neutralise the toxins. Many antioxidant genes known to be relevant to neurodegeneration in humans are aberrantly activated in the mice cells, says the study’s lead researcher, Mondona McCann, a PhD candidate in Georgetown’s Interdisciplinary Program in Neuroscience.
“Our findings to-date show strong connections between these toxins and the health of astrocytes. They also contribute to our understanding of how crucial these astrocytes are to maintaining brain functioning,” says McCann.
These star-shaped cells maintain the blood-brain barrier, support neurons, regulate communication between neurons, and repair nervous tissue following injury, among many other supportive tasks. “If astrocytes fail, neurons die. They are key to maintaining homeostasis … physiological stability, throughout the brain,” she says.
PCBs are known to cause cancer, suppress the immune system, disrupt hormonal signals and impair reproduction. In post-mortem studies, they have also been correlated with the death of nigral brain cells (dopamine-producing cells) in patients with Parkinson’s disease.
PCBs were globally manufactured and widely used in the 20th century because the chemicals are stable, heat-resistant and electrically insulating, which made them ideal for use in coolants, flame retardants, lubricants, paints, adhesives and many other industrial products. However because of their toxicity, some countries began banning their use in the 1970s and 1980s. Worldwide production only ended in 2001.
The effect of these toxins continues, McCann says. “The same stability that made PCBs so useful has also made them persist in the environment.”
In addition to several human diseases, PCBs have recently been linked to the decline in the killer whale population; McCann suspects that a combination of environmental stressors such as PCBs and genetic predispositions are linked to neurodegeneration.
“People in certain regions are constantly exposed to a low dose of PCBs and other similar compounds for a long time over their lives,” McCann says. “Our lab findings suggest that such an accumulation can lead to oxidative stress in astrocytes, which could not then support the neurons they maintain.”
It is unlikely that we will ever be able to remove accumulated PCBs from a person, but if research in humans uncovers the specific pathways affected in the brain, “it may be possible to compensate clinically for the deficits seen in the functioning of astrocytes. We might be able to engage compensatory mechanisms to increase the cells’ capacity to buffer these toxicants and promote survival,” she says.
“This concept, that environmental stressors impinge on astrocyte health, is a fairly understudied area,” says Maguire-Zeiss.
This research was funded by a Medical Center Student Research Grant, a National Institutes of Health Neural Injury and Plasticity T32 training grant (5T32NS041218), and Georgetown’s Department of Neuroscience.
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