Just two hours of exposure to diesel exhaust fumes can lead to fundamental health-related changes in biology by switching some genes on, while switching others off, according to researchers at the University of British Columbia (UBC) and Vancouver Coastal Health.
The study involved putting volunteers in a polycarbonate-enclosed booth — about the size of a standard bathroom — while breathing in diluted and aged exhaust fumes that are about equal to the air quality along a Beijing highway, or under certain conditions at busy ports, rail yards, mines and industrial sites.
The researchers examined how such exposure affected the chemical “coating” that attaches to many parts of a person’s DNA. That carbon-hydrogen coating, called methylation, can silence or dampen a gene, preventing it from producing a protein – sometimes to a person’s benefit, sometimes not. Methylation is one of several mechanisms for controlling gene expression, which is the focus of a rapidly growing field of study called epigenetics.
The study found that diesel exhaust caused changes in methylation at about 2,800 different points on people’s DNA, affecting about 400 genes. In some places it led to more methylation; in more cases, it decreased methylation.
How these changes in gene expression translate to health is the next step for researchers. But this study shows how vulnerable our genetic machinery can be to air pollution, and that changes are taking place even if there are no obvious symptoms.
“Usually when we look at the effects of air pollution, we measure things that are clinically obvious – air flow, blood pressure, heart rhythm,” said senior author Chris Carlsten, an associate professor in UBC's Division of Respiratory Medicine. “But asthma, higher blood pressure or arrhythmia might just be the gradual accumulation of epigenetic changes. So we’ve revealed a window into how these long-term problems arise. We’re looking at changes ‘deep under the hood.’”
The fact that DNA methylation was affected after only two hours of exposure has positive implications, said Carlsten, the AstraZeneca chair in occupational and environmental lung disease.
“Any time you can show something happens that quickly, it means you can probably reverse it – either through a therapy, a change in environment, or even diet,” he said.
Carlsten’s team, having catalogued the changes along the entire human genome, is now sharing its data with scientists who are further exploring the function of specific genes.
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