Chronic pain Alters the Immune System.

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How Chronic Pain Alters the Immune System
Neuroscience NewsJanuary 28, 2016
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Epigenetics may bring us one step closer to better treatments for chronic pain.

Chronic pain may reprogram the way genes work in the immune system, according to a new study by McGill University researchers published in the journal Scientific Reports.

“We found that chronic pain changes the way DNA is marked not only in the brain but also in T cells, a type of white blood cell essential for immunity”, says Moshe Szyf, a professor in the Faculty of Medicine at McGill. “Our findings highlight the devastating impact of chronic pain on other important parts of the body such as the immune system.”

Chronic pain – pain that lasts six months or more — is one of the most common causes of disability worldwide. Despite enormous efforts to find new therapeutic strategies, however, effective treatments for chronic pain remain elusive.

Using rat models

The all-McGill team examined DNA from brains and white blood cells of rats, using a method that mapped DNA marking by a chemical called a methyl group. ”Methyl marks are important for regulating how these genes function,” explains co-author Laura Stone, a professor in Dentistry and researcher in the Alan Edwards Centre for Research on Pain. This sort of chemical marking is part of the growing field of epigenetics, which involves modifications that turn genes ‘on’ or ‘off’, effectively reprogramming how they work.
Image shows a broken DNA double helix.

The all-McGill team examined DNA from brains and white blood cells of rats, using a method that mapped DNA marking by a chemical called a methyl group. Image adapted from the McGill press release.

“We were surprised by the sheer number of genes that were marked by the chronic pain — hundreds to thousands of different genes were changed,” adds Szyf. “We can now consider the implications that chronic pain might have on other systems in the body that we don’t normally associate with pain.”

Possible targets for new pain medications

The findings could open new avenues to diagnosing and treating chronic pain in humans, the researchers suggest, as some of the genes found to be marked by chronic pain could also represent new targets for pain medications.
About this neuroscience research

Source: McGill University
Image Credit: The image is adapted from the McGill press release
Original Research: Full open access research for “Overlapping signatures of chronic pain in the DNA methylation landscape of prefrontal cortex and peripheral T cells” by Renaud Massart, Sergiy Dymov, Magali Millecamps, Matthew Suderman, Stephanie Gregoire, Kevin Koenigs, Sebastian Alvarado, Maral Tajerian, Laura Stone, and Moshe Szyf in Scientific Reports. Published online January 28 2016 doi:10.1038/srep19615

Abstract

Overlapping signatures of chronic pain in the DNA methylation landscape of prefrontal cortex and peripheral T cells

We tested the hypothesis that epigenetic mechanisms in the brain and the immune system are associated with chronic pain. Genome-wide DNA methylation assessed in 9 months post nerve-injury (SNI) and Sham rats, in the prefrontal cortex (PFC) as well as in T cells revealed a vast difference in the DNA methylation landscape in the brain between the groups and a remarkable overlap (72%) between differentially methylated probes in T cells and prefrontal cortex. DNA methylation states in the PFC showed robust correlation with pain score of animals in several genes involved in pain. Finally, only 11 differentially methylated probes in T cells were sufficient to distinguish SNI or Sham individual rats. This study supports the plausibility of DNA methylation involvement in chronic pain and demonstrates the potential feasibility of DNA methylation markers in T cells as noninvasive biomarkers of chronic pain susceptibility.

“Overlapping signatures of chronic pain in the DNA methylation landscape of prefrontal cortex and peripheral T cells” by Renaud Massart, Sergiy Dymov, Magali Millecamps, Matthew Suderman, Stephanie Gregoire, Kevin Koenigs, Sebastian Alvarado, Maral Tajerian, Laura Stone, and Moshe Szyf in Scientific Reports. Published online January 28 2016 doi:10.1038/srep19615
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