Mice missing any of 11 genes involved in the immune response show brain changes that track with anxiety.
Researchers presented the unpublished findings yesterday at the 2017 Society for Neuroscience annual meeting in Washington, D.C.
“We know the immune response can have an effect on the brain,” says Shoshana Spring, project manager at the Mouse Imaging Centre at the Hospital for Sick Children in Toronto, Canada, who presented the work. “We wanted to know what type of effect it’s having.”
Spring and her colleagues used magnetic resonance imaging to measure the volumes of 104 brain regions in 11 strains of mice. (They studied at least 15 males and 15 females from each strain.)
The strains each lack one of 11 genes that play a role in immunity.
Some of the genes encode molecules called interleukins, which can either promote or dampen inflammation. One such molecule, interleukin-6, has been implicated in autism. Other genes, such as CD4 and CD8, characterize T cells, which protect the body from invaders.
All 11 strains show brain abnormalities, the researchers found. But the location and severity of the abnormalities vary widely.
Six of the strains show signs of anxiety; the other five strains do not. When the researchers grouped the strains based features of anxiety, patterns of brain volume abnormalities emerged.
The six strains that have anxiety features show alterations in the amygdala, which processes fear, and the hippocampus, which is involved in memory. These changes are consistent across the sexes. Both regions have been implicated in anxiety and autism, which often co-occur.
“Neuroanatomy is affected by the genetics, and it’s affected in a way that’s consistent with the behavior,” says Darren Fernandes, a graduate student in Jason Lerch’s lab at the University of Toronto, who helped to analyze the data.
The findings suggest neuroanatomy is a “middle ground” between genetics and behavior, Fernandes says. Researchers could use a similar approach to identify brain changes associated with behavioral features in mouse models of autism.
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