The research, by scientists at Harvard University, the University of California, Berkeley, Lawrence Berkeley National Laboratory, and the Max-Planck-Institute for Evolutionary Anthropology, will be reported this week in the open-access journal PLoS Biology.
"We were surprised both by the homogeneity of aging within the cortex and by the dramatic differences in aging between cortex and cerebellum," says Joshua B. Plotkin, a junior fellow in the Harvard Society of Fellows. "The fact that gene activity levels in the cerebellum remain more stable as a person ages suggests that this region of the brain experiences less oxidative stress and damage as part of normal aging."
"Much remains to be learned about how the brain ages and how changes in gene expression over time are related to brain activity," says Michael B. Eisen, assistant professor of molecular and cell biology at UC Berkeley. "Our analyses suggest that the different functions of different regions of the brain influence how they age, and that we can learn about functional variation and evolution by studying gene expression changes with age."
The researchers used data from gene chips to look at gene expression -- the degree to which various genes are turned "on" and "off" -- in five different regions of the brain's cortex. They found that in all five cortical areas, brain changes with aging were pronounced and consistent. Changes in gene expression in the cerebellum were smaller and less coordinated.
The study by Plotkin, Eisen, Berkeley graduate student Hunter B. Fraser, and Philipp Khaitovich and Svante Paabo from the Max-Planck-Institute in Leipzig, Germany, is one of many conducted to date on the question of how gene expression changes across the human lifespan, but the first to examine how the two major brain areas age differently. Scientists had also not previously compared the effects of aging on the brains of humans and other primates.
"The fact that chimpanzees' brains age so differently from our own suggests that our closest evolutionary relatives may use their brains very differently than we do," Plotkin says. "It appears that genome-wide patterns of aging evolve very rapidly."
The scientists say their results may cast some doubt on the effectiveness of mice and other species to model various types of neurodegenerative disease: If human and chimpanzee brains age in markedly dissimilar ways, the difference between humans and more distantly related species is likely greater yet.
This work was supported by the Bundesministerium fur Bildung und Forschung; the Burroughs Wellcome Fund; the William F. Milton Fund; the Pew Foundation; and the National Science Foundation.