Summary: Researchers have discovered that age-related cognitive decline is most pronounced in the brain’s white matter, crucial for signal transmission.
This study in mice sheds light on aging’s contribution to neurodegenerative conditions like Alzheimer’s and Parkinson’s. Additionally, interventions such as plasma infusions from younger mice appear to slow this decline.
These findings pave the way for further research into human brain aging and potential therapies.
White matter in the brain, responsible for transmitting signals, showed the earliest and most significant age-related gene expression changes in mice.
Plasma infusions from young mice seem to reverse some age-related gene expression, offering potential as a treatment against cognitive decline.
The study provides insights into the vulnerability of specific brain regions to neurodegenerative diseases and how aging might exacerbate them.
Most of us who’ve reached middle age have noticed a slowing in memory and cognition, but scientists don’t have a clear picture of the molecular changes that take place in the brain to cause it.
Now, a study in mice has determined that the most pronounced changes occur in the white matter, a type of nervous system tissue that’s integral to transmitting signals across the brain.
The study also examined two treatments — caloric restriction and infusions of plasma from young mice — that affect certain regions of the brain, with the plasma appearing to slow the age-related decline.
The results offer insight into the cognitive decline of normal aging, as well as the way aging contributes to neurodegenerative conditions such as Alzheimer’s and Parkinson’s diseases and multiple sclerosis.
In many neurodegenerative diseases, certain areas of the brain are more vulnerable to damage, but scientists don’t know exactly why.
“I saw this study as a way to explain that somewhat mysterious regional vulnerability,” said Tony Wyss-Coray, PhD, a professor of neurology and neurological sciences who led the study that examined gene expression in different regions of the mouse brain as it matures.
Wyss-Coray, the D.H. Chen Professor II at Stanford Medicine and the director of the Phil and Penny Knight Initiative for Brain Resilience at Stanford’s Wu Tsai Neurosciences Institute, is the senior author of a paper describing the research. Oliver Hahn, formerly a postdoctoral fellow in the Wyss-Coray lab and now a principal investigator at Calico Life Sciences, is the lead author on the paper.
The paper was published Aug. 16 in Cell.
Different genes found in different regions
The research team sampled 15 regions in both hemispheres of the brains of 59 female and male mice aged 3 to 27 months. They identified and ranked the top genes expressed by cells found in each region of the brain. They identified 82 genes that are frequently found and vary in concentration in 10 or more regions.
The team used these genes to develop a common aging score, assessing how gene activity in different regions of the brain change with age.
The researchers found that the white matter, which is found deep in the brain and contains nerve fibers protected by white-colored myelin, showed the earliest and most pronounced changes in gene expression for mice 12 and 18 months old. According to Wyss-Coray, these mice are about as old, in mouse years, as a person in their 50s.
“We cannot definitively say how gene expression changes in white matter affect memory and cognition. That would require more genetic manipulation and neurobiology work,” Wyss-Coray said.
“But we knowwhite matter is the wiring that connects the different brain regions together.”
Past work has shown that aging disrupts an otherwise stable gene expression pattern in the brain, turning on genes that regulate inflammation and the immune response, and turning off genes responsible for protein and collagen synthesis.
The inflammation and immune response affect the integrity of the myelin sheath, the insulation layer around nerves responsible for transmitting signals across the brain.
“White matter has been a rather neglected area in aging research, which usually focuses on the neuron-dense regions like the cortex or hippocampus,” Hahn said. “The fact that white matter is emerging in our data as an area of particular vulnerability to aging opens up new and intriguing hypotheses.”
Interventions to slow the genetic shift that leads to the decline in specific regions of the brain could be beneficial in addressing neurodegenerative disease as well as the general decline associated with aging.
During the study, the team explored two interventions — carloric restriction and injections of plasma from young mice — to evaluate whether they protected against the region-specific shifts in gene expression. Each intervention began when the mice were 19 months old and lasted four weeks.
The researchers found that the dietary intervention caused genes associated with circadian rhythms to turn on, while the plasma intervention turned on genes involved in stem cell differentiation and neuronal maturation that led to selective reversal of age-related gene expression.
“The interventions appeared to act on very different regions in the brain and [induce] strikingly different effects,” Hahn said. “This suggests that there are multiple regions and pathways in the brain that have the potential to improve cognitive performance at old age.”
The team also examined age-related changes in genes associated with three neurodegenerative diseases — Alzheimer’s disease, Parkinson’s disease and multiple sclerosis — that typically affect specific regions of the brain.
The expression distribution for each gene had changed in older animals and occurred in regions of the brain that are not typically associated with a particular neurodegenerative condition.
This finding could offer insight into the vast number of patients who have neurodegenerative diseases without a firm genetic link.
The study could also offer new opportunities to explore treatments and interventions by using the gene expression data to zero in on the cell populations vulnerable to aging.
Future studies could explore how gene expression leads to functional changes in neuronal activity and structure. Wyss-Coray and colleagues at the Knight Initiative for Brain Resilience aim to expand on this work by building similar genetic atlases of aging in the human brain.
“The individual gene changes observed in the mouse may not directly translate to humans,” Wyss-Coray said. “But we believe the vulnerability of white matter to aging probably does.”
Researchers at New York University Langone Health, Saarland University, the Helmholtz-Centre for Infection Research, the Max Planck Institute for Biology of Ageing, Alkahest Inc. and University College London contributed to the study.
Funding: This study received funding from the Phil and Penny Knight Initiative for Brain Resilience, the European Research Council, the Max Planck Society, the Schaller-Nikolich Foundation, the Wu Tsai Neurosciences Institute and Foundation Bertarelli, the Simons Foundation, the Cure Alzheimer’s Fund, the National Institute of Aging, the Milky Way Research Foundation, the American Heart Association-Allen Initiative in Brain Health and Cognitive Impairment, and the Michael J. Fox Foundation for Parkinson’s Research.
About this neuroscience and brain aging research news
Author: Margarita Gallardo Source: Stanford Contact: Margarita Gallardo – Stanford Image: The image is credited to Neuroscience News
Atlas of the aging mouse brain reveals white matter as vulnerable foci
Brain-wide gene signature of aging in glial cells with spatially defined changes
Glial cell aging is accelerated in white matter
Rejuvenation interventions have region-specific effects on gene expression
Genes implicated in neurodegenerative diseases show regional aging patterns
Aging is the key risk factor for cognitive decline, yet the molecular changes underlying brain aging remain poorly understood. Here, we conducted spatiotemporal RNA sequencing of the mouse brain, profiling 1,076 samples from 15 regions across 7 ages and 2 rejuvenation interventions.
Our analysis identified a brain-wide gene signature of aging in glial cells, which exhibited spatially defined changes in magnitude.
By integrating spatial and single-nucleus transcriptomics, we found that glial aging was particularly accelerated in white matter compared with cortical regions, whereas specialized neuronal populations showed region-specific expression changes.
Rejuvenation interventions, including young plasma injection and dietary restriction, exhibited distinct effects on gene expression in specific brain regions.
Furthermore, we discovered differential gene expression patterns associated with three human neurodegenerative diseases, highlighting the importance of regional aging as a potential modulator of disease.
Our findings identify molecular foci of brain aging, providing a foundation to target age-related cognitive decline.