Environmental enrichment preserves a young DNA methylation landscape in the aged mouse hippocampus.
Sara ZocherRupert W OverallMatthias LescheAndreas DahlGerd KempermannPublished in: Nature communications (2021)
The decline of brain function during aging is associated with epigenetic changes, including DNA methylation. Lifestyle interventions can improve brain function during aging, but their influence on age-related epigenetic changes is unknown. Using genome-wide DNA methylation sequencing, we here show that experiencing a stimulus-rich environment counteracts age-related DNA methylation changes in the hippocampal dentate gyrus of mice. Specifically, environmental enrichment prevented the aging-induced CpG hypomethylation at target sites of the methyl-CpG-binding protein Mecp2, which is critical to neuronal function. The genes at which environmental enrichment counteracted aging effects have described roles in neuronal plasticity, neuronal cell communication and adult hippocampal neurogenesis and are dysregulated with age-related cognitive decline in the human brain. Our results highlight the stimulating effects of environmental enrichment on hippocampal plasticity at the level of DNA methylation and give molecular insights into the specific aspects of brain aging that can be counteracted by lifestyle interventions.
Keyphrases
- dna methylation
- cerebral ischemia
- genome wide
- subarachnoid hemorrhage
- cognitive decline
- gene expression
- blood brain barrier
- brain injury
- physical activity
- single cell
- human health
- copy number
- metabolic syndrome
- cardiovascular disease
- white matter
- mild cognitive impairment
- resting state
- binding protein
- weight loss
- risk assessment
- life cycle
- endothelial cells
- functional connectivity
- climate change
- oxidative stress
- type diabetes
- cell therapy
- stem cells
- skeletal muscle
- insulin resistance
- mesenchymal stem cells
- multiple sclerosis
- high glucose
- bone marrow