Inhibition of histone lysine demethylase restores learning and memory in aged mice
Shail Ratna BhattiD, Lachlan Ford MacBean, Enikö A. KramáriD, Leticia Pérez‐SisquésiD, Phillip Smethurst, Josephine Louise RobbiD, Neeru JindaliD, Tracy L. FetterlyiD, Andrew Graham, Marcelo A. WoodiD, Sébastien GillotiniD, Karl-Peter GieseiD, M. Albert BassoniD
Abstract
Chromatin undergoes dramatic changes during the ageing process. In the brain, these chromatin changes are thought to underlie age-associated deficits in the activity-dependent gene transcription necessary for memory consolidation. Here, we show that the levels of a specific histone post-translational modification (PTM), trimethylation of lysine 4 on histone 3 (H3K4me3) is markedly increased in the hippocampus of aged mice and that the activity-induced increase in H3K4me3 that is observed in response to a learning stimulus in young mice, is severely blunted in the aged hippocampus. H3K4me3 typically marks open, accessible chromatin at the transcriptional start sites (TSSs) of actively transcribed genes. We identify altered H3K4me3 peaks at TSSs and show that ca. 90% of the activity-induced H3K4me3 changes at TSSs are either absent or reduced in the aged hippocampus. To understand the biological significance of these age-associated changes, we screened a library of pharmacological compounds for compounds that can alter H3K4me3 levels in hippocampal neurons. We show that treatment of aged mice with one of these, the LSD1 inhibitor ORY-1001, restored normal learning and memory in object location and recognition tasks. Furthermore, we show that ORY-1001 treatment increased long-term potentiation (LTP), a form of synaptic plasticity deficient in the aged hippocampus. These findings suggest that targeting the epigenetic machinery that regulates activity-dependent gene transcription may represent an avenue for treating age-associated cognitive impairment. HighlightsO_LIH3K4me3 levels are elevated in the naive aged mouse hippocampus C_LIO_LIActivity-dependent H3K4me3 induction is impaired in the aged mouse hippocampus C_LIO_LILSD1 inhibition restores learning and memory in aged mice C_LIO_LILSD1 inhibition restores activity-dependent Arc induction and increases LTP in the aged hippocampus C_LI O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=142 SRC="FIGDIR/small/695858v1_ufig1.gif" ALT="Figure 1"> View larger version (39K): org.highwire.dtl.DTLVardef@fccd92org.highwire.dtl.DTLVardef@11c4d93org.highwire.dtl.DTLVardef@128f8b8org.highwire.dtl.DTLVardef@e1341f_HPS_FORMAT_FIGEXP M_FIG C_FIG
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Organism
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- H3K4me3 enrichment defines neuronal age, while a youthful H3K27ac signature is recapitulated in aged neurons
Katherine A. Giles, Andrew J. Phipps, … Phillippa C. Taberlay·bioRxiv·Nov 11, 2021
- Leveraging unbiased LC-MS analysis to identify histone post-translational modifications associated with age-related decline of learning and memory
S. Bhatt, Hasini A. Kalpage, … Sébastien Gillotin·bioRxiv·Dec 9, 2025
- lncRNA Neat1 drives neuronal histone methylation and age-related memory impairments
Anderson A. Butler, Daniel R. Johnston, … Farah D. Lubin·Science SignalingPeer-reviewed·Jul 2, 2019
- Loss of H3K9 trimethylation leads to premature aging
Alejandro Ocampo, Calida Mrabti, … Yohan Bignon·bioRxiv·Jul 24, 2024
- Epigenetic regulation of the circadian gene Per1 in the hippocampus mediates age-related changes in memory and synaptic plasticity
Janine L. Kwapis, Yasaman Alaghband, … Marcelo A. Wood·bioRxiv·Apr 13, 2018
- Epigenetic derepression of H3K9me3 mitigates Alzheimer-related pathology and improves cognition via immunomodulation and Vgf induction
Dieu-Trang S. Fuchs, Jean‐Philippe Vit, … Maya Koronyo‐Hamaoui·bioRxiv·Oct 15, 2024