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McKenna, A. R.

Publications and source records attributed to McKenna, A. R..

2 recordsLinked to original sources

Aging disrupts transcriptional programs for memory updating in the dorsal hippocampus and reveals a required role for Tent5a in reconsolidation

Existing memories can be updated with new information through a process known as reconsolidation, though the molecular mechanisms underlying this process are poorly understood. Additionally, memory updating is impaired with aging, but little is known about how this impairment occurs. Here, we used a hippocampus-dependent memory updating task alongside transcriptomics to identify which genes are upregulated in the dorsal hippocampus specifically during a memory update in both young adult mice, which show successful memory updating, and in old mice, which do not. In young mice, we observed that distinct transcriptional programs were activated by reconsolidation-dependent memory updating and memory retrieval without new information. In old mice, similar transcriptional programs were engaged by both memory updating and memory retrieval. From our sequencing results, we identified Tent5a as a novel regulator of reconsolidation-mediated memory updating, and we demonstrate that hippocampal expression of Tent5a is necessary for this process. Together, these results expand our understanding of both the underlying transcriptional mechanisms of memory updating and how these mechanisms go awry in the aged brain.

neuroscience↗

Old mice fail to integrate a memory update into an existing hippocampal engram.

Existing memories can be updated by the presentation of new information during memory retrieval. Memory updating is impaired with age, and recent reports indicate this process is more susceptible to age-related impairments than the formation of new memories. However, the neuronal mechanisms underlying age-related updating impairments are unknown. Here, we investigated how memory engrams within the dorsal hippocampus encode a memory update in the young and old brain. We found that old mice tended to re-engage a smaller proportion of the original memory engram during the update session and chemogenetically increasing the activation of this engram alleviated age-related updating deficits. A range of therapeutically relevant behavioral and pharmacological approaches promoting re-engagement of the training engram also improved memory updating in old mice. Together, these results identify a novel mechanism by which memory updating is impaired with age and expand our understanding of how the brain organizes related information.

neuroscience↗