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van den Oever, M.

Publications and source records attributed to van den Oever, M..

2 recordsLinked to original sources

Distributed neuronal ensembles support episodic-like memory retrieval

Memory is proposed to depend on neuronal ensembles distributed across multiple brain regions, yet how episodic-like memories are organized across the brain remains unclear. Here we investigated the brain-wide organization of object-place-context (OPC) memory in mice. By mapping c-Fos activation across the brain during memory recall and comparing it to multiple control conditions, we identified a set of brain regions selectively engaged during episodic-like memory retrieval, consistent with the recruitment of a fronto-posterior medial network. Chemogenetic manipulation of learning-activated neuronal ensembles revealed that the selected brain regions are necessary for memory retrieval. Within this network, the retrosplenial cortex emerged as a key region required for successful memory recall, with neuronal ensembles exhibiting properties of engram cells. Electrophysiological recordings during recall revealed distinct novelty-related dynamics across regions. In mPFC, theta power increased during novel exploration, while firing rate increased both immediately before and during interaction with the novel object configuration. In RSP, novelty was associated with a sharp increase in firing rate during exploration. Together, our findings suggest a distributed organization supporting episodic-like memory retrieval in mice, in which a posterior-medial network is activated and necessary for a successful behavioral expression.

neuroscience↗

Progressive remote memory decline coincides with parvalbumin interneuron hyperexcitability and enhanced inhibition of cortical engram cells in a mouse model of Alzheimers disease

Patients with Alzheimers disease (AD) initially show temporally-graded retrograde amnesia, which gradually progresses into more severe retrograde amnesia. Although mouse models of AD have provided insight into neurobiological mechanisms contributing to impaired formation and retrieval of new memories, the process underlying the progressive loss of remote memories in AD has remained elusive. Here, we demonstrate age-dependent remote memory decline in APP/PS1 mice, which coincides with progressive hyperexcitability of parvalbumin (PV) interneurons in the medial prefrontal cortex (mPFC). Analysis of Fos expression showed that the remote memory deficit is not mirrored by changes in reactivation of memory-encoding neurons, so-called engram cells, nor PV interneuron (re)activation, in the mPFC. However, inhibitory input is enhanced onto engram cells compared to non-engram cells specifically in APP/PS1 mice. Our data indicate that age-dependent remote memory impairment in APP/PS1 mice is due to increased innervation of cortical engram cells by hyperexcitable PV interneurons, suggesting that dysfunctional inhibitory microcircuits in the neocortex mediate progressive retrograde amnesia in AD.

neuroscience↗