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Berdugo-Vega, G.

Publications and source records attributed to Berdugo-Vega, G..

3 recordsLinked to original sources

Hippocampal recruitment of cortical engrams underlies remote memory generalization

Time-dependent generalization of remote fear memories is generally viewed as a passive and progressive loss of contextual precision, yet its underlying mechanisms remain poorly understood. Here, we investigated the neurobiological correlates of remote generalization using a combination of engram and projection-specific manipulation technologies in mice. Our results show that remote fear generalization results in an increased recruitment of learning-associated engrams into recall ensembles in the medial prefrontal cortex (mPFC), a crucial brain area for remote memory storage. Moreover, we find that this recruitment, and concomitantly remote generalization, requires ventral hippocampal (vCA1) inputs conveying contextual information to the mPFC, for which activity of parvalbumin-expressing interneurons proves necessary. Together, our findings suggest that time-dependent fear generalization arises from active hippocampal-prefrontal circuit mechanisms rather than passive loss of contextual information.

neuroscience↗

De novo DNA methylation controls neuronal maturation during adult hippocampal neurogenesis

Dynamic DNA methylation controls gene-regulatory networks underlying cell fate specification. How DNA methylation patterns change during adult hippocampal neurogenesis and their relevance for adult neural stem cell differentiation and related brain function has, however, remained unknown. Here, we show that neurogenesis-associated de novo DNA methylation is critical for maturation and functional integration of adult-born hippocampal neurons. Cell stage-specific bisulfite sequencing revealed a pronounced gain of DNA methylation at neuronal enhancers, gene bodies and binding sites of pro-neuronal transcription factors during adult neurogenesis, which mostly correlated with transcriptional up-regulation of the associated loci. Inducible deletion of both de novo DNA methyltransferases Dnmt3a and Dnmt3b in adult neural stem cells specifically impaired dendritic outgrowth and synaptogenesis of new-born neurons, resulting in reduced hippocampal excitability and specific deficits in hippocampus-dependent learning and memory. Our results highlight that, during adult neurogenesis, remodeling of neuronal methylomes is fundamental for proper hippocampal function.

neuroscience↗

Adult-born neurons promote cognitive flexibility by improving memory precision and indexing

The dentate gyrus (DG) of the hippocampus is fundamental for cognitive flexibility and has the extraordinary ability to generate new neurons throughout life. Recent evidence suggested that adult-born neurons differentially modulate input to the DG during the processing of spatial information and novelty. However, how this differential regulation by neurogenesis is translated into different aspects contributing cognitive flexibility is unclear. Here, we increased adult-born neurons by a genetic expansion of neural stem cells and studied their influence during navigational learning. We found that increased neurogenesis improved memory precision, indexing and retention and that each of these gains was associated with a differential activation of specific DG compartments and better separation of memory representations in the DG-CA3 network. Our results highlight the role of adult-born neurons in promoting memory precision in the infrapyramidal and indexing in the suprapyramidal blade of the DG and together contributing to cognitive flexibility. One sentence summaryNeurogenesis improves memory precision and indexing.

neuroscience↗