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Spatial Memory Engram in the Mouse Retrosplenial Cortex

Memory relies on lasting adaptations of neuronal properties elicited by stimulus-driven plastic changes [1]. The strengthening (and weakening) of synapses results in the establishment of functional ensembles. It is presumed that such ensembles (or engrams) are activated during memory acquisition and...

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Autores principales: Milczarek, Michal M., Vann, Seralynne D., Sengpiel, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6013279/
https://www.ncbi.nlm.nih.gov/pubmed/29887312
http://dx.doi.org/10.1016/j.cub.2018.05.002
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author Milczarek, Michal M.
Vann, Seralynne D.
Sengpiel, Frank
author_facet Milczarek, Michal M.
Vann, Seralynne D.
Sengpiel, Frank
author_sort Milczarek, Michal M.
collection PubMed
description Memory relies on lasting adaptations of neuronal properties elicited by stimulus-driven plastic changes [1]. The strengthening (and weakening) of synapses results in the establishment of functional ensembles. It is presumed that such ensembles (or engrams) are activated during memory acquisition and re-activated upon memory retrieval. The retrosplenial cortex (RSC) has emerged as a key brain area supporting memory [2], including episodic and topographical memory in humans [3, 4, 5], as well as spatial memory in rodents [6, 7]. Dysgranular RSC is densely connected with dorsal stream visual areas [8] and contains place-like and head-direction cells, making it a prime candidate for integrating navigational information [9]. While previous reports [6, 10] describe the recruitment of RSC ensembles during navigational tasks, such ensembles have never been tracked long enough to provide evidence of stable engrams and have not been related to the retention of long-term memory. Here, we used in vivo 2-photon imaging to analyze patterns of activity of over 6,000 neurons within dysgranular RSC. Eight mice were trained on a spatial memory task. Learning was accompanied by the gradual emergence of a context-specific pattern of neuronal activity over a 3-week period, which was re-instated upon retrieval more than 3 weeks later. The stability of this memory engram was predictive of the degree of forgetting; more stable engrams were associated with better performance. This provides direct evidence for the interdependence of spatial memory consolidation and RSC engram formation. Our results demonstrate the participation of RSC in spatial memory storage at the level of neuronal ensembles.
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spelling pubmed-60132792018-06-25 Spatial Memory Engram in the Mouse Retrosplenial Cortex Milczarek, Michal M. Vann, Seralynne D. Sengpiel, Frank Curr Biol Article Memory relies on lasting adaptations of neuronal properties elicited by stimulus-driven plastic changes [1]. The strengthening (and weakening) of synapses results in the establishment of functional ensembles. It is presumed that such ensembles (or engrams) are activated during memory acquisition and re-activated upon memory retrieval. The retrosplenial cortex (RSC) has emerged as a key brain area supporting memory [2], including episodic and topographical memory in humans [3, 4, 5], as well as spatial memory in rodents [6, 7]. Dysgranular RSC is densely connected with dorsal stream visual areas [8] and contains place-like and head-direction cells, making it a prime candidate for integrating navigational information [9]. While previous reports [6, 10] describe the recruitment of RSC ensembles during navigational tasks, such ensembles have never been tracked long enough to provide evidence of stable engrams and have not been related to the retention of long-term memory. Here, we used in vivo 2-photon imaging to analyze patterns of activity of over 6,000 neurons within dysgranular RSC. Eight mice were trained on a spatial memory task. Learning was accompanied by the gradual emergence of a context-specific pattern of neuronal activity over a 3-week period, which was re-instated upon retrieval more than 3 weeks later. The stability of this memory engram was predictive of the degree of forgetting; more stable engrams were associated with better performance. This provides direct evidence for the interdependence of spatial memory consolidation and RSC engram formation. Our results demonstrate the participation of RSC in spatial memory storage at the level of neuronal ensembles. Cell Press 2018-06-18 /pmc/articles/PMC6013279/ /pubmed/29887312 http://dx.doi.org/10.1016/j.cub.2018.05.002 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Milczarek, Michal M.
Vann, Seralynne D.
Sengpiel, Frank
Spatial Memory Engram in the Mouse Retrosplenial Cortex
title Spatial Memory Engram in the Mouse Retrosplenial Cortex
title_full Spatial Memory Engram in the Mouse Retrosplenial Cortex
title_fullStr Spatial Memory Engram in the Mouse Retrosplenial Cortex
title_full_unstemmed Spatial Memory Engram in the Mouse Retrosplenial Cortex
title_short Spatial Memory Engram in the Mouse Retrosplenial Cortex
title_sort spatial memory engram in the mouse retrosplenial cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6013279/
https://www.ncbi.nlm.nih.gov/pubmed/29887312
http://dx.doi.org/10.1016/j.cub.2018.05.002
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