Literature DB >> 36261624

Formation and fate of an engram in the lateral amygdala supporting a rewarding memory in mice.

Albert Park1, Alexander D Jacob1,2, Hwa-Lin Liz Hsiang1, Paul W Frankland1,2,3,4, John G Howland5, Sheena A Josselyn6,7,8.   

Abstract

Memories allow past experiences to guide future decision making and behavior. Sparse ensembles of neurons, known as engrams, are thought to store memories in the brain. Most previous research has focused on engrams supporting threatening or fearful memories where results show that neurons involved in a particular engram ("engram neurons") are both necessary and sufficient for memory expression. Far less is understood about engrams supporting appetitive or rewarding memories. As circumstances and environments are dynamic, the fate of a previously acquired engram with changing circumstances is unknown. Here we examined how engrams supporting a rewarding cue-cocaine memory are formed and whether this original engram is important in reinstatement of memory-guided behavior following extinction. Using a variety of techniques, we show that neurons in the lateral amygdala are allocated to an engram based on relative neuronal excitability at training. Furthermore, once allocated, these neurons become both necessary and sufficient for behavior consistent with recall of that rewarding memory. Allocated neurons are also critical for cocaine-primed reinstatement of memory-guided behavior following extinction. Moreover, artificial reactivation of initially allocated neurons supports reinstatement-like behavior following extinction even in the absence of cocaine-priming. Together, these findings suggest that cocaine priming after extinction reactivates the original engram, and that memory-guided reinstatement behavior does not occur in the absence of this reactivation. Although we focused on neurons in one brain region only, our findings that manipulations of lateral amygdala engram neurons alone were sufficient to impact memory-guided behavior indicate that the lateral amygdala is a critical hub region in what may be a larger brain-wide engram.
© 2022. The Author(s), under exclusive licence to American College of Neuropsychopharmacology.

Entities:  

Year:  2022        PMID: 36261624     DOI: 10.1038/s41386-022-01472-5

Source DB:  PubMed          Journal:  Neuropsychopharmacology        ISSN: 0893-133X            Impact factor:   8.294


  53 in total

Review 1.  Memory Engram Cells Have Come of Age.

Authors:  Susumu Tonegawa; Xu Liu; Steve Ramirez; Roger Redondo
Journal:  Neuron       Date:  2015-09-02       Impact factor: 17.173

Review 2.  Finding the engram.

Authors:  Sheena A Josselyn; Stefan Köhler; Paul W Frankland
Journal:  Nat Rev Neurosci       Date:  2015-09       Impact factor: 34.870

Review 3.  Heroes of the Engram.

Authors:  Sheena A Josselyn; Stefan Köhler; Paul W Frankland
Journal:  J Neurosci       Date:  2017-05-03       Impact factor: 6.167

4.  Cortical representations are reinstated by the hippocampus during memory retrieval.

Authors:  Kazumasa Z Tanaka; Aleksandr Pevzner; Anahita B Hamidi; Yuki Nakazawa; Jalina Graham; Brian J Wiltgen
Journal:  Neuron       Date:  2014-10-09       Impact factor: 17.173

5.  Hippocampal memory traces are differentially modulated by experience, time, and adult neurogenesis.

Authors:  Christine A Denny; Mazen A Kheirbek; Eva L Alba; Kenji F Tanaka; Rebecca A Brachman; Kimberly B Laughman; Nicole K Tomm; Gergely F Turi; Attila Losonczy; René Hen
Journal:  Neuron       Date:  2014-07-02       Impact factor: 17.173

Review 6.  Still searching for the engram.

Authors:  Howard Eichenbaum
Journal:  Learn Behav       Date:  2016-09       Impact factor: 1.986

7.  Direct reactivation of a coherent neocortical memory of context.

Authors:  Kiriana K Cowansage; Tristan Shuman; Blythe C Dillingham; Allene Chang; Peyman Golshani; Mark Mayford
Journal:  Neuron       Date:  2014-10-09       Impact factor: 17.173

8.  Optogenetic stimulation of a hippocampal engram activates fear memory recall.

Authors:  Xu Liu; Steve Ramirez; Petti T Pang; Corey B Puryear; Arvind Govindarajan; Karl Deisseroth; Susumu Tonegawa
Journal:  Nature       Date:  2012-03-22       Impact factor: 49.962

9.  Orchestrated ensemble activities constitute a hippocampal memory engram.

Authors:  Khaled Ghandour; Noriaki Ohkawa; Chi Chung Alan Fung; Hirotaka Asai; Yoshito Saitoh; Takashi Takekawa; Reiko Okubo-Suzuki; Shingo Soya; Hirofumi Nishizono; Mina Matsuo; Makoto Osanai; Masaaki Sato; Masamichi Ohkura; Junichi Nakai; Yasunori Hayashi; Takeshi Sakurai; Takashi Kitamura; Tomoki Fukai; Kaoru Inokuchi
Journal:  Nat Commun       Date:  2019-06-14       Impact factor: 14.919

10.  Distinct hippocampal engrams control extinction and relapse of fear memory.

Authors:  Anthony F Lacagnina; Emma T Brockway; Chelsea R Crovetti; Francis Shue; Meredith J McCarty; Kevin P Sattler; Sean C Lim; Sofia Leal Santos; Christine A Denny; Michael R Drew
Journal:  Nat Neurosci       Date:  2019-04-01       Impact factor: 24.884

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