Increasing the GluN2A/GluN2B ratio in neurons of the mouse basal and lateral amygdala inhibits the modification of an existing fear memory trace

Roopashri Holehonnur, Aarron J. Phensy, Lily J. Kim, Milica Milivojevic, Dat Vuong, Delvin K. Daison, Saira Alex, Michael Tiner, Lauren E. Jones, Sven Kroener, Jonathan E. Ploski

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33 Scopus citations

Abstract

Reconsolidation updating is a form of memory modification in which an existing memory can become destabilized upon retrieval and subsequently be modified via protein-synthesis-dependent reconsolidation. However, not all memories appear to destabilize upon retrieval and thus are not modifiable via reconsolidation updating approaches and the neurobiological basis for this remains poorly understood. Here, we report that auditory fearmemoriescreated with10tone–shockpairings are resistant to retrieval-dependentmemorydestabilizationandare associated with an increase in the synaptic GluN2A/GluN2B ratio in neurons of the basal and lateral amygdala (BLA) compared with weaker fear memories created via one or three tone–shock pairings. To increase the GluN2A/GluN2B ratio after learning, we generated a line of mice that expresses an inducible and doxycycline-dependent GFP-GluN2A transgene specifically in α-CaMKII-positive neurons. Our findings indicate that increasing the GluN2A/GluN2B ratio inBLA α-CaMKII-positive neurons after a weak fear memory has consolidated inhibits retrieval-dependent memory destabilization and modification of the fearmemorytrace. This was associated with a reduction in retrieval-dependentAMPAreceptor trafficking, as evidenced by a reduction in retrieval-dependent phosphorylation of GluR1 at serine-845. In addition, we determined that increasing the GluN2A/GluN2B ratio before fear learning significantly impaired long term memory consolidation, whereas short-term memory remained unaltered. An increase in the GluN2A/GluN2B ratio after fear learning had no influence on fear extinction or expression. Our results underscore the importance of NMDAR subunit composition for memory destabilization and suggest a mechanism for why some memories are resistant to modification.

Original languageEnglish (US)
Pages (from-to)9490-9504
Number of pages15
JournalJournal of Neuroscience
Volume36
Issue number36
DOIs
StatePublished - Sep 7 2016

All Science Journal Classification (ASJC) codes

  • Neuroscience(all)

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