Abstract
Memories are encoded within sparsely distributed neuronal ensembles. However, the defining cellular properties of neurons within a memory trace remain incompletely understood Using a fluorescence-based Arc reporter, we were able to visually identify the distinct subset of lateral amygdala (LA) neurons activated during auditory fear conditioning. kAte found that Arc-expressing neurons have enhanced intrinsic excitability and are preferentially recruited into newly encoded memory traces. Furthermore, synaptic potentiation of thalamic inputs to the LA during fear conditioning is learning-specific, postsynaptically mediated and highly localized to Arc-expressing neurons. Taken together, our findings validate the immediate-early gene Arc as a molecular marker for the LA neuronal ensemble recruited during fear learning. Moreover, these results establish a model of fear memory formation in which intrinsic excitability determines neuronal selection, whereas learning-related encoding is governed by synaptic plasticity.
| Original language | Undefined/Unknown |
|---|---|
| Pages (from-to) | 364-375 |
| Number of pages | 12 |
| Journal | Molecular Psychiatry |
| Volume | 21 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 2016 |
Research programs
- EMC ONWAR-01-58-02
- EMC ONWAR-01-94-01