Synaptic plasticity-dependent competition rule influences memory formation

Memory is supported by a specific collection of neurons distributed in broad brain areas, an engram. Despite recent advances in identifying an engram, how the engram is created during memory formation remains elusive. To explore the relation between a specific pattern of input activity and memory allocation, here we target a sparse subset of neurons in the auditory cortex and thalamus. The synaptic inputs from these neurons to the lateral amygdala (LA) are not potentiated by fear conditioning. Using an optogenetic priming stimulus, we manipulate these synapses to be potentiated by the learning. In this condition, fear memory is preferentially encoded in the manipulated cell ensembles. This change, however, is abolished with optical long-term depression (LTD) delivered shortly after training. Conversely, delivering optical long-term potentiation (LTP) alone shortly after fear conditioning is sufficient to induce the preferential memory encoding. These results suggest a synaptic plasticity-dependent competition rule underlying memory formation. Cellular activity level at the time of learning is thought to be a critical factor to determine which neurons are recruited to encode memory. Here, the authors show that competitive synaptic plasticity mechanisms influence which neurons will encode a fear memory.

Automated summary

The study investigates how synaptic plasticity of neurons influences the encoding of fear memories, showing that this process can be manipulated through optogenetic techniques. The encoding of memory is influenced by the competitive interactions of cellular activity levels and synaptic plasticity.