AI Article Synopsis

  • Immediate-early genes (IEGs), like c-fos, are used to identify active neural groups related to specific memories or behaviors, mainly in complex brain areas like the hippocampus and prefrontal cortex.
  • This study investigates IEG expression in the primary somatosensory cortex (S1) during a learning task related to whisker responses and finds that training does not change IEG expression in the superficial layers of S1.
  • Despite training enhancing overall synaptic strength in neurons, the study reveals that the synaptic strengthening occurs mainly in neurons that do not express the fosGFP reporter, suggesting that traditional IEG measures may not effectively identify learning-specific memories in S1.

Article Abstract

Immediate-early gene (IEG) expression has been used to identify small neural ensembles linked to a particular experience, based on the principle that a selective subset of activated neurons will encode specific memories or behavioral responses. The majority of these studies have focused on "engrams" in higher-order brain areas where more abstract or convergent sensory information is represented, such as the hippocampus, prefrontal cortex, or amygdala. In primary sensory cortex, IEG expression can label neurons that are responsive to specific sensory stimuli, but experience-dependent shaping of neural ensembles marked by IEG expression has not been demonstrated. Here, we use a fosGFP transgenic mouse to longitudinally monitor in vivo expression of the activity-dependent gene c-fos in superficial layers (L2/3) of primary somatosensory cortex (S1) during a whisker-dependent learning task. We find that sensory association training does not detectably alter fosGFP expression in L2/3 neurons. Although training broadly enhances thalamocortical synaptic strength in pyramidal neurons, we find that synapses onto fosGFP+ neurons are not selectively increased by training; rather, synaptic strengthening is concentrated in fosGFP- neurons. Taken together, these data indicate that expression of the IEG reporter fosGFP does not facilitate identification of a learning-specific engram in L2/3 in barrel cortex during whisker-dependent sensory association learning.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8719899PMC
http://dx.doi.org/10.1073/pnas.2112212118DOI Listing

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