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An identified ensemble within a neocortical circuit encodes essential information for genetically-enhanced visual shape learning.

Hippocampus | 2019

Advanced cognitive tasks are encoded in distributed neocortical circuits that span multiple forebrain areas. Nonetheless, synaptic plasticity and neural network theories hypothesize that essential information for performing these tasks is encoded in specific ensembles within these circuits. Relatively simpler subcortical areas contain specific ensembles that encode learning, suggesting that neocortical circuits contain such ensembles. Previously, using localized gene transfer of a constitutively active protein kinase C (PKC), we established that a genetically-modified circuit in rat postrhinal cortex, part of the hippocampal formation, can encode some essential information for performing specific visual shape discriminations. However, these studies did not identify any specific neurons that encode learning; the entire circuit might be required. Here, we show that both learning and recall require fast neurotransmitter release from an identified ensemble within this circuit, the transduced neurons; we blocked fast release from these neurons by coexpressing a Synaptotagmin I siRNA with the constitutively active PKC. During learning or recall, specific signaling pathways required for learning are activated in this ensemble; during learning, calcium/calmodulin-dependent protein kinase II, MAP kinase, and CREB are activated; and, during recall, dendritic protein synthesis and CREB are activated. Using activity-dependent gene imaging, we showed that during learning, activity in this ensemble is required to recruit and activate the circuit. Further, after learning, during image presentation, blocking activity in this ensemble reduces accuracy, even though most of the rest of the circuit is activated. Thus, an identified ensemble within a neocortical circuit encodes essential information for performing an advanced cognitive task.

Pubmed ID: 30734387 RIS Download

Associated grants

  • Agency: NINDS NIH HHS, United States
    Id: NS045855
  • Agency: NINDS NIH HHS, United States
    Id: NS057558
  • Agency: NINDS NIH HHS, United States
    Id: NS086960
  • Agency: NIH HHS, United States
    Id: AG025894
  • Agency: NIH HHS, United States
    Id: NS057558
  • Agency: NIH HHS, United States
    Id: NS045855
  • Agency: NIH HHS, United States
    Id: NS086960
  • Agency: NIH HHS, United States
    Id: AG025894
  • Agency: National Science Foundation (NSF), International

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