Infrabarrels Are Layer 6 Circuit Modules in the Barrel Cortex that Link Long-Range Inputs and Outputs.

Cell Rep

Department of Neuroscience, Division of Biology and Medicine, Brown University, Providence, RI 02912, USA.

Published: December 2017

AI Article Synopsis

  • The rodent somatosensory cortex contains barrel columns, which are clusters of neurons in layer 4 (L4) that extend throughout the cortical depth.
  • Using a specific mouse model, researchers identified infrabarrels in layer 6 (L6) that correspond to L4 barrels, revealing distinct clusters of corticothalamic (CT) and corticocortical (CC) neurons.
  • Optogenetic experiments demonstrated that while CC neurons receive strong input from thalamic sources, CT neurons are less excitable and receive weaker input, highlighting the distinct roles and connectivity of these neuron types in the cortical circuitry.

Article Abstract

The rodent somatosensory cortex includes well-defined examples of cortical columns-the barrel columns-that extend throughout the cortical depth and are defined by discrete clusters of neurons in layer 4 (L4) called barrels. Using the cell-type-specific Ntsr1-Cre mouse line, we found that L6 contains infrabarrels, readily identifiable units that align with the L4 barrels. Corticothalamic (CT) neurons and their local axons cluster within the infrabarrels, whereas corticocortical (CC) neurons are densest between infrabarrels. Optogenetic experiments showed that CC cells received robust input from somatosensory thalamic nuclei, whereas CT cells received much weaker thalamic inputs. We also found that CT neurons are intrinsically less excitable, revealing that both synaptic and intrinsic mechanisms contribute to the low firing rates of CT neurons often reported in vivo. In summary, infrabarrels are discrete cortical circuit modules containing two partially separated excitatory networks that link long-distance thalamic inputs with specific outputs.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736017PMC
http://dx.doi.org/10.1016/j.celrep.2017.11.049DOI Listing

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