Intrinsic Dendritic Integration Features of Prefrontal Layer 5 Pyramidal Cell Subclasses

The prefrontal cortex (PFC) is an associative center that integrates various inputs to support cognition. Layer 5 pyramidal cells are themselves associative centers, as their dendrites span all cortical layers and sample multiple input streams. Backpropagating action potentials (bAPs) are an important mechanism for integrating synaptic inputs arriving at distinct dendritic locations. bAPs originating in the axon initial segment can depolarize the apical dendrite, activate voltage-gated currents that underlie dendritic processing and synaptic plasticity, and influence the integration of synaptic inputs arriving onto apical dendrites. How effectively bAPs depolarize apical dendrites depends on the cell type, dendritic morphology, and the dendrite's passive and active properties. Here, we found that in a unique subclass of PFC Layer 5 pyramidal cell defined by D3 dopamine receptor (D3R) expression, dendritic calcium responses to bAP stimuli were far greater for a burst of APs than expected from a linear sum of single AP-evoked events in mice of either sex. D3R-expressing neurons electrophysiologically resemble intratelencephalic, D1R-expressing pyramidal neurons but morphologically resemble pyramidal tract, D2R-expressing pyramidal neurons. In both D1R- and D2R-expressing cells, burst-evoked dendritic calcium events largely reflected a linear sum of individual AP responses. In D1R neurons, this was partially due to large-/big-conductance calcium–activated potassium (BK) channels, while in D2R neurons, both BK and hyperpolarization-activated cyclic nucleotide–gated channels contributed. These data demonstrate that the intrinsic dendritic excitability of PFC Layer 5 pyramidal cells widely differs and suggest that nonlinear dendritic excitability in D3R-expressing neurons uniquely positions these cells within PFC circuits.

• Publication year

  2025

• Venue

  Journal of Neuroscience

• Publication date

  2025-10-15

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1523/JNEUROSCI.1080-25.2025PMID 41093758PMCID PMC12660168
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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