Bi-directional regulation of cognitive control by distinct prefrontal cortical output neurons to thalamus and striatum

The medial prefrontal cortex (mPFC) steers goal-directed actions and withholds inappropriate behavior. Dorsal and ventral mPFC (dmPFC/vmPFC) circuits have distinct roles in cognitive control, but underlying mechanisms are poorly understood. Here we use neuroanatomical tracing techniques, in vitro electrophysiology, chemogenetics and fiber photometry in rats engaged in a 5-choice serial reaction time task to characterize dmPFC and vmPFC outputs to distinct thalamic and striatal subdomains. We identify four spatially segregated projection neuron populations in the mPFC. Using fiber photometry we show that these projections distinctly encode behavior. Postsynaptic striatal and thalamic neurons differentially process synaptic inputs from dmPFC and vmPFC, highlighting mechanisms that potentially amplify distinct pathways underlying cognitive control of behavior. Chemogenetic silencing of dmPFC and vmPFC projections to lateral and medial mediodorsal thalamus subregions oppositely regulate cognitive control. In addition, dmPFC neurons projecting to striatum and thalamus divergently regulate cognitive control. Collectively, we show that mPFC output pathways targeting anatomically and functionally distinct striatal and thalamic subregions encode bi-directional command of cognitive control. This study presents an anatomical, neurophysiological and functional characterization of four distinct prefrontal populations that project to striatal and thalamic sub-regions. The authors show that each of these populations have a discrete role in the regulation of cognitive control.

Automated summary

The study identifies four distinct populations of prefrontal neurons projecting to different sub-regions of the striatum and thalamus, each playing a discrete role in the regulation of cognitive control. Dorsal and ventral mPFC circuits exhibit differential synaptic inputs to postsynaptic striatal and thalamic neurons, potentially amplifying distinct pathways underlying cognitive control. Chemogenetic silencing of specific mPFC projections to thalamic subregions oppositely regulate cognitive control, highlighting the complex mechanisms involved in behavior regulation.