Experience-Dependent Plasticity of Thalamoprefrontal Circuitry Characterizes Learning Across Species
Learning is an adaptive process which is thought to require precise coordination among multiple brain regions over time. Thalamoprefrontal circuitry is central to multiple domains of cognitive control and executive function, yet its evolution during learning is not characterized. In this study, we explored thalamoprefrontal circuit signaling in mice and connectivity dynamics in humans over the course of learning a homologous psychomotor task. In mice, we targeted a genetically encoded Ca2+indicator to the mediodorsal-prefrontal (MdT-dmPFC) projection and used fiber photometry to record synaptic dorsomedial PFC (dmPFC) activity. As learning sessions progressed, all mice demonstrated a decrease in reaction time (RT) performance on successful trials (p<0.001). In concomitant synaptic MdT-dmPFC circuit activity across sessions, we observed a significant increase in activity during the anticipatory (p<0.01) and reward retrieval (p<0.01) periods, and a non-significant trend towards an increase in preparatory activity (p<0.15). However, following the learning period, during task re-exposure, we observed a significant shift in circuit activity, away from anticipatory (p<0.001) and towards the preparatory period (p<0.001) over the course of re-exposure sessions. Furthermore, we observed an emergence of a learner (decrease in RT) and a non-learner group (increase in RT) during the task re-exposure period. Over the course of a single analogous task session in humans, we also observed a learner and a non-learner group. When analyzing the thalamoprefrontal regional connectivity dynamics of early and late trials for learners, we observed a significant increase in low frequency and decrease in high frequency synchrony (connectivity tilt) in thalamoprefrontal pathways during preparatory and anticipatory periods. Interestingly, pairwise interactions specifically between the anterior corona radiata (ACR) and superior frontal gyrus (SFG), the human homolog to the genetically targeted MdT-dmPFC circuitry in mice, in fact demonstrated a robustly opposite connectivity tilt effect distinguishing learners from non-learners (Cohens d > 2). Overall, these findings may provide cross-species evidence of novel, conserved thalamoprefrontal circuit mechanisms of adaptive learning.