Beyond the Relay: Mediodorsal Thalamic Regulation of Prefrontal Cortex in Cue Detection
| dc.contributor.author | Runyon, Kelly Elizabeth | en |
| dc.contributor.committeechair | Howe, William Matthew | en |
| dc.contributor.committeemember | Clinton, Sarah | en |
| dc.contributor.committeemember | Farris, Shannon Lynn | en |
| dc.contributor.committeemember | Hodes, Georgia E. | en |
| dc.contributor.committeemember | Swanger, Sharon Ann | en |
| dc.contributor.department | Neuroscience | en |
| dc.date.accessioned | 2026-06-17T08:00:52Z | en |
| dc.date.available | 2026-06-17T08:00:52Z | en |
| dc.date.issued | 2026-06-16 | en |
| dc.description.abstract | The mediodorsal thalamus (MD) is a critical node within thalamocortical networks supporting prefrontal-dependent cognition, yet whether its projections to distinct prefrontal subregions constitute functionally specialized pathways has not been directly examined. Here we combined retrograde anatomical circuit mapping with projection-specific fiber photometry to characterize the structural and functional organization of MD connectivity with the prelimbic cortex (PRL), anterior cingulate cortex (ACC), and orbitofrontal cortex (OFC) in mice. Retrograde tracing revealed that MD neurons projecting to PRL and ACC originate from anatomically segregated subpopulations within the lateral MD subdivision (MDL), organized along its anterior-posterior axis and forming distinct reciprocal loops with each cortical target. Projection-specific calcium imaging during Pavlovian cue-reward conditioning revealed divergent dynamics across pathways: MD-ACC terminals underwent pronounced learning-dependent temporal sharpening, with response precision increasing across acquisition and trial-by-trial dynamics becoming coupled to behavioral performance, while MD-PRL terminals showed stable, sustained cue-evoked responses that did not reshape across learning. MD-OFC terminals showed no learning-related changes during Pavlovian conditioning, consistent with OFC's established role in action-outcome rather than cue-association learning, motivating a targeted examination of MD-OFC dynamics during an instrumental task, in which the animal must explicitly use the cue to guide behavior. During instrumental performance, MD-OFC terminals exhibited robust trial-phase-specific modulation that was absent during Pavlovian conditioning, including history-dependent pre-trial baseline signals that predicted upcoming behavioral performance, post-outcome signals encoding reward identity, and across-trial carryover effects linking outcome experience to future circuit state. Together, these findings demonstrate that MD is a functionally heterogeneous nucleus whose anatomically segregated projections support complementary aspects of cue-guided learning and flexible behavior, positioning MD as an active regulator of prefrontal computation rather than a passive thalamocortical relay. | en |
| dc.description.abstractgeneral | The brain's ability to use external cues to guide future decisions depends on communication between a structure deep in the brain called the thalamus and the prefrontal cortex, the region responsible for planning, decision making, and behavioral flexibility. A specific part of the thalamus called the mediodorsal nucleus sends connections to multiple regions of the prefrontal cortex, but it has long been unclear whether these connections all do the same thing or whether different connections serve different purposes. In this dissertation, we addressed this question in mice by first mapping the anatomy of these connections and then recording the activity of specific thalamic pathways while mice learned to respond to visual cues for reward. We found that connections from the mediodorsal thalamus to different prefrontal regions are physically separated within the thalamus and carry distinct signals during behavior. One pathway, connecting to a region called the anterior cingulate cortex, became more closely linked to the animal's behavioral performance as learning progressed. A second pathway, connecting to the prelimbic cortex, remained stable across learning, consistent with a role in maintaining learned associations rather than updating them. A third pathway, connecting to the orbitofrontal cortex, was uniquely activated during tasks that required animals to act on cues and evaluate the consequences of their actions, carrying signals that reflected recent outcome history and predicted how well the animal would perform on the next trial. Together, these findings reveal that the mediodorsal thalamus is not a single uniform relay but a collection of specialized pathways that each contribute differently to flexible, experience-guided behavior. This work has implications for understanding psychiatric conditions such as schizophrenia, in which thalamocortical communication is disrupted, and suggests that different aspects of cognitive dysfunction in these disorders may reflect damage to specific thalamic pathways rather than a general breakdown in thalamocortical communication. | en |
| dc.description.degree | Doctor of Philosophy | en |
| dc.format.medium | ETD | en |
| dc.identifier.other | vt_gsexam:46911 | en |
| dc.identifier.uri | https://hdl.handle.net/10919/143436 | en |
| dc.language.iso | en | en |
| dc.publisher | Virginia Tech | en |
| dc.rights | Creative Commons Attribution-NonCommercial 4.0 International | en |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc/4.0/ | en |
| dc.subject | mediodorsal thalamus | en |
| dc.subject | prelimbic cortex | en |
| dc.subject | anterior cingulate cortex | en |
| dc.subject | orbitofrontal cortex | en |
| dc.subject | cue detection | en |
| dc.subject | fiber photometry | en |
| dc.subject | attention | en |
| dc.subject | neuropsychiatric disease | en |
| dc.subject | thalamocortical circuitry | en |
| dc.subject | thalamus projection anatomy | en |
| dc.title | Beyond the Relay: Mediodorsal Thalamic Regulation of Prefrontal Cortex in Cue Detection | en |
| dc.type | Dissertation | en |
| thesis.degree.discipline | Neuroscience | en |
| thesis.degree.grantor | Virginia Polytechnic Institute and State University | en |
| thesis.degree.level | doctoral | en |
| thesis.degree.name | Doctor of Philosophy | en |
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