Specialized coding patterns among dorsomedial prefrontal neuronal ensembles predict conditioned reward seeking.
Roger I GrantElizabeth M DoncheckKelsey M VollmerKion T WinstonElizaveta V RomanovaPreston N SieglerHeather HolmanChristopher W BowenJames M OtisPublished in: eLife (2021)
Non-overlapping cell populations within dorsomedial prefrontal cortex (dmPFC), defined by gene expression or projection target, control dissociable aspects of reward seeking through unique activity patterns. However, even within these defined cell populations, considerable cell-to-cell variability is found, suggesting that greater resolution is needed to understand information processing in dmPFC. Here, we use two-photon calcium imaging in awake, behaving mice to monitor the activity of dmPFC excitatory neurons throughout Pavlovian reward conditioning. We characterize five unique neuronal ensembles that each encodes specialized information related to a sucrose reward, reward-predictive cues, and behavioral responses to those cues. The ensembles differentially emerge across daily training sessions - and stabilize after learning - in a manner that improves the predictive validity of dmPFC activity dynamics for deciphering variables related to behavioral conditioning. Our results characterize the complex dmPFC neuronal ensemble dynamics that stably predict reward availability and initiation of conditioned reward seeking following cue-reward learning.
Keyphrases
- prefrontal cortex
- gene expression
- single cell
- cell therapy
- mental health
- stem cells
- dna methylation
- mass spectrometry
- high resolution
- healthcare
- spinal cord
- type diabetes
- adipose tissue
- magnetic resonance imaging
- computed tomography
- magnetic resonance
- metabolic syndrome
- single molecule
- high frequency
- social media
- convolutional neural network
- fluorescent probe
- deep learning
- deep brain stimulation
- drug induced
- genetic diversity