Abstract
The prefrontal cortex (PFC) and hippocampus (HPC) reportedly play crucial roles in the flexible use of stored information according to context. However, it remains unclear whether and how their neural representations differ during the context-guided retrieval. To solve this problem, we examined neural activity in the lateral PFC (lPFC, 470 neurons), medial PFC (mPFC, 322 neurons), and HPC (456 neurons) of three male macaques performing an item-location association memory task. The task required the animals to remember the location of a firstly presented item-cue relative to a background image that was later shown with a tilt as a context-cue. Population decoding analyses using all recorded neurons suggested that the lPFC and HPC (but not the mPFC) represented substantial task-related information. However, the represented contents differed between the two areas, both before and after the context-cue. Before the context-cue, the lPFC represented only the location retrieved from the item-cue, while the HPC also represented the item-cue itself. After the context-cue, the lPFC demonstrated a selective representation of the target-location regardless of the context-cue. In contrast, the HPC represented the three task-related pieces of information equivalently. These results suggest that the lPFC selectively represents goal-directed information at that moment among task-related information, while the HPC automatically represents a task event and its mnemonically linked information, implying complementary functional roles of the two brain regions as "regulator" and "supplier" in the context-guided memory process.