Distinct developmental trajectories of externally- and internally-generated hippocampal sequences and assemblies
The hippocampus generates cognitive maps through two distinct mechanisms: external representations anchored to environmental landmarks and internal sequences integrating self-referenced information. In adult CA1, these functions segregate radially, with deep cells processing external cues and superficial cells handling internal representations. This anatomical organization suggests that developmental processes constrain the formation of these functionally distinct circuits. However, the developmental timeline for the emergence of these two types of hippocampal representations remains unknown. Using longitudinal two-photon calcium imaging in head-fixed mice during the third postnatal week, we investigated when internal versus external hippocampal representations emerge. We recorded from deep and superficial CA1 layers while mice ran on treadmills that are bare or enriched with tactile cues, addressing the challenge of tracking cells across sessions. Internal sequences emerge during the mid-fourth postnatal week, following the development of cue-based representations. These sequences initially encode elapsed time before evolving to integrate run distance, arising after rest cell assemblies as spatial coding and functional connectivity networks stabilize. These findings identify the mid fourth postnatal week as a critical developmental milestone marking the establishment of a balanced integration between external landmark-based and internal self-referenced spatial representations. This transition period may constitute a vulnerable developmental window during which disruptions could predispose to disorders characterised by altered cognitive maps. HighlightsO_LIP24 is critical for CA1 development C_LIO_LICue-based representations stabilize by P24 C_LIO_LIInternal sequences emerge at P24, encoding run duration before distance C_LIO_LICell assemblies form before internal sequences C_LI