Anatomical and electrophysiological analysis of the fasciola cinerea of the mouse hippocampus.
Ioannis S ZouridisGiuseppe BalsamoPatricia Preston-FerrerAndrea BurgalossiPublished in: Hippocampus (2024)
The hippocampus is considered essential for several forms of declarative memory, including spatial and social memory. Despite the extensive research of the classic subfields of the hippocampus, the fasciola cinerea (FC)-a medially located structure within the hippocampal formation-has remained largely unexplored. In the present study, we performed a morpho-functional characterization of principal neurons in the mouse FC. Using in vivo juxtacellular recording of single neurons, we found that FC neurons are distinct from neighboring CA1 pyramidal cells, both morphologically and electrophysiologically. Specifically, FC neurons displayed non-pyramidal morphology and granule cell-like apical dendrites. Compared to neighboring CA1 pyramidal neurons, FC neurons exhibited more regular in vivo firing patterns and a lower tendency to fire spikes at short interspike intervals. Furthermore, tracing experiments revealed that the FC receives inputs from the lateral but not the medial entorhinal cortex and CA3, and it provides a major intra-hippocampal projection to the septal CA2 and sparser inputs to the distal CA1. Overall, our results indicate that the FC is a morphologically and electrophysiologically distinct subfield of the hippocampal formation; given the established role of CA2 in social memory and seizure initiation, the unique efferent intra-hippocampal connectivity of the FC points to possible roles in social cognition and temporal lobe epilepsy.
Keyphrases
- temporal lobe epilepsy
- spinal cord
- cerebral ischemia
- healthcare
- working memory
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- minimally invasive
- stem cells
- cognitive impairment
- subarachnoid hemorrhage
- white matter
- computed tomography
- multiple sclerosis
- functional connectivity
- magnetic resonance
- bone marrow
- blood brain barrier
- cell therapy
- prefrontal cortex
- mesenchymal stem cells
- cell death
- atrial fibrillation
- brain injury