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CA1 pyramidal cell diversity is rooted in the time of neurogenesis.

ABSTRACT: Cellular diversity supports the computational capacity and flexibility of cortical circuits. Accordingly, principal neurons at the CA1 output node of the murine hippocampus are increasingly recognized as a heterogeneous population. Their genes, molecular content, intrinsic morpho-physiology, connectivity, and function seem to segregate along the main anatomical axes of the hippocampus. Since these axes reflect the temporal order of principal cell neurogenesis, we directly examined the relationship between birthdate and CA1 pyramidal neuron diversity, focusing on the ventral hippocampus. We used a genetic fate-mapping approach that allowed tagging three groups of age-matched principal neurons: pioneer, early-, and late-born. Using a combination of neuroanatomy, slice physiology, connectivity tracing, and cFos staining in mice, we show that birthdate is a strong predictor of CA1 principal cell diversity. We unravel a subpopulation of pioneer neurons recruited in familiar environments with remarkable positioning, morpho-physiological features, and connectivity. Therefore, despite the expected plasticity of hippocampal circuits, given their role in learning and memory, the diversity of their main components is also partly determined at the earliest steps of development.

SUBMITTER: Cavalieri D

PROVIDER: S-EPMC8660020 | biostudies-literature |

REPOSITORIES: biostudies-literature

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A Computational Model of the Cholinergic Modulation of CA1 Pyramidal Cell Activity.

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RNA-Seq from CA1 pyramidal neurons

Project description:RNA-Seq from CA1 pyramidal neurons purified by FACS from 4-week-old mice.

2020-01-07 | GSE135147 | GEO

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TRPM4 Expression During Postnatal Developmental of Mouse CA1 Pyramidal Neurons.

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