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Functional specialization of hippocampal somatostatin-expressing interneurons.


ABSTRACT: Hippocampal somatostatin-expressing (Sst) GABAergic interneurons (INs) exhibit considerable anatomical and functional heterogeneity. Recent single cell transcriptome analyses have provided a comprehensive Sst-IN subtype census, a plausible molecular ground truth of neuronal identity whose links to specific functionality remain incomplete. Here, we designed an approach to identify and access subpopulations of Sst-INs based on transcriptomic features. Four mouse models based on single or combinatorial Cre- and Flp- expression differentiated functionally distinct subpopulations of CA1 hippocampal Sst-INs that largely tiled the morpho-functional parameter space of the Sst-INs superfamily. Notably, the Sst;;Tac1 intersection revealed a population of bistratified INs that preferentially synapsed onto fast-spiking interneurons (FS-INs) and were both necessary and sufficient to interrupt their firing. In contrast, the Ndnf;;Nkx2-1 intersection identified a population of oriens lacunosum-moleculare (OLM) INs that predominantly targeted CA1 pyramidal neurons, avoiding FS-INs. Overall, our results provide a framework to translate neuronal transcriptomic identity into discrete functional subtypes that capture the diverse specializations of hippocampal Sst-INs.

SUBMITTER: Chamberland S 

PROVIDER: S-EPMC10168348 | biostudies-literature | 2023 Apr

REPOSITORIES: biostudies-literature

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Functional specialization of hippocampal somatostatin-expressing interneurons.

Chamberland Simon S   Grant Gariel G   Machold Robert R   Nebet Erica R ER   Tian Guoling G   Hanani Monica M   Kullander Klas K   Tsien Richard W RW  

bioRxiv : the preprint server for biology 20230427


Hippocampal somatostatin-expressing (<i>Sst</i>) GABAergic interneurons (INs) exhibit considerable anatomical and functional heterogeneity. Recent single cell transcriptome analyses have provided a comprehensive <i>Sst</i>-IN subtype census, a plausible molecular ground truth of neuronal identity whose links to specific functionality remain incomplete. Here, we designed an approach to identify and access subpopulations of <i>Sst</i>-INs based on transcriptomic features. Four mouse models based o  ...[more]

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