Id2 GABAergic interneurons comprise a neglected fourth major group of cortical inhibitory cells

Cortical GABAergic interneurons (INs) represent a diverse population of mainly locally projecting cells that provide specialized forms of inhibition to pyramidal neurons and other INs. Most recent work on INs has focused on subtypes distinguished by expression of Parvalbumin (PV), Somatostatin (SST)...

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Detalles Bibliográficos
Autores: Machold, Robert, Dellal, Shlomo, Valero, Manuel, Zurita, Hector, Kruglikov, Ilya, Meng, John Hongyu, Hanson, Jessica L., Hashikawa, Yoshiko, Schuman, Benjamin, Buzsáki, György, Rudy, Bernardo
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2023
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:10230/60069
Acceso en línea:http://hdl.handle.net/10230/60069
http://dx.doi.org/10.7554/eLife.85893
Access Level:acceso abierto
Palabra clave:GABAergic Interneurons
Id2
Cortical inhibition
In vivo recordings
Intersectional genetics
Mouse
Neurogliaform cells
Neuroscience
Descripción
Sumario:Cortical GABAergic interneurons (INs) represent a diverse population of mainly locally projecting cells that provide specialized forms of inhibition to pyramidal neurons and other INs. Most recent work on INs has focused on subtypes distinguished by expression of Parvalbumin (PV), Somatostatin (SST), or Vasoactive Intestinal Peptide (VIP). However, a fourth group that includes neurogliaform cells (NGFCs) has been less well characterized due to a lack of genetic tools. Here, we show that these INs can be accessed experimentally using intersectional genetics with the gene Id2. We find that outside of layer 1 (L1), the majority of Id2 INs are NGFCs that express high levels of neuropeptide Y (NPY) and exhibit a late-spiking firing pattern, with extensive local connectivity. While much sparser, non-NGFC Id2 INs had more variable properties, with most cells corresponding to a diverse group of INs that strongly expresses the neuropeptide CCK. In vivo, using silicon probe recordings, we observed several distinguishing aspects of NGFC activity, including a strong rebound in activity immediately following the cortical down state during NREM sleep. Our study provides insights into IN diversity and NGFC distribution and properties, and outlines an intersectional genetics approach for further study of this underappreciated group of INs.