A developmental cell-type switch in cortical interneurons leads to a selective defect in cortical oscillations

Naoki Takada, Hyun Jae Pi, Vitor H. Sousa, Jack Waters, Gord Fishell, Adam Kepecs, Pavel Osten

Research output: Contribution to journalArticlepeer-review

Abstract

The cellular diversity of interneurons in the neocortex is thought to reflect subtype-specific roles of cortical inhibition. Here we ask whether perturbations to two subtypes -parvalbumin-positive (PV+) and somatostatin-positive (SST+) interneurons -can be compensated for with respect to their contributions to cortical development. We use a genetic cell fate switch to delete both PV+ and SST+ interneurons selectively in cortical layers 2-4 without numerically changing the total interneuron population. This manipulation is compensated for at the level of synaptic currents and receptive fields (RFs) in the somatosensory cortex. By contrast, we identify a deficit in inhibitory synchronization in vitro and a large reduction in cortical gamma oscillations in vivo. This reveals that, while the roles of inhibition in establishing cortical inhibitory/excitatory balance and RFs can be subserved by multiple interneuron subtypes, gamma oscillations depend on cellular properties that cannot be compensated for -likely, the fast signalling properties of PV+ interneurons. & copy; 2014 Macmillan Publishers Limited. All rights reserved.

Original languageEnglish (US)
Article number5333
JournalNature communications
Volume5
DOIs
StatePublished - 2014

ASJC Scopus subject areas

  • General Chemistry
  • General Biochemistry, Genetics and Molecular Biology
  • General Physics and Astronomy

Fingerprint

Dive into the research topics of 'A developmental cell-type switch in cortical interneurons leads to a selective defect in cortical oscillations'. Together they form a unique fingerprint.

Cite this