| Literature DB >> 33529646 |
Barna Dudok1, Peter M Klein2, Ernie Hwaun2, Brian R Lee3, Zizhen Yao3, Olivia Fong3, John C Bowler4, Satoshi Terada4, Fraser T Sparks4, Gergely G Szabo2, Jordan S Farrell2, Jim Berg3, Tanya L Daigle3, Bosiljka Tasic3, Jordane Dimidschstein5, Gord Fishell6, Attila Losonczy7, Hongkui Zeng3, Ivan Soltesz2.
Abstract
Interneurons expressing cholecystokinin (CCK) and parvalbumin (PV) constitute two key GABAergic controllers of hippocampal pyramidal cell output. Although the temporally precise and millisecond-scale inhibitory regulation of neuronal ensembles delivered by PV interneurons is well established, the in vivo recruitment patterns of CCK-expressing basket cell (BC) populations has remained unknown. We show in the CA1 of the mouse hippocampus that the activity of CCK BCs inversely scales with both PV and pyramidal cell activity at the behaviorally relevant timescales of seconds. Intervention experiments indicated that the inverse coupling of CCK and PV GABAergic systems arises through a mechanism involving powerful inhibitory control of CCK BCs by PV cells. The tightly coupled complementarity of two key microcircuit regulatory modules demonstrates a novel form of brain-state-specific segregation of inhibition during spontaneous behavior.Entities:
Keywords: CA1; CB1 receptor; GABA; Sncg; brain state; cholecystokinin; hippocampus; inhibition; interneuron; locomotion; parvalbumin
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Year: 2021 PMID: 33529646 PMCID: PMC7979482 DOI: 10.1016/j.neuron.2021.01.003
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173