Author:
Tsai Yuan-Chen,Hleihil Mohammad,Otomo Kanako,Abegg Andrin,Cavaccini Anna,Panzanelli Patrizia,Cramer Teresa,Ferrari Kim David,Barrett Matthew J. P.,Bosshard Giovanna,Karayannis Theofanis,Weber Bruno,Tyagarajan Shiva K.,Stobart Jillian L.
Abstract
AbstractGephyrin is the main scaffolding protein at inhibitory postsynaptic sites, and its clusters are the signaling hubs where several molecular pathways converge. Post-translational modifications (PTMs) of gephyrin alter GABAA receptor clustering at the synapse, but it is unclear how this affects neuronal activity at the circuit level. We assessed the contribution of gephyrin PTMs to microcircuit activity in the mouse barrel cortex by slice electrophysiology and in vivo two-photon calcium imaging of layer 2/3 (L2/3) pyramidal cells during single-whisker stimulation. Our results suggest that, depending on the type of gephyrin PTM, the neuronal activities of L2/3 pyramidal neurons can be differentially modulated, leading to changes in the size of the neuronal population responding to the single-whisker stimulation. Furthermore, we show that gephyrin PTMs have their preference for selecting synaptic GABAA receptor subunits. Our results identify an important role of gephyrin and GABAergic postsynaptic sites for cortical microcircuit function during sensory stimulation.
Funder
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Olga Mayenfisch Stiftung
Natural Sciences and Engineering Research Council of Canada
Publisher
Springer Science and Business Media LLC
Cited by
3 articles.
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