Association cortical areas in the mouse contain a large population of fast‐spiking GABAergic neurons that do not express parvalbumin

Author:

Courcelles Erik Justin1,Kjelsberg Kasper1,Convertino Laura1,Nair Rajeevkumar Raveendran1,Witter Menno P.1,Nigro Maximiliano José1

Affiliation:

1. Kavli Institute for Systems Neuroscience, Center for Algorithms in the Cortex, Egil and Pauline Braathen and Fred Kavli Center for Cortical Microcircuits Norwegian University of Science and Technology Trondheim Norway

Abstract

AbstractGABAergic neurons represent 10–15% of the neuronal population of the cortex but exert a powerful control over information flow in cortical circuits. The largest GABAergic class in the neocortex is represented by the parvalbumin‐expressing fast‐spiking neurons, which provide powerful somatic inhibition to their postsynaptic targets. Recently, the density of parvalbumin interneurons has been shown to be lower in associative areas of the mouse cortex as compared with sensory and motor areas. Modelling work based on these quantifications linked the low‐density of parvalbumin interneurons with specific computations of associative cortices. However, it is still unknown whether the total GABAergic population of association cortices is smaller or whether another GABAergic type can compensate for the low density of parvalbumin interneurons. In the present study, we investigated these hypotheses using a combination of neuroanatomy, mouse genetics and neurophysiology. We found that the GABAergic population of association areas is comparable with that of primary sensory areas, and it is enriched of fast‐spiking neurons that do not express parvalbumin and were not accounted for by previous quantifications. We developed an intersectional viral strategy to demonstrate that the population of fast‐spiking neurons is comparable across cortical regions. Our results provide quantifications of the density of fast‐spiking GABAergic neurons and offers new biological constrains to refine current models of cortical computations.

Funder

Norges Forskningsråd

Kavli Foundation

Publisher

Wiley

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