Abstract

Anatomical and physiological studies have described the cortex as a six-layer structure that receives, elaborates, and sends out information exclusively as excitatory output to cortical and subcortical regions. This concept has increasingly been challenged by several anatomical and functional studies that showed that direct inhibitory cortical outputs are also a common feature of the sensory and motor cortices. Similar to their excitatory counterparts, subsets of Somatostatin- and Parvalbumin-expressing neurons have been shown to innervate distal targets like the sensory and motor striatum and the contralateral cortex. However, no evidence of long-range VIP-expressing neurons, the third major class of GABAergic cortical inhibitory neurons, has been shown in such cortical regions. Here, using anatomical anterograde and retrograde viral tracing, we tested the hypothesis that VIP-expressing neurons of the mouse auditory and motor cortices can also send long-range projections to cortical and subcortical areas. We were able to demonstrate, for the first time, that VIP-expressing neurons of the auditory cortex can reach not only the contralateral auditory cortex and the ipsilateral striatum and amygdala, as shown for Somatostatin- and Parvalbumin-expressing long-range neurons, but also the medial geniculate body and both superior and inferior colliculus. We also demonstrate that VIP-expressing neurons of the motor cortex send long-range GABAergic projections to the dorsal striatum and contralateral cortex. Because of its presence in two such disparate cortical areas, this would suggest that the long-range VIP projection is likely a general feature of the cortex’s network.

Highlights

  • The auditory cortex is a six-layer structure characterized by different cell types

  • In a very simplistic way, these neurons, according to the neurotransmitter they release, can be divide into two main groups: glutamatergic/excitatory pyramidal neurons and GABAergic/inhibitory neurons. This neuronal subdivision of the cortex leads to the Abbreviations: AC, auditory cortex; ACA, anterior cingulate cortex; ACB, nucleus accumbens; CA1, Cornu Ammonis of the hippocampus subfield 1; CA3, Cornu Ammonis of the hippocampus subfield 3; cc, corpus callosum; CP, caudoputamen; DG, dentate gyrus; ENT, enthorinal cortex; HPF, hippocampal formation; HY, hypothalamus; IC, inferior colliculus; ICe, inferior colliculus, external; LA, lateral amygdala; LGN, lateral geniculate nucleus; LS, lateral septal nucleus; MB, midbrain; MC, motor cortex; MGB, medial geniculate body; MS, medial septal nucleus; NB, nucleus of the brachium of the inferior colliculus; PAG, periacqueductal grey; PG, pontine gray; PIR, piriform cortex; RSP, retrosplenial cortex; SC, superior colliculus; SN, substantia nigra; SS, somatosensory cortex; STR, striatum; TeA, temporal association cortex; TH, thalamus; VIS, visual cortex; VTA, ventrotegmental area

  • A central question of modern neuroscience is determining the whole connectome of the mammalian brain (Abbott et al, 2020) and how many different cell types contribute to signal processing within specific neuronal networks to control behavior

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Summary

Introduction

The auditory cortex is a six-layer structure characterized by different cell types. In a very simplistic way, these neurons, according to the neurotransmitter they release, can be divide into two main groups: glutamatergic/excitatory pyramidal neurons (about 70–80%) and GABAergic/inhibitory neurons (about 20–30%). No long-range GABAergic VIP-expressing neurons from these cortical regions have been shown yet We addressed this fundamental question using anterograde and retrograde anatomical methods. Using these techniques, we demonstrate, for the first time, the existence of VIP-expressing GABAergic neurons in the auditory and motor cortices with cortico-cortical and cortico-subcortical long-range GABAergic projections

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