Sensory representation of an auditory cued tactile stimulus in the posterior parietal cortex of the mouse

Hemanth Mohan, Yasir Gallero-Salas, Stefano Carta, João Sacramento, Balazs Laurenczy, Lazar T. Sumanovski, Christiaan P.J. De Kock, Fritjof Helmchen, Shankar Sachidhanandam*

*Corresponding author for this work

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Sensory association cortices receive diverse inputs with their role in representing and integrating multi-sensory content remaining unclear. Here we examined the neuronal correlates of an auditory-tactile stimulus sequence in the posterior parietal cortex (PPC) using 2-photon calcium imaging in awake mice. We find that neuronal subpopulations in layer 2/3 of PPC reliably represent texture-touch events, in addition to auditory cues that presage the incoming tactile stimulus. Notably, altering the flow of sensory events through omission of the cued texture touch elicited large responses in a subset of neurons hardly responsive to or even inhibited by the tactile stimuli. Hence, PPC neurons were able to discriminate not only tactile stimulus features (i.e., texture graininess) but also between the presence and omission of the texture stimulus. Whereas some of the neurons responsive to texture omission were driven by looming-like auditory sounds others became recruited only with tactile sensory experience. These findings indicate that layer 2/3 neuronal populations in PPC potentially encode correlates of expectancy in addition to auditory and tactile stimuli.

Original languageEnglish
Article number7739
JournalScientific Reports
Volume8
Issue number1
DOIs
Publication statusPublished - 17 May 2018

Funding

We thank A. Gilad for help with analysis. We thank R. Hahnloser and D. Rodrigues for help with the sound recordings. We thank S. Ciocchi, M. Acuna and F. Kasanetz for useful comments on earlier versions of the manuscript. This work was supported by the Swiss National Science Foundation (SNSF; grant 31003A_149858 to F.H.) and the University of Bern. H.M. was supported by the Boehringer Ingelheim Travel Grant and by an Erasmus Mundus Joint Doctorate grant (ENCNetwork c3-p3).

FundersFunder number
Boehringer IngelheimENCNetwork c3-p3
Universität Bern
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung31003A_149858

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