Pathway-, layer- and cell-type-specific thalamic input to mouse barrel cortex
B Semihcan Sermet,
Pavel Truschow,
Michael Feyerabend,
Johannes M Mayrhofer,
Tess B Oram,
Ofer Yizhar,
Jochen F Staiger,
Carl CH Petersen
Affiliations
B Semihcan Sermet
Laboratory of Sensory Processing, Brain Mind Institute, Faculty of Life Sciences, Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland
Pavel Truschow
Institute for Neuroanatomy,University Medical Center, Georg-August-University Goettingen, Goettingen, Germany
Michael Feyerabend
Institute for Neuroanatomy,University Medical Center, Georg-August-University Goettingen, Goettingen, Germany
Johannes M Mayrhofer
Laboratory of Sensory Processing, Brain Mind Institute, Faculty of Life Sciences, Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland
Tess B Oram
Department of Neurobiology, Weizmann Institute of Science, Rehovot, Israel
Laboratory of Sensory Processing, Brain Mind Institute, Faculty of Life Sciences, Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland
Mouse primary somatosensory barrel cortex (wS1) processes whisker sensory information, receiving input from two distinct thalamic nuclei. The first-order ventral posterior medial (VPM) somatosensory thalamic nucleus most densely innervates layer 4 (L4) barrels, whereas the higher-order posterior thalamic nucleus (medial part, POm) most densely innervates L1 and L5A. We optogenetically stimulated VPM or POm axons, and recorded evoked excitatory postsynaptic potentials (EPSPs) in different cell-types across cortical layers in wS1. We found that excitatory neurons and parvalbumin-expressing inhibitory neurons received the largest EPSPs, dominated by VPM input to L4 and POm input to L5A. In contrast, somatostatin-expressing inhibitory neurons received very little input from either pathway in any layer. Vasoactive intestinal peptide-expressing inhibitory neurons received an intermediate level of excitatory input with less apparent layer-specificity. Our data help understand how wS1 neocortical microcircuits might process and integrate sensory and higher-order inputs.