Degraded tactile coding in the Cntnap2 mouse model of autism

Atypical sensory processing is common in autism, but how neural coding is disrupted in sensory cortex is unclear. We evaluate whisker touch coding in L2/3 of somatosensory cortex (S1) in Cntnap2<sup>-/-</sup> mice, which have reduced inhibition. This classically predicts excess pyramidal cell spiking, but this remains controversial, and other deficits may dominate. We find that c-fos expression is elevated in S1 of Cntnap2<sup>-/-</sup> mice under spontaneous activity conditions but is comparable to that of control mice after whisker stimulation, suggesting normal sensory-evoked spike rates. GCaMP8m imaging from L2/3 pyramidal cells shows no excess whisker responsiveness, but it does show multiple signs of degraded somatotopic coding. This includes broadened whisker-tuning curves, a blurred whisker map, and blunted whisker point representations. These disruptions are greater in noisy than in sparse sensory conditions. Tuning instability across days is also substantially elevated in Cntnap2<sup>-/-</sup>. Thus, Cntnap2<sup>-/-</sup> mice show no excess sensory-evoked activity, but a degraded and unstable tactile code in S1.

Authors

Institutions

Publication Details

Journal
Cell Reports
Published
2024-08-01
DOI
https://doi.org/10.1016/j.celrep.2024.114612
Citations
8
Primary Topic
Neuroscience and Neural Engineering
Type
article
Field-Weighted Citation Impact
2.15

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Degraded tactile coding in the Cntnap2 mouse model of autism

Han Chin Wang, Daniel E. Feldman
8 citations
Cell Reports
Neuroscience and Neural Engineering
2.15
article

Degraded tactile coding in the Cntnap2 mouse model of autism

Han Chin Wang, Daniel E. Feldman
article en
8 citations

Abstract

Atypical sensory processing is common in autism, but how neural coding is disrupted in sensory cortex is unclear. We evaluate whisker touch coding in L2/3 of somatosensory cortex (S1) in Cntnap2<sup>-/-</sup> mice, which have reduced inhibition. This classically predicts excess pyramidal cell spiking, but this remains controversial, and other deficits may dominate. We find that c-fos expression is elevated in S1 of Cntnap2<sup>-/-</sup> mice under spontaneous activity conditions but is comparable to that of control mice after whisker stimulation, suggesting normal sensory-evoked spike rates. GCaMP8m imaging from L2/3 pyramidal cells shows no excess whisker responsiveness, but it does show multiple signs of degraded somatotopic coding. This includes broadened whisker-tuning curves, a blurred whisker map, and blunted whisker point representations. These disruptions are greater in noisy than in sparse sensory conditions. Tuning instability across days is also substantially elevated in Cntnap2<sup>-/-</sup>. Thus, Cntnap2<sup>-/-</sup> mice show no excess sensory-evoked activity, but a degraded and unstable tactile code in S1.

Cell ReportsVol. 43(8)
University of California, Berkeley (US)
Simons Foundation Autism Research Initiative, National Institutes of Health
Openalex Percentile: Top 13%
Neuroscience and Neural Engineering
2.15
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.