4.6 Article

Abnormal Whisker-Dependent Behaviors and Altered Cortico-Hippocampal Connectivity in Shank3b-/- Mice

Journal

CEREBRAL CORTEX
Volume 32, Issue 14, Pages 3042-3056

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cercor/bhab399

Keywords

autism; connectivity; hippocampus; mouse; somatosensory

Categories

Funding

  1. Strategic Project TRAIN-Trentino Autism Initiative from the University of Trento
  2. University of Trento
  3. Fondazione CARITRO (Trento, Italy)
  4. Umberto Veronesi Foundation (Milan, Italy)
  5. CIMeC/University of Trento
  6. Brain and Behavior Research Foundation (NARSAD Young Investigator Grant) [26617]
  7. University of Trento (Starting Grant for Young Researchers)
  8. Armenise Harvard Foundation (Career Development Award)
  9. Simons Foundation [SFARI 400101]
  10. Brain and Behavior Foundation (NARSAD-National Alliance for Research on Schizophrenia and Depression)
  11. European Research Council (ERC-DISCONN) [GA802371]
  12. NIH [1R21MH116473-01A1]
  13. Telethon Foundation [GGP19177]

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Abnormal tactile response is a common feature in Autism Spectrum Disorders (ASDs), and patients with Phelan-McDermid syndrome (PMS) also exhibit similar tactile response abnormalities. This study investigated the neural substrates involved in whisker-guided behaviors in Shank3b(-/-) mice, which showed deficits in texture discrimination and low responsiveness to repetitive whisker stimulation. Reduced activation in the primary somatosensory cortex (S1) and hippocampus was observed, suggesting impaired sensory processing. Resting-state fMRI further revealed decreased connectivity between S1 and the hippocampus, potentially impairing whisker-dependent cues recognition.
Abnormal tactile response is an integral feature of Autism Spectrum Disorders (ASDs), and hypo-responsiveness to tactile stimuli is often associated with the severity of ASDs core symptoms. Patients with Phelan-McDermid syndrome (PMS), caused by mutations in the SHANK3 gene, show ASD-like symptoms associated with aberrant tactile responses. The neural underpinnings of these abnormalities are still poorly understood. Here we investigated, in Shank3b(-/-) adult mice, the neural substrates of whisker-guided behaviors, a key component of rodents' interaction with the surrounding environment. We assessed whisker-dependent behaviors in Shank3b(-/-) adult mice and age-matched controls, using the textured novel object recognition (tNORT) and whisker nuisance (WN) test. Shank3b(-/-) mice showed deficits in whisker-dependent texture discrimination in tNORT and behavioral hypo-responsiveness to repetitive whisker stimulation in WN. Sensory hypo-responsiveness was accompanied by a significantly reduced activation of the primary somatosensory cortex (S1) and hippocampus, as measured by c-fos mRNA induction, a proxy of neuronal activity following whisker stimulation. Moreover, resting-state fMRI showed a significantly reduced S1-hippocampal connectivity in Shank3b mutants, in the absence of altered connectivity between S1 and other somatosensory areas. Impaired crosstalk between hippocampus and S1 might underlie Shank3b(-/-) hypo-reactivity to whisker-dependent cues, highlighting a potentially generalizable somatosensory dysfunction in ASD.

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