principal neurons

Circuit dysfunction and sensory processing in Fragile X Syndrome

To uncover the circuit-level alterations that underlie atypical sensory processing associated with autism, we have adopted a symptom-to-circuit approach in theFmr1-/- mouse model of Fragile X syndrome (FXS). Using a go/no-go task and in vivo 2-photon calcium imaging, we find that impaired visual discrimination in Fmr1-/- mice correlates with marked deficits in orientation tuning of principal neurons in primary visual cortex, and a decrease in the activity of parvalbumin (PV) interneurons. Restoring visually evoked activity in PV cells in Fmr1-/- mice with a chemogenetic (DREADD) strategy was sufficient to rescue their behavioural performance. Strikingly, human subjects with FXS exhibit similar impairments in visual discrimination as Fmr1-/- mice. These results suggest that manipulating inhibition may help sensory processing in FXS. More recently, we find that the ability of Fmr1-/- mice to perform the visual discrimination task is also drastically impaired in the presence of visual or auditory distractors, suggesting that sensory hypersensitivity may affect perceptual learning in autism.

Evidence for electrical coupling between proximal axons of principal neurons

The seminar will present the origin of the hypothesis of electrical coupling between proximal axons, physiological and immunostaining evidence for the presence of the requisite gap junctions and will explain how electrical coupling could account for very fast network oscillations at >80 hz.

Analysis of the intraamygdalar connectivity and morphological characterization of principal neurons in the basolateral amygdala

Excessive midbrain glutamatergic tone promote anxiety via dysregulation of amygdala principal neurons

Diversity and connectivity of principal neurons in the lateral and basal nuclei of the mouse amygdala

FENS Forum 2024

Functional upregulation of KCC2 in cortical interneurons precedes that in glutamatergic principal neurons

FENS Forum 2024