Takesian, A. | Search bioRxiv

bioRxiv2024

Reliable sensory processing of superficial cortical interneurons is modulated by behavioral state

The GABAergic interneurons within cortical layer 1 (L1) integrate sensory and top-down inputs to modulate network activity and induce the plasticity underlying learning. However, little is known about how sensory inputs drive L1 interneuron activity. We used two-photon calcium imaging to measure the sound-evoked responses of two L1 interneuron populations expressing VIP (vasoactive intestinal peptide) or NDNF (neuron-derived neurotrophic factor) in mouse auditory cortex. We find that L1 interneurons respond to both simple and complex sounds with high trial-to-trial variability. However, these interneurons respond reliably to just a narrow range of stimuli, reflecting selectivity to spectrotemporal sound features. This response reliability is modulated by behavioral state and predicted by the activity of neighboring interneurons. Our data reveal that L1 interneurons exhibit sensory tuning and identify the modulation of response reliability as a potential mechanism by which L1 relays state-dependent cues to shape sensory representations.

neuroscience↗

bioRxiv2022

Neural signatures of auditory hypersensitivity following acoustic trauma

Throughout the brain, neurons exhibit a remarkable capacity to maintain stable firing rates despite large perturbations in afferent activity levels. As an exception, homeostatic regulation of neural activity often fails in the adult auditory system after hearing loss. Cochlear deafferentation caused by aging or noise exposure triggers widespread neural hyperactivity, particularly in the auditory cortex (ACtx), which underlies perceptual disorders including tinnitus and hyperacusis. Here, we show that mice with noise-induced damage of the high-frequency cochlear base were behaviorally hypersensitive to spared mid-frequency tones and to direct optogenetic stimulation of auditory thalamocortical neurons. Chronic 2-photon calcium imaging from ACtx pyramidal neurons (PyrNs) revealed an initial stage of diffuse hyperactivity, hypercorrelation, and hyperresponsivity that consolidated around deafferented map regions three or more days after acoustic trauma. Deafferented PyrN ensembles displayed hypersensitive decoding of spared mid-frequency tones, mirroring behavioral hypersensitivity. At the level of individual PyrNs, some exhibited stable, homeostatic gain control after acoustic trauma, while others showed non-homeostatic excess gain. Interestingly, factors such as baseline spontaneous activity levels and sound level encoding could account for 40% of the variability in PyrN gain regulation after acoustic trauma. These findings suggest that non-homeostatic regulation of cortical sound intensity coding following sensorineural loss may underlie the well-established clinical phenomenon of loudness hypersensitivity. Further, while cortical gain changes are triggered by reduced bottom-up afferent input, their subsequent stabilization is also shaped by their local circuit milieu, where baseline response features can identify neurons with the greatest propensity for developing pathological hyperactivity following sensorineural hearing loss.

neuroscience↗