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Mossing, D. P.

Publications and source records attributed to Mossing, D. P..

4 recordsLinked to original sources

VIP neurons desynchronize cortical assemblies

Gamma band synchronization can facilitate local and long-range communication in neural circuits. In the primary visual cortex (V1) the strength of synchronization on the local level is strongly tuned to the contrast, size and center/surround orientation of grating stimuli. On the global level, the synchronization of gamma oscillations across the retinotopic map crucially depends on matched stimulus properties in the corresponding locations in the visual field. Although these features of V1 gamma rhythms are likely to be crucial for how they might support cortico-cortical communication and visual perception, their neural basis remains largely unknown. We hypothesized VIP disinhibitory interneurons, which shape other tuning properties in V1 by inhibiting SST neurons, may be responsible for tuning local gamma band power and global gamma synchronization. To test these ideas, we combined multi-electrode electrophysiology, cell-type specific optogenetic suppression of VIP neurons and computational modeling. Contrary to expectations, our data show that on the local level, VIP activity has no role in tuning gamma power to stimulus properties; rather, it scales the gain of gamma oscillations linearly across stimulus space and across behavioral state. Conversely, on the global level, VIP neurons specifically suppress gamma synchronization (as measured by spectral coherence) between spatially separated cortical ensembles when they are processing non-matched stimulus features. A straightforward computational model of V1 shows that like-to-like connectivity across retinotopic space, and specific, but powerful VIPSST inhibition are sufficient to capture these seemingly opposed effects. These data demonstrate how VIP neurons differentially impact local and global properties of gamma rhythms depending on the global statistics of the retinal image. VIP neurons may thus construct temporal filters in the gamma band for spatially continuous image features, such as contours, to facilitate the downstream generation of coherent visual percepts.

neuroscience

Antagonistic inhibitory subnetworks control cooperation and competition across cortical space

The cortical microcircuit can dynamically adjust to dramatic changes in the strength, scale, and complexity of its input. In the primary visual cortex (V1), pyramidal cells (PCs) integrate widely across space when signals are weak, but narrowly when signals are strong, a phenomenon known as contrast-dependent surround suppression. Theoretical work has proposed that local interneurons could mediate a shift from cooperation to competition of PCs across cortical space, underlying this computation. We combined calcium imaging and electrophysiology to constrain a stabilized supralinear network model that explains how the four principal cell types in layer 2/3 (L2/3) of mouse V1- somatostatin (SST), parvalbumin (PV), and vasoactive intestinal peptide (VIP) interneurons, and PCs- transform inputs from layer 4 (L4) PCs to encode drifting gratings of varying size and contrast. Using bidirectional optogenetic perturbations, we confirmed key predictions of the model. Our data and modeling showed that recurrent amplification drives a transition from a positive PC[->]VIP{dashv}SST{dashv}PC feedback loop at small size and low contrast to a negative PC[->]SST{dashv}PC feedback loop at large size and high contrast to contribute to this flexible computation. This may represent a widespread mechanism for gating competition across cortical space to optimally meet task demands.

neuroscience

Structure and variability of optogenetic responses identify the operating regime of cortex

The visual cortex receives non-sensory inputs containing behavioral and brain state information. Here we propose a parallel between optogenetic and behavioral modulations of activity and characterize their impact on cell-type-specific V1 processing under a common theoretical framework. We infer cell-type-specific circuitry from large-scale V1 recordings and demonstrate that, given strong recurrent excitation, the cell-type-specific responses imply key aspects of the known connectivity. In the inferred models, parvalbumin-expressing (PV), but not other, interneurons have responses to perturbations that we show theoretically imply that their activity stabilizes the circuit. We infer inputs that explain locomotion-induced changes in firing rates and find that, contrary to hypotheses of simple disinhibition, locomotory drive to VIP cells and to SOM cells largely cancel, with enhancement of excitatory-cell visual responses likely due to direct locomotory drive to them. We show that this SOM/VIP cancellation is a property emerging from V1 connectivity structure.

neuroscience

Synthesis of higher order feature codes through stimulus-specific supra-linear summation

How cortical circuits build representations of complex objects is poorly understood. The massive dimensional expansion from the thalamus to the primary sensory cortex may enable sparse, comprehensive representations of higher order features to facilitate object identification. To generate such a code, cortical neurons must integrate broadly over space, yet simultaneously obtain sharp tuning to specific stimulus features. The logic of cortical integration that may synthesize such a sparse, high dimensional code for complex features is not known. To address this question, we probed the integration and population coding of higher order stimuli in the somatosensory and visual cortices of awake mice using two-photon calcium imaging across cortical layers. We found that somatosensory and visual cortical neurons sum highly specific combinations of sensory inputs supra-linearly, but integrate other inputs sub-linearly, leading to selective responses to higher order features. This integrative process generates a sparse, but comprehensive code for complex stimuli from the earliest stages of cortical processing. These results from multiple sensory modalities imply that input-specific supra-linear summation may represent a widespread cortical mechanism for the synthesis of higher order feature codes. This new mechanism may explain how the brain exploits the thalamocortical expansion of dimensionality to encode arbitrary complex features of sensory stimuli.

neuroscience