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Garderes, P.-M.

Publications and source records attributed to Garderes, P.-M..

3 recordsLinked to original sources

Distinct laminar origins of high-gamma and low-frequency ECoG signals revealed by optogenetics

Electrocorticography (ECoG) provides a high-spatiotemporal-resolution measure of cortical activity (cortical surface electrical potentials, CSEPs) in humans and animals. The CSEP high-gamma band (H{gamma}, 65-170 Hz) correlates with neuronal firing rates at the columnar spatial scale and is widely used as a biomarker of local activity. Whether H{gamma} reports all stages of columnar processing, intermediate processing in L2/3 (close to the ECoG electrode), or the main columnar output in L5, is unknown. We disentangled the laminar origins of H{gamma} and other ECoG bands by optogenetically suppressing L2/3 or L5 pyramidal cells during micro-ECoG recording in mouse somatosensory cortex. Whisker deflections evoked transient, topographically localized CSEPs. L5 optogenetic suppression most strongly reduced 65-450 Hz (H{gamma}-uH{gamma}) bands in sensory-evoked ECoG signals, whereas L2/3 suppression most strongly reduced 4-30 Hz ({theta}-{beta}) bands. Thus, different CSEP frequency bands reflect layer-specific activity and are biomarkers of distinct stages of columnar processing. Significance StatementElectrocorticography (ECoG) is widely used as a mesoscale measure of cortical activity in human and animals, providing a unique methodological from basic neuroscience discovery to understanding the human brain in health and disease. However, the cell types and laminar sources that generate ECoG signals are unknown, which impedes interpretation of ECoG findings in both the clinic and basic research. We disentangled the laminar origins of ECoG frequency bands by optogenetically suppressing L2/3 or L5 pyramidal cells during ECoG recording in mouse somatosensory cortex. We found that L5 optogenetic suppression most strongly reduced high frequencies whereas L2/3 suppression most strongly reduced lower frequencies. Thus, different ECoG frequency bands reflect layer-specific activity and are biomarkers of distinct stages of columnar processing.

neuroscience↗

Coexistence of state, choice, and sensory integration coding in barrel cortex LII/III

During perceptually guided decisions, correlates of choice are found as upstream as in the primary sensory areas. However, how well these choice signals align with early sensory representations, a prerequisite for their interpretation as feedforward substrates of perception, remains an open question. We designed a two alternative forced choice task (2AFC) in which mice compared stimulation frequencies applied to two adjacent vibrissae. The optogenetic silencing of individual columns in the primary somatosensory cortex (wS1) resulted in predicted shifts of psychometric functions, demonstrating that perception depends on focal, early sensory representations. Functional imaging of layer II/III single neurons revealed sensory, choice and engagement coding. From trial to trial, these three varied substantially, but independently from one another. Thus, coding of sensory and non-sensory variables co-exist in orthogonal subspace of the population activity, suggesting that perceptual variability does not originate from wS1 but rather from state or choice fluctuations in downstream areas.

neuroscience↗

Functional and structural properties of highly responsive somatosensory neurons in mouse barrel cortex

Sparse population activity is a hallmark of supra-granular sensory neurons in neocortex. The mechanisms underlying sparseness are not well understood because a direct link between the neurons activated in vivo and their cellular properties investigated in vitro has been missing. We used two-photon calcium imaging to identify a subset of neurons in layer L2/3 (L2/3) of mouse primary somatosensory cortex that are highly active following principal whisker vibrotactile stimulation. These high responders were then tagged using photoconvertible green fluorescent protein for subsequent targeting in the brain slice using intracellular patch-clamp recordings and biocytin staining. This approach allowed us to investigate the structural and functional properties of high responders that distinguish them from less active control cells. Compared to less responsive L2/3 neurons, high responders displayed increased levels of stimulus-evoked and spontaneous activity, elevated noise and spontaneous pair-wise correlations, and stronger coupling to the population response. Intrinsic excitability was reduced in high responders, while other electrophysiological and morphological parameters were unchanged. Thus, the choice of which neurons participate in stimulus encoding may largely be determined by network connectivity rather than by cellular structure and function.

neuroscience↗