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1.
bioRxiv ; 2023 Sep 30.
Article in English | MEDLINE | ID: mdl-37808857

ABSTRACT

Atypical sensory processing in autism involves altered neural circuit function and neural coding in sensory cortex, but the nature of coding disruption is poorly understood. We characterized neural coding in L2/3 of whisker somatosensory cortex (S1) of Cntnap2-/- mice, an autism model with pronounced hypofunction of parvalbumin (PV) inhibitory circuits. We tested for both excess spiking, which is often hypothesized in autism models with reduced inhibition, and alterations in somatotopic coding, using c-fos immunostaining and 2-photon calcium imaging in awake mice. In Cntnap2-/- mice, c-fos-(+) neuron density was elevated in L2/3 of S1 under spontaneous activity conditions, but comparable to control mice after whisker stimulation, suggesting that sensory-evoked spiking was relatively normal. 2-photon GCaMP8m imaging in L2/3 pyramidal cells revealed no increase in whisker-evoked response magnitude, but instead showed multiple signs of degraded somatotopic coding. These included broadening of whisker tuning curves, blurring of the whisker map, and blunting of the point representation of each whisker. These altered properties were more pronounced in noisy than sparse sensory conditions. Tuning instability, assessed over 2-3 weeks of longitudinal imaging, was also significantly increased in Cntnap2-/- mice. Thus, Cntnap2-/- mice show no excess spiking, but a degraded and unstable tactile code in S1.

2.
Front Neurol ; 14: 1254297, 2023.
Article in English | MEDLINE | ID: mdl-37745660

ABSTRACT

Individuals with autism spectrum disorder (ASD) exhibit a diverse range of behavioral features and genetic backgrounds, but whether different genetic forms of autism involve convergent pathophysiology of brain function is unknown. Here, we analyze evidence for convergent deficits in neural circuit function across multiple transgenic mouse models of ASD. We focus on sensory areas of neocortex, where circuit differences may underlie atypical sensory processing, a central feature of autism. Many distinct circuit-level theories for ASD have been proposed, including increased excitation-inhibition (E-I) ratio and hyperexcitability, hypofunction of parvalbumin (PV) interneuron circuits, impaired homeostatic plasticity, degraded sensory coding, and others. We review these theories and assess the degree of convergence across ASD mouse models for each. Behaviorally, our analysis reveals that innate sensory detection behavior is heightened and sensory discrimination behavior is impaired across many ASD models. Neurophysiologically, PV hypofunction and increased E-I ratio are prevalent but only rarely generate hyperexcitability and excess spiking. Instead, sensory tuning and other aspects of neural coding are commonly degraded and may explain impaired discrimination behavior. Two distinct phenotypic clusters with opposing neural circuit signatures are evident across mouse models. Such clustering could suggest physiological subtypes of autism, which may facilitate the development of tailored therapeutic approaches.

3.
Curr Biol ; 33(16): 3398-3408.e7, 2023 08 21.
Article in English | MEDLINE | ID: mdl-37499665

ABSTRACT

Vasoactive intestinal peptide (VIP) interneurons in sensory cortex modulate sensory responses based on global exploratory behavior and arousal state, but their function during non-exploratory, goal-directed behavior is not well understood. In particular, whether VIP cells are activated by sensory cues, reward-seeking actions, or directly by reinforcement is unclear. We trained mice on a Go/NoGo whisker touch detection task that included a delay period and other features designed to separate sensory-evoked, action-related, and reward-related neural activity. Mice had to lick in response to a whisker stimulus to receive a variable-sized reward. Using two-photon calcium imaging, we measured ΔF/F responses of L2/3 VIP neurons in whisker somatosensory cortex (S1) during behavior. In both expert and novice mice, VIP cells were strongly activated by whisker stimuli and goal-directed actions (licking), but not by reinforcement. VIP cells showed somatotopic whisker tuning that was spatially organized relative to anatomical columns in S1, unlike lick-related signals which were spatially widespread. In expert mice, lick-related VIP responses were suppressed, not enhanced, when a reward was delivered, and the amount of suppression increased with reward size. This reward-related suppression was not seen in novice mice, where reward delivery was not yoked to licking. These results indicate that besides arousal and global state variables, VIP cells are activated by local sensory features and goal-directed actions, but not directly by reinforcement. Instead, our results are consistent with a role for VIP cells in encoding the expectation of reward associated with motor actions.


Subject(s)
Interneurons , Vasoactive Intestinal Peptide , Mice , Animals , Interneurons/physiology , Neurons/physiology , Somatosensory Cortex/physiology , Reward , Vibrissae/metabolism
4.
Nat Commun ; 13(1): 6611, 2022 11 03.
Article in English | MEDLINE | ID: mdl-36329010

ABSTRACT

Rodent sensory cortex contains salt-and-pepper maps of sensory features, whose structure is not fully known. Here we investigated the structure of the salt-and-pepper whisker somatotopic map among L2/3 pyramidal neurons in somatosensory cortex, in awake mice performing one-vs-all whisker discrimination. Neurons tuned for columnar (CW) and non-columnar (non-CW) whiskers were spatially intermixed, with co-tuned neurons forming local (20 µm) clusters. Whisker tuning was markedly unstable in expert mice, with 35-46% of pyramidal cells significantly shifting tuning over 5-18 days. Tuning instability was highly concentrated in non-CW tuned neurons, and thus was structured in the map. Instability of non-CW neurons was unchanged during chronic whisker paralysis and when mice discriminated individual whiskers, suggesting it is an inherent feature. Thus, L2/3 combines two distinct components: a stable columnar framework of CW-tuned cells that may promote spatial perceptual stability, plus an intermixed, non-columnar surround with highly unstable tuning.


Subject(s)
Somatosensory Cortex , Vibrissae , Mice , Animals , Vibrissae/physiology , Somatosensory Cortex/physiology , Neurons/physiology , Pyramidal Cells , Wakefulness , Rodentia
5.
Curr Biol ; 30(16): 3065-3074.e5, 2020 08 17.
Article in English | MEDLINE | ID: mdl-32531284

ABSTRACT

In rodent whisker sensation, whisker position signals, including whisking phase, are integrated with touch signals to enable spatially accurate tactile perception, but other functions of phase coding are unclear. We investigate how phase coding affects the neural coding of surface features during surface whisking. In mice performing rough-smooth discrimination, S1 units exhibit much stronger phase tuning during surface whisking than in prior studies of whisking in air. Among putative pyramidal cells, preferred phase tiles phase space, but protraction phases are strongly over-represented. Fast-spiking units are nearly all protraction tuned. This protraction bias increases the coding of stick-slip whisker events during protraction, suggesting that surface features are preferentially encoded during protraction. Correspondingly, protraction-tuned units encode rough-smooth texture better than retraction-tuned units and encode the precise spatial location of surface ridges with higher acuity. This suggests that protraction is the main information-gathering phase for high-resolution surface features, with phase coding organized to support this function.


Subject(s)
Exploratory Behavior/physiology , Neural Pathways/physiology , Somatosensory Cortex/physiology , Touch Perception/physiology , Touch/physiology , Vibrissae/physiology , Animals , Rodentia
6.
Sci Rep ; 9(1): 17413, 2019 Nov 19.
Article in English | MEDLINE | ID: mdl-31745244

ABSTRACT

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

7.
Elife ; 82019 08 16.
Article in English | MEDLINE | ID: mdl-31418693

ABSTRACT

Sensory maps in layer (L) 2/3 of rodent cortex lack precise functional column boundaries, and instead exhibit locally heterogeneous (salt-and-pepper) tuning superimposed on smooth global topography. Could this organization be a byproduct of impoverished experience in laboratory housing? We compared whisker map somatotopy in L2/3 and L4 excitatory cells of somatosensory (S1) cortex in normally housed vs. tactile-enriched mice, using GCaMP6s imaging. Normally housed mice had a dispersed, salt-and-pepper whisker map in L2/3, but L4 was more topographically precise. Enrichment (P21 to P46-71) sharpened whisker tuning and decreased, but did not abolish, local tuning heterogeneity. In L2/3, enrichment strengthened and sharpened whisker point representations, and created functional boundaries of tuning similarity and noise correlations at column edges. Thus, enrichment drives emergence of functional columnar topography in S1, and reduces local tuning heterogeneity. These changes predict better touch detection by neural populations within each column.


Subject(s)
Brain Mapping , Somatosensory Cortex/anatomy & histology , Somatosensory Cortex/physiology , Touch Perception , Vibrissae/physiology , Animals , Green Fluorescent Proteins/analysis , Mice , Staining and Labeling/methods
8.
Sci Rep ; 9(1): 12087, 2019 08 19.
Article in English | MEDLINE | ID: mdl-31427615

ABSTRACT

Spike sorting is the process of detecting and clustering action potential waveforms of putative single neurons from extracellular voltage recordings. Typically, spike detection uses a fixed voltage threshold and shadow period, but this approach often misses spikes during high firing rate epochs or noisy conditions. We developed a simple, data-driven spike detection method using a scaled form of template matching, based on the sliding cosine similarity between the extracellular voltage signal and mean spike waveforms of candidate single units. Performance was tested in whisker somatosensory cortex (S1) of anesthetized mice in vivo. The method consistently detected whisker-evoked spikes that were missed by the standard fixed threshold. Detection was improved most for spikes evoked by strong stimuli (40-70% increase), improved less for weaker stimuli, and unchanged for spontaneous spiking. This represents improved detection during spatiotemporally dense spiking, and yielded sharper sensory tuning estimates. We also benchmarked performance using computationally generated voltage data. Template matching detected ~85-90% of spikes compared to ~70% for the standard fixed threshold method, and was more tolerant to high firing rates and simulated recording noise. Thus, a simple template matching approach substantially improves detection of single-unit spiking for cortical physiology.


Subject(s)
Action Potentials/physiology , Neurons/physiology , Somatosensory Cortex/physiology , Vibrissae/physiology , Algorithms , Animals , Humans , Mice , Models, Neurological
9.
Nat Neurosci ; 22(9): 1438-1449, 2019 09.
Article in English | MEDLINE | ID: mdl-31332375

ABSTRACT

How the somatosensory cortex (S1) encodes complex patterns of touch, such as those that occur during tactile exploration, is poorly understood. In the mouse whisker S1, temporally dense stimulation of local whisker pairs revealed that most neurons are not classical single-whisker feature detectors, but instead are strongly tuned to two-whisker sequences that involve the columnar whisker (CW) and one specific surround whisker (SW), usually in a SW-leading-CW order. Tuning was spatiotemporally precise and diverse across cells, generating a rate code for local motion vectors defined by SW-CW combinations. Spatially asymmetric, sublinear suppression for suboptimal combinations and near-linearity for preferred combinations sharpened combination tuning relative to linearly predicted tuning. This resembles computation of motion direction selectivity in vision. SW-tuned neurons, misplaced in the classical whisker map, had the strongest combination tuning. Thus, each S1 column contains a rate code for local motion sequences involving the CW, thus providing a basis for higher-order feature extraction.


Subject(s)
Mechanoreceptors/cytology , Somatosensory Cortex/cytology , Touch Perception/physiology , Vibrissae/innervation , Animals , Mice , Touch/physiology
10.
Neuron ; 101(4): 648-661.e4, 2019 02 20.
Article in English | MEDLINE | ID: mdl-30679017

ABSTRACT

Distinct genetic forms of autism are hypothesized to share a common increase in excitation-inhibition (E-I) ratio in cerebral cortex, causing hyperexcitability and excess spiking. We provide a systematic test of this hypothesis across 4 mouse models (Fmr1-/y, Cntnap2-/-, 16p11.2del/+, Tsc2+/-), focusing on somatosensory cortex. All autism mutants showed reduced feedforward inhibition in layer 2/3 coupled with more modest, variable reduction in feedforward excitation, driving a common increase in E-I conductance ratio. Despite this, feedforward spiking, synaptic depolarization, and spontaneous spiking were largely normal. Modeling revealed that E and I conductance changes in each mutant were quantitatively matched to yield stable, not increased, synaptic depolarization for cells near spike threshold. Correspondingly, whisker-evoked spiking was not increased in vivo despite detectably reduced inhibition. Thus, elevated E-I ratio is a common circuit phenotype but appears to reflect homeostatic stabilization of synaptic drive rather than driving network hyperexcitability in autism.


Subject(s)
Autistic Disorder/physiopathology , Evoked Potentials, Somatosensory , Excitatory Postsynaptic Potentials , Inhibitory Postsynaptic Potentials , Somatosensory Cortex/physiopathology , Animals , Autistic Disorder/genetics , Chromosomes, Human, Pair 16/genetics , Fragile X Mental Retardation Protein/genetics , Humans , Male , Membrane Proteins/genetics , Mice , Mice, Inbred C57BL , Nerve Tissue Proteins/genetics , Somatosensory Cortex/physiology , Tuberous Sclerosis Complex 2 Protein/genetics
11.
Curr Opin Neurobiol ; 53: 50-56, 2018 12.
Article in English | MEDLINE | ID: mdl-29775823

ABSTRACT

That experience shapes sensory tuning in primary sensory cortex is well understood. But effective neural population codes depend on more than just sensory tuning. Recent population imaging and recording studies have characterized population codes in sensory cortex, and tracked how they change with sensory manipulations and training on perceptual learning tasks. These studies confirm sensory tuning changes, but also reveal other features of plasticity, including sensory gain modulation, restructuring of firing correlations, and differential routing of information to output pathways. Unexpectedly strong day-to-day variation exists in single-neuron sensory tuning, which stabilizes during learning. These are novel dimensions of plasticity in sensory cortex, which refine population codes during learning, but whose mechanisms are unknown.


Subject(s)
Learning/physiology , Neuronal Plasticity/physiology , Neurons/physiology , Perception/physiology , Sensorimotor Cortex/physiology , Animals , Humans
12.
Proc Natl Acad Sci U S A ; 115(20): 5277-5282, 2018 05 15.
Article in English | MEDLINE | ID: mdl-29712831

ABSTRACT

Neurons responding to different whiskers are spatially intermixed in the superficial layer 2/3 (L2/3) of the rodent barrel cortex, where a single whisker deflection activates a sparse, distributed neuronal population that spans multiple cortical columns. How the superficial layer of the rodent barrel cortex is organized to support such distributed sensory representations is not clear. In a computer model, we tested the hypothesis that sensory representations in L2/3 of the rodent barrel cortex are formed by activity propagation horizontally within L2/3 from a site of initial activation. The model explained the observed properties of L2/3 neurons, including the low average response probability in the majority of responding L2/3 neurons, and the existence of a small subset of reliably responding L2/3 neurons. Sparsely propagating traveling waves similar to those observed in L2/3 of the rodent barrel cortex occurred in the model only when a subnetwork of strongly connected neurons was immersed in a much larger network of weakly connected neurons.


Subject(s)
Neural Networks, Computer , Neural Pathways/physiology , Neurons/physiology , Somatosensory Cortex/physiology , Vibrissae/physiology , Action Potentials , Animals , Electric Stimulation , Rodentia
13.
J Neurosci ; 38(20): 4749-4761, 2018 05 16.
Article in English | MEDLINE | ID: mdl-29678876

ABSTRACT

Rapid plasticity of layer (L) 2/3 inhibitory circuits is an early step in sensory cortical map plasticity, but its cellular basis is unclear. We show that, in mice of either sex, 1 d whisker deprivation drives the rapid loss of L4-evoked feedforward inhibition and more modest loss of feedforward excitation in L2/3 pyramidal (PYR) cells, increasing the excitation-inhibition conductance ratio. Rapid disinhibition was due to reduced L4-evoked spiking by L2/3 parvalbumin (PV) interneurons, caused by reduced PV intrinsic excitability. This included elevated PV spike threshold, which is associated with an increase in low-threshold, voltage-activated delayed rectifier (presumed Kv1) and A-type potassium currents. Excitatory synaptic input and unitary inhibitory output of PV cells were unaffected. Functionally, the loss of feedforward inhibition and excitation was precisely coordinated in L2/3 PYR cells, so that peak feedforward synaptic depolarization remained stable. Thus, the rapid plasticity of PV intrinsic excitability offsets early weakening of excitatory circuits to homeostatically stabilize synaptic potentials in PYR cells of sensory cortex.SIGNIFICANCE STATEMENT Inhibitory circuits in cerebral cortex are highly plastic, but the cellular mechanisms and functional importance of this plasticity are incompletely understood. We show that brief (1 d) sensory deprivation rapidly weakens parvalbumin (PV) inhibitory circuits by reducing the intrinsic excitability of PV neurons. This involved a rapid increase in voltage-gated potassium conductances that control near-threshold spiking excitability. Functionally, the loss of PV-mediated feedforward inhibition in L2/3 pyramidal cells was precisely balanced with the separate loss of feedforward excitation, resulting in a net homeostatic stabilization of synaptic potentials. Thus, rapid plasticity of PV intrinsic excitability implements network-level homeostasis to stabilize synaptic potentials in sensory cortex.


Subject(s)
Parvalbumins/physiology , Somatosensory Cortex/physiology , Vibrissae/innervation , Vibrissae/physiology , Animals , Brain Mapping , Electrophysiological Phenomena , Evoked Potentials, Motor/physiology , Female , Homeostasis/physiology , Mice , Mice, Inbred C57BL , Neural Conduction/physiology , Neuronal Plasticity/physiology , Neurons/physiology , Optogenetics , Potassium Channels, Voltage-Gated/physiology , Pyramidal Cells/physiology , Somatosensory Cortex/cytology
14.
Handb Clin Neurol ; 151: 73-102, 2018.
Article in English | MEDLINE | ID: mdl-29519481

ABSTRACT

Somatosensory areas containing topographic maps of the body surface are a major feature of parietal cortex. In primates, parietal cortex contains four somatosensory areas, each with its own map, with the primary cutaneous map in area 3b. Rodents have at least three parietal somatosensory areas. Maps are not isomorphic to the body surface, but magnify behaviorally important skin regions, which include the hands and face in primates, and the whiskers in rodents. Within each map, intracortical circuits process tactile information, mediate spatial integration, and support active sensation. Maps may also contain fine-scale representations of touch submodalities, or direction of tactile motion. Functional representations are more overlapping than suggested by textbook depictions of map topography. The whisker map in rodent somatosensory cortex is a canonic system for studying cortical microcircuits, sensory coding, and map plasticity. Somatosensory maps are plastic throughout life in response to altered use or injury. This chapter reviews basic principles and recent findings in primate, human, and rodent somatosensory maps.


Subject(s)
Brain Mapping , Somatosensory Cortex/anatomy & histology , Animals , Face/innervation , Hand/innervation , Humans , Neuronal Plasticity/physiology , Primates , Rodentia , Somatosensory Cortex/physiology , Vibrissae/innervation
15.
Neuron ; 97(2): 418-433.e5, 2018 01 17.
Article in English | MEDLINE | ID: mdl-29307709

ABSTRACT

Tactile objects have both local geometry (shape) and broader macroscopic texture, but how these different spatial scales are simultaneously encoded during active touch is unknown. In the whisker system, we tested for a shared code based on localized whisker micromotions (stick-slips) and slip-evoked spikes. We trained mice to discriminate smooth from rough surfaces, including ridged gratings and sandpaper. Whisker slips locked to ridges and evoked temporally precise spikes (<10 ms jitter) in somatosensory cortex (S1) that could resolve ridges with ∼1 mm accuracy. Slip-sensitive neurons also encoded touch and texture. On rough surfaces, both slip-evoked spikes and an additional non-slip signal elevated mean firing rate, allowing accurate rough-smooth texture decoding from population firing rate. Eighteen percent of neurons were selective among rough surfaces. Thus, slips elicit spatially and temporally precise spiking in S1 that simultaneously encodes local shape (ridges) and is integrated into a macroscopic firing rate code for roughness.


Subject(s)
Neurons/physiology , Somatosensory Cortex/physiology , Touch Perception/physiology , Vibrissae/physiology , Action Potentials , Animals , Cues , Discrimination, Psychological/physiology , Mice , Motion , Surface Properties , Time Factors , Touch/physiology , Vibrissae/innervation
16.
Article in English | MEDLINE | ID: mdl-28093551

ABSTRACT

We compare the circuit and cellular mechanisms for homeostatic plasticity that have been discovered in rodent somatosensory (S1) and visual (V1) cortex. Both areas use similar mechanisms to restore mean firing rate after sensory deprivation. Two time scales of homeostasis are evident, with distinct mechanisms. Slow homeostasis occurs over several days, and is mediated by homeostatic synaptic scaling in excitatory networks and, in some cases, homeostatic adjustment of pyramidal cell intrinsic excitability. Fast homeostasis occurs within less than 1 day, and is mediated by rapid disinhibition, implemented by activity-dependent plasticity in parvalbumin interneuron circuits. These processes interact with Hebbian synaptic plasticity to maintain cortical firing rates during learned adjustments in sensory representations.This article is part of the themed issue 'Integrating Hebbian and homeostatic plasticity'.


Subject(s)
Homeostasis , Neuronal Plasticity , Somatosensory Cortex/physiology , Visual Cortex/physiology , Animals , Mice , Pyramidal Cells/physiology , Rats , Sensory Deprivation
17.
Article in English | MEDLINE | ID: mdl-28093552

ABSTRACT

We summarize here the results presented and subsequent discussion from the meeting on Integrating Hebbian and Homeostatic Plasticity at the Royal Society in April 2016. We first outline the major themes and results presented at the meeting. We next provide a synopsis of the outstanding questions that emerged from the discussion at the end of the meeting and finally suggest potential directions of research that we believe are most promising to develop an understanding of how these two forms of plasticity interact to facilitate functional changes in the brain.This article is part of the themed issue 'Integrating Hebbian and homeostatic plasticity'.


Subject(s)
Brain/physiology , Homeostasis , Neuronal Plasticity , Animals , Humans
18.
PLoS Biol ; 14(8): e1002549, 2016 08.
Article in English | MEDLINE | ID: mdl-27574970

ABSTRACT

Rodent whisker input consists of dense microvibration sequences that are often temporally integrated for perceptual discrimination. Whether primary somatosensory cortex (S1) participates in temporal integration is unknown. We trained rats to discriminate whisker impulse sequences that varied in single-impulse kinematics (5-20-ms time scale) and mean speed (150-ms time scale). Rats appeared to use the integrated feature, mean speed, to guide discrimination in this task, consistent with similar prior studies. Despite this, 52% of S1 units, including 73% of units in L4 and L2/3, encoded sequences at fast time scales (≤20 ms, mostly 5-10 ms), accurately reflecting single impulse kinematics. 17% of units, mostly in L5, showed weaker impulse responses and a slow firing rate increase during sequences. However, these units did not effectively integrate whisker impulses, but instead combined weak impulse responses with a distinct, slow signal correlated to behavioral choice. A neural decoder could identify sequences from fast unit spike trains and behavioral choice from slow units. Thus, S1 encoded fast time scale whisker input without substantial temporal integration across whisker impulses.


Subject(s)
Discrimination, Psychological/physiology , Reaction Time/physiology , Somatosensory Cortex/physiology , Vibrissae/physiology , Animals , Evoked Potentials, Somatosensory/physiology , Female , Neurons/physiology , Physical Stimulation , Rats, Long-Evans , Somatosensory Cortex/cytology , Touch Perception/physiology , Vibration , Vibrissae/innervation
19.
PLoS One ; 11(2): e0148227, 2016.
Article in English | MEDLINE | ID: mdl-26840956

ABSTRACT

Inhibitory synapse development in sensory neocortex is experience-dependent, with sustained sensory deprivation yielding fewer and weaker inhibitory synapses. Whether this represents arrest of synapse maturation, or a more complex set of processes, is unclear. To test this, we measured the dynamics of inhibitory synapse development in layer 4 of rat somatosensory cortex (S1) during continuous whisker deprivation from postnatal day 7, and in age-matched controls. In deprived columns, spontaneous miniature inhibitory postsynaptic currents (mIPSCs) and evoked IPSCs developed normally until P15, when IPSC amplitude transiently decreased, recovering by P16 despite ongoing deprivation. IPSCs remained normal until P22, when a second, sustained phase of weakening began. Delaying deprivation onset by 5 days prevented the P15 weakening. Both early and late phase weakening involved measurable reduction in IPSC amplitude relative to prior time points. Thus, deprivation appears to drive two distinct phases of active IPSC weakening, rather than simple arrest of synapse maturation.


Subject(s)
Inhibitory Postsynaptic Potentials/physiology , Neurons, Afferent/physiology , Sensory Deprivation/physiology , Somatosensory Cortex/physiology , Vibrissae/physiology , Animals , Neuronal Plasticity/physiology , Patch-Clamp Techniques , Rats , Rats, Long-Evans , Synapses/physiology
20.
J Neurosci ; 35(9): 3946-58, 2015 Mar 04.
Article in English | MEDLINE | ID: mdl-25740523

ABSTRACT

Layer (L)2 is a major output of primary sensory cortex that exhibits very sparse spiking, but the structure of sensory representation in L2 is not well understood. We combined two-photon calcium imaging with deflection of many whiskers to map whisker receptive fields, characterize sparse coding, and quantitatively define the point representation in L2 of mouse somatosensory cortex. Neurons within a column-sized imaging field showed surprisingly heterogeneous, salt-and-pepper tuning to many different whiskers. Single whisker deflection elicited low-probability spikes in highly distributed, shifting neural ensembles spanning multiple cortical columns. Whisker-evoked response probability correlated strongly with spontaneous firing rate, but weakly with tuning properties, indicating a spectrum of inherent responsiveness across pyramidal cells. L2 neurons projecting to motor and secondary somatosensory cortex differed in whisker tuning and responsiveness, and carried different amounts of information about columnar whisker deflection. From these data, we derive a quantitative, fine-scale picture of the distributed point representation in L2.


Subject(s)
Neural Pathways/anatomy & histology , Neural Pathways/physiology , Somatosensory Cortex/anatomy & histology , Somatosensory Cortex/physiology , Vibrissae/innervation , Animals , Brain Mapping , Glutamate Decarboxylase/genetics , Glutamate Decarboxylase/physiology , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Physical Stimulation
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