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Deep feedforward and recurrent neural networks have become successful functional models of the brain, but they neglect obvious biological details such as spikes and Dale's law. Here we argue that these details are crucial in order to understand how real neural circuits operate. Towards this aim, we put forth a new framework for spike-based computation in low-rank excitatory-inhibitory spiking networks. By considering populations with rank-1 connectivity, we cast each neuron's spiking threshold as a boundary in a low-dimensional input-output space. We then show how the combined thresholds of a population of inhibitory neurons form a stable boundary in this space, and those of a population of excitatory neurons form an unstable boundary. Combining the two boundaries results in a rank-2 excitatory-inhibitory (EI) network with inhibition-stabilized dynamics at the intersection of the two boundaries. The computation of the resulting networks can be understood as the difference of two convex functions and is thereby capable of approximating arbitrary non-linear input-output mappings. We demonstrate several properties of these networks, including noise suppression and amplification, irregular activity and synaptic balance, as well as how they relate to rate network dynamics in the limit that the boundary becomes soft. Finally, while our work focuses on small networks (5-50 neurons), we discuss potential avenues for scaling up to much larger networks. Overall, our work proposes a new perspective on spiking networks that may serve as a starting point for a mechanistic understanding of biological spike-based computation. [ABSTRACT FROM AUTHOR]

• Linear dimensionality reduction methods provide neat summaries of population responses. • Demixing methods additionally demix responses relative to experimental parameters. • Smooth mappings of experimental parameters onto flat neural manifolds boost demixability. • Neural networks with low-rank connectivities can produce demixed manifolds. A central tenet of neuroscience is that the brain works through large populations of interacting neurons. With recent advances in recording techniques, the inner working of these populations has come into full view. Analyzing the resulting large-scale data sets is challenging because of the often complex and 'mixed' dependency of neural activities on experimental parameters, such as stimuli, decisions, or motor responses. Here we review recent insights gained from analyzing these data with dimensionality reduction methods that 'demix' these dependencies. We demonstrate that the mappings from (carefully chosen) experimental parameters to population activities appear to be typical and stable across tasks, brain areas, and animals, and are often identifiable by linear methods. By considering when and why dimensionality reduction and demixing work well, we argue for a view of population coding in which populations represent (demixed) latent signals, corresponding to stimuli, decisions, motor responses, and so on. These latent signals are encoded into neural population activity via non-linear mappings and decoded via linear readouts. We explain how such a scheme can facilitate the propagation of information across cortical areas, and we review neural network architectures that can reproduce the encoding and decoding of latent signals in population activities. These architectures promise a link from the biophysics of single neurons to the activities of neural populations. [ABSTRACT FROM AUTHOR]

All of our perceptual experiences arise from the activity of neural populations. Here we study the formation of such percepts under the assumption that they emerge from a linear readout, i.e., a weighted sum of the neurons’ firing rates. We show that this assumption constrains the trial-to-trial covariance structure of neural activities and animal behavior. The predicted covariance structure depends on the readout parameters, and in particular on the temporal integration window w and typical number of neurons K used in the formation of the percept. Using these predictions, we show how to infer the readout parameters from joint measurements of a subject’s behavior and neural activities. We consider three such scenarios: (1) recordings from the complete neural population, (2) recordings of neuronal sub-ensembles whose size exceeds K, and (3) recordings of neuronal sub-ensembles that are smaller than K. Using theoretical arguments and artificially generated data, we show that the first two scenarios allow us to recover the typical spatial and temporal scales of the readout. In the third scenario, we show that the readout parameters can only be recovered by making additional assumptions about the structure of the full population activity. Our work provides the first thorough interpretation of (feed-forward) percept formation from a population of sensory neurons. We discuss applications to experimental recordings in classic sensory decision-making tasks, which will hopefully provide new insights into the nature of perceptual integration. [ABSTRACT FROM AUTHOR]

Highlights: [•] Insufficient knowledge by the experimenter results in neural variability. [•] What counts as variability for the experimenter and for the organism may be different. [•] The sources of variability can be targeted through modeling studies. [•] Variability may have an adaptive functional role. [ABSTRACT FROM AUTHOR]

Two observations about the cortex have puzzled neuroscientists for a long time. First, neural responses are highly variable. Second, the level of excitation and inhibition received by each neuron is tightly balanced at all times. Here, we demonstrate that both properties are necessary consequences of neural networks that represent information efficiently in their spikes. We illustrate this insight with spiking networks that represent dynamical variables. Our approach is based on two assumptions: We assume that information about dynamical variables can be read out linearly from neural spike trains, and we assume that neurons only fire a spike if that improves the representation of the dynamical variables. Based on these assumptions, we derive a network of leaky integrate-and-fire neurons that is able to implement arbitrary linear dynamical systems. We show that the membrane voltage of the neurons is equivalent to a prediction error about a common population-level signal. Among other things, our approach allows us to construct an integrator network of spiking neurons that is robust against many perturbations. Most importantly, neural variability in our networks cannot be equated to noise. Despite exhibiting the same single unit properties as widely used population code models (e.g. tuning curves, Poisson distributed spike trains), balanced networks are orders of magnitudes more reliable. Our approach suggests that spikes do matter when considering how the brain computes, and that the reliability of cortical representations could have been strongly underestimated. [ABSTRACT FROM AUTHOR]

Typically, neurons in sensory areas are highly interconnected. Coupling two neurons can synchronize their activity and affect a variety of single-cell properties, such as their stimulus tuning, firing rate or gain. All of these factors must be considered to understand how two neurons should be coupled to optimally process stimuli. We quantified the functional effect of an interaction between two optic-flow processing neurons (Vi and H1) in the fly (Lucilia sericata). Using a generative model, we estimated a uni-directional coupling from H1 to Vi. Especially at a low signal-to-noise ratio (SNR), the coupling strongly improved the information about optic-flow in Vi. We identified two constraints confining the strength of the interaction. First, for weak couplings, Vi benefited from inputs by H1 without a concomitant shift of its stimulus tuning. Second, at both low and high SNR, the coupling strength lay in a range in which the information carried by single spikes is optimal. [ABSTRACT FROM AUTHOR]

Summary: A central goal in sensory neuroscience is to fully characterize a neuron''s input-output relation. However, strong nonlinearities in the responses of sensory neurons have made it difficult to develop models that generalize to arbitrary stimuli. Typically, the standard linear-nonlinear models break down when neurons exhibit stimulus-dependent modulations of their gain or selectivity. We studied these issues in optic-flow processing neurons in the fly. We found that the neurons'' receptive fields are fully described by a time-varying vector field that is space-time separable. Increasing the stimulus strength, however, strongly reduces the neurons'' gain and selectivity. To capture these changes in response behavior, we extended the linear-nonlinear model by a biophysically motivated gain and selectivity mechanism. We fit all model parameters directly to the data and show that the model now characterizes the neurons'' input-output relation well over the full range of motion stimuli. [Copyright &y& Elsevier]

How does the brain store information over a short period of time? Typically, the short-term memory of items or values is thought to be stored in the persistent activity of neurons in higher cortical areas. However, the activity of these neurons often varies strongly in time, even if time is unimportant for whether or not rewards are received. To elucidate this interaction of time and memory, we reexamined the activity of neurons in the prefrontal cortex of monkeys performing a working memory task. As often observed in higher cortical areas, different neurons have highly heterogeneous patterns of activity, making interpretation of the data difficult. To overcome these problems, we developed a method that finds a new representation of the data in which heterogeneity is much reduced, and time- and memory-related activities became separate and easily interpretable. This new representation consists of a few fundamental activity components that capture 95%of the firing rate variance of >800 neurons. Surprisingly, the memory-related activity components account for <20% of this firing rate variance. The observed heterogeneity of neural responses results from random combinations of these fundamental components. Based on these components, we constructed a generative linear model of the network activity. The model suggests that the representations of time and memory are maintained by separate mechanisms, even while sharing a common anatomical substrate. Testable predictions of this hypothesis are proposed. We suggest that our method may be applied to data from other tasks in which neural responses are highly heterogeneous across neurons, and dependent on more than one variable. [ABSTRACT FROM AUTHOR]

Neurons that sustain elevated firing in the absence of stimuli have been found in many neural systems. In graded persistent activity, neurons can sustain firing at many levels, suggesting a widely found type of network dynamics in which networks can relax to any one of a continuum of stationary states. The reproduction of these findings in model networks of nonlinear neurons has turned out to be nontrivial. A particularly insightful model has been the "bump attractor," in which a continuous attractor emerges through an underlying symmetry in the network connectivity matrix. This model, however, cannot account for data in which the persistent firing of neurons is a monotonic-rather than a bell-shaped-function of a stored variable. Here, we show that the symmetry used in the bump attractor network can be employed to create a whole family of continuous attractor networks, including those with monotonic tuning. Our design is based on tuning the external inputs to networks that have a connectivity matrix with Toeplitz symmetry. In particular, we provide a complete analytical solution of a line attractor network with monotonic tuning and show that for many other networks, the numerical tuning of synaptic weights reduces to the computation of a single parameter. [ABSTRACT FROM AUTHOR]

Summary: According to Barlow’s seminal “efficient coding hypothesis,” the coding strategy of sensory neurons should be matched to the statistics of stimuli that occur in an animal’s natural habitat. Using an automatic search technique, we here test this hypothesis and identify stimulus ensembles that sensory neurons are optimized for. Focusing on grasshopper auditory receptor neurons, we find that their optimal stimulus ensembles differ from the natural environment, but largely overlap with a behaviorally important sub-ensemble of the natural sounds. This indicates that the receptors are optimized for peak rather than average performance. More generally, our results suggest that the coding strategies of sensory neurons are heavily influenced by differences in behavioral relevance among natural stimuli. [Copyright &y& Elsevier]

Networks adapt to environmental demands by switching betweendistinct dynamical behaviors. The activity of frontal-lobe neuronsduring two-interval discrimination tasks is an example of theseadaptable dynamics. Subjects first perceive a stimulus, then hold it inworking memory, and finally make a decision by comparing it with asecond stimulus. We present a simple mutualinhibition network model thatcaptures all three task phases within a single framework. The modelintegrates both working memory and decision making because its dynamicalproperties are easily controlled without changing its connectivity.Mutual inhibition between nonlinear units is a useful design motif fornetworks that must display multiple behaviors. [ABSTRACT FROM AUTHOR]

How do cortical neurons represent the acoustic environment? This question is often addressed by probing with simple stimuli such as clicks or tone pips. Such stimuli have the advantage of yielding easily interpreted answers, but have the disadvantage that they may fail to uncover complex or higher-order neuronal response properties. Here, we adopt an alternative approach, probing neuronal responses with complex acoustic stimuli, including animal vocalizations. We used in vivo whole-cell methods in the rat auditory cortex to record subthreshold membrane potential fluctuations elicited by these stimuli. Most neurons responded robustly and reliably to the complex stimuli in our ensemble. Using regularization techniques, we estimated the linear component, the spectrotemporal receptive field (STRF), of the transformation from the sound (as represented by its time-varying spectrogram) to the membrane potential of the neuron. We find that the STRF has a rich dynamical structure, including excitatory regions positioned in general accord with the prediction of the classical tuning curve. However, whereas the STRF successfully predicts the responses to some of the natural stimuli, it surprisingly fails completely to predict the responses to others; on average, only 11% of the response power could be predicted by the STRF. Therefore, most of the response of the neuron cannot be predicted by the linear component, although the response is deterministically related to the stimulus. Analysis of the systematic errors of the STRF model shows that this failure cannot be attributed to simple nonlinearities such as adaptation to mean intensity, rectification, or saturation. Rather, the highly nonlinear response properties of auditory cortical neurons must be attributable to nonlinear interactions between sound frequencies and time-varying properties of the neural encoder. [ABSTRACT FROM AUTHOR]

We investigate the energy efficiency of signaling mechanisms that transfer information by means of discrete stochastic events, such as the opening or closing of an ion channel. Using a simple model for the generation of graded electrical signals by sodium and potassium channels, we find optimum numbers of channels that maximize energy efficiency. The optima depend on several factors: the relative magnitudes of the signaling cost (current flow through channels), the fixed cost of maintaining the system, the reliability of the input, additional sources of noise, and the relative costs of upstream and downstream mechanisms. We also analyze how the statistics of input signals influence energy efficiency. We find that energy-efficient signal ensembles favor a bimodal distribution of channel activations and contain only a very small fraction of large inputs when energy is scarce. We conclude that when energy use is a significant constraint, trade-offs between information transfer and energy can strongly influence the number of signaling molecules and synapses used by neurons and the manner in which these mechanisms represent information. [ABSTRACT FROM AUTHOR]

• A fundamental question in neuroscience is how neuronal populations in different brain areas communicate. • Multi-area neuronal population recordings are increasingly common. • Multivariate methods are needed to interrogate these recordings and characterize how neuronal population activity is related across areas. • We discuss interpretational challenges and considerations for these methods, and suggest directions for future work. The brain is composed of many functionally distinct areas. This organization supports distributed processing, and requires the coordination of signals across areas. Our understanding of how populations of neurons in different areas interact with each other is still in its infancy. As the availability of recordings from large populations of neurons across multiple brain areas increases, so does the need for statistical methods that are well suited for dissecting and interrogating these recordings. Here we review multivariate statistical methods that have been, or could be, applied to this class of recordings. By leveraging population responses, these methods can provide a rich description of inter-areal interactions. At the same time, these methods can introduce interpretational challenges. We thus conclude by discussing how to interpret the outputs of these methods to further our understanding of inter-areal interactions. [ABSTRACT FROM AUTHOR]

An abstract of the article "Network oscillations in a neural mass model induced by metabolic modulation are consistent with EEG data of neocortical epileptic seizure onset" by Florian A. Dehmelt and Christian K. Machens is presented.

The article focuses on the connection between neural readout weights and the perceptual decision. It states the researcher R. M. Hafner and colleagues have derived solutions on the connection of choice probability and the readout weights through the use of computer simulations. It mentions the insights of Haefner and colleagues concerning the formula of choice probability, such as the concept of optimality and the reconstruction of information of readout weights.

The article discusses a computational model of the human brain capable of simulating complex behaviors developed by C. Eliasmith et al. Eliasmith and colleagues' model, which is called the Semantic Pointer Architecture Unified Network (Spaun), can observe visual images and indicate its responses with a physical model of an arm. Topics include the challenges of building an artificial brain, such as the complexity of the human brain, the range of tasks Spaun can perform, such as image recognition, and an overview of the cognitive machinery of Spaun.

Introduces the December 2003 issue of the periodical "Journal of Neurophysiology." Extended Fishbach, Nelken and Yeshurun (FNY) auditory cortex model; Simplicity of the extended FNY model; Topographical organization of the FNY model.

Animals that rely on acoustic communication to find mates, such as grasshoppers, are astonishingly accurate in recognizing song patterns that are specific to their own species. This raises the question of whether they can also solve a far more complicated task that might provide a basis for mate preference and sexual selection: to distinguish individual songs by detecting slight variations around the common species-specific theme. Using spike-train discriminability to quantify the precision of neural responses from the auditory periphery of a model grasshopper species, we show that information sufficient to distinguish songs is readily available at the single-cell level when the spike trains are analyzed on a millisecond time scale. [ABSTRACT FROM AUTHOR]

The brain has an impressive ability to withstand neural damage. Diseases that kill neurons can go unnoticed for years, and incomplete brain lesions or silencing of neurons often fail to produce any behavioral effect. How does the brain compensate for such damage, and what are the limits of this compensation? We propose that neural circuits immediately com pensate for neuron loss, thereby preserving their function as much as possible. We show that this compensation can explain changes in tuning curves induced by neuron silencing across a variety of systems, including the primary visual cortex. We find that compensatory mechanisms can be implemented through the dynamics of networks with a tight balance of excitation and inhibition, without requiring synaptic plasticity. The limits of this compen satory mechanism are reached when excitation and inhibition become unbalanced, thereby demarcating a recovery boundary, where signal representation fails and where diseases may become symptomatic. [ABSTRACT FROM AUTHOR]

Neural systems are remarkably robust against various perturbations, a phenomenon that still requires a clear explanation. Here, we graphically illustrate how neural networks can become robust. We study spiking networks that generate low-dimensional representations, and we show that the neurons' subthreshold voltages are confined to a convex region in a lower-dimensional voltage subspace, which we call a 'bounding box'. Any changes in network parameters (such as number of neurons, dimensionality of inputs, firing thresholds, synaptic weights, or transmission delays) can all be understood as deformations of this bounding box. Using these insights, we show that functionality is preserved as long as perturbations do not destroy the integrity of the bounding box. We suggest that the principles underlying robustness in these networks -- low-dimensional representations, heterogeneity of tuning, and precise negative feedback -- may be key to understanding the robustness of neural systems at the circuit level. [ABSTRACT FROM AUTHOR]

Abstract: Cortical activity involves large populations of neurons, even when it is limited to functionally coherent areas. Electrophysiological recordings, on the other hand, involve comparatively small neural ensembles, even when modern-day techniques are used. Here we review results which have started to fill the gap between these two scales of inquiry, by shedding light on the statistical distributions of activity in large populations of cells. We put our main focus on data recorded in awake animals that perform simple decision-making tasks and consider statistical distributions of activity throughout cortex, across sensory, associative, and motor areas. We transversally review the complexity of these distributions, from distributions of firing rates and metrics of spike-train structure, through distributions of tuning to stimuli or actions and of choice signals, and finally the dynamical evolution of neural population activity and the distributions of (pairwise) neural interactions. This approach reveals shared patterns of statistical organization across cortex, including: (i) long-tailed distributions of activity, where quasi-silence seems to be the rule for a majority of neurons; that are barely distinguishable between spontaneous and active states; (ii) distributions of tuning parameters for sensory (and motor) variables, which show an extensive extrapolation and fragmentation of their representations in the periphery; and (iii) population-wide dynamics that reveal rotations of internal representations over time, whose traces can be found both in stimulus-driven and internally generated activity. We discuss how these insights are leading us away from the notion of discrete classes of cells, and are acting as powerful constraints on theories and models of cortical organization and population coding. [Copyright &y& Elsevier]

Sensory systems extract behaviorally relevant information from a continuous stream of complex high-dimensional input signals. Understanding the detailed dynamics and precise neural code, even of a single neuron, is therefore a non-trivial task. Automated closed-loop approaches that integrate data analysis in the experimental design ease the investigation of sensory systems in three directions: First, adaptive sampling speeds up the data acquisition and thus increases the yield of an experiment. Second, model-driven stimulus exploration improves the quality of experimental data needed to discriminate between alternative hypotheses. Third, information-theoretic data analyses open up novel ways to search for those stimuli that are most efficient in driving a given neuron in terms of its firing rate or coding quality. Examples from different sensory systems show that, in all three directions, substantial progress can be achieved once rapid online data analysis, adaptive sampling, and computational modeling are tightly integrated into experiments. [Copyright &y& Elsevier]

The fundamental building block of every nervous system is the single neuron. Understanding how these exquisitely structured elements operate is an integral part of the quest to solve the mysteries of the brain. Quantitative mathematical models have proved to be an indispensable tool in pursuing this goal. We review recent advances and examine how single-cell models on five levels of complexity, from black-box approaches to detailed compartmental simulations, address key questions about neural dynamics and signal processing. [ABSTRACT FROM AUTHOR]

Nearly all brain functions involve routing neural activity among a distributed network of areas. Understanding this routing requires more than a description of interareal anatomical connectivity: it requires understanding what controls the flow of signals through interareal circuitry and how this communication might be modulated to allow flexible behavior. Here we review proposals of how communication, particularly between visual cortical areas, is instantiated and modulated, highlighting recent work that offers new perspectives. We suggest transitioning from a focus on assessing changes in the strength of interareal interactions, as often seen in studies of interareal communication, to a broader consideration of how different signaling schemes might contribute to computation. To this end, we discuss a set of features that might be desirable for a communication scheme. Corticocortical communication is a fundamental aspect of brain function. Flexible behavior suggests a need for modulating interareal signaling from moment to moment. Several schemes for modulating corticocortical communication have been proposed. These include altering the structure of activity within a source network, the sensitivity of a target network to the input it receives, or gating signals during the relay between areas. We review these schemes and highlight new proposals that suggest communication may be determined by how source population signals align with interareal communication subspaces. We propose a set of design considerations for evaluating the relative merits of different communication schemes. When examining interareal communication, we suggest moving beyond merely characterizing changes in the strength of interareal interactions, to a wider consideration of the computational benefits and limitations of different communication schemes. [ABSTRACT FROM AUTHOR]

Networks based on coordinated spike coding can encode information with high efficiency in the spike trains of individual neurons. These networks exhibit single-neuron variability and tuning curves as typically observed in cortex, but paradoxically coincide with a precise, non-redundant spike-based population code. However, it has remained unclear whether the specific synaptic connectivities required in these networks can be learnt with local learning rules. Here, we show how to learn the required architecture. Use coding efficiency as an objective, we derive spike-timing-dependent learning rules for a recurrent neural network, and we provide exact solutions for the networks' convergence to an optimal state. As a result, we deduce an entire network from its input distribution and a firing cost. After learning, basic biophysical quantities such as voltages, firing thresholds, excitation, inhibition, or spikes acquire precise functional interpretations. Author summary: Spiking neural networks can encode information with high efficiency in the spike trains of individual neurons if the synaptic weights between neurons are set to specific, optimal values. In this regime, the networks exhibit irregular spike trains, high trial-to-trial variability, and stimulus tuning as typically observed in cortex. The strong variability on the level of single neurons paradoxically coincides with a precise, non-redundant spike-based population code. However, it has remained unclear whether the specific synaptic connectivities required in these spiking networks can be learnt with local learning rules. In this study, we show how the required architecture can be learnt. We derive local and biophysically plausible learning rules for a recurrent neural networks from first principles. We show both mathematically and using numerical simulations that these learning rules drive the networks into the optimal state, and we show that the optimal state is governed by the statistics of the input signals. After learning, the voltages of individual neurons can be interpreted as measuring the instantaneous error of the code, given by the error between the desired output signal and the actual output signal. [ABSTRACT FROM AUTHOR]

In many brain areas, neuronal activity is associated with a variety of behavioral and environmental variables. In particular, neuronal responses in the zebrafish hindbrain relate to oculomotor and swimming variables as well as sensory information. However, the precise functional organization of the neurons has been difficult to unravel because neuronal responses are heterogeneous. Here, we used dimensionality reduction methods on neuronal population data to reveal the role of the hindbrain in visually driven oculomotor behavior and swimming. We imaged neuronal activity in zebrafish expressing GCaMP6s in the nucleus of almost all neurons while monitoring the behavioral response to gratings that rotated with different speeds. We then used reduced-rank regression, a method that condenses the sensory and motor variables into a smaller number of "features," to predict the fluorescence traces of all ROIs (regions of interest). Despite the potential complexity of the visuo-motor transformation, our analysis revealed that a large fraction of the population activity can be explained by only two features. Based on the contribution of these features to each ROI's activity, ROIs formed three clusters. One cluster was related to vergent movements and swimming, whereas the other two clusters related to leftward and rightward rotation. Voxels corresponding to these clusters were segregated anatomically, with leftward and rightward rotation clusters located selectively to the left and right hemispheres, respectively. Just as described in many cortical areas, our analysis revealed that single-neuron complexity co-exists with a simpler population-level description, thereby providing insights into the organization of visuo-motor transformations in the hindbrain. [Display omitted] • Bilaterally independent visual stimuli decouple eye movements and elicit swimming • In the dorsal hindbrain, activity related to the eyes and tail is low dimensional • Neurons form clusters related to vergent and left/right rotational movements • Rotation and vergence clusters have distinct anatomical organization Feierstein et al. use visual stimuli that elicit decoupled eye movements and swimming in zebrafish larvae. Combining regression and dimensionality reduction techniques, they show that behavior-related activity in the hindbrain is low dimensional. Neurons form functional and spatial clusters related to vergent and rotational movements. [ABSTRACT FROM AUTHOR]

Summary Most brain functions involve interactions among multiple, distinct areas or nuclei. For instance, visual processing in primates requires the appropriate relaying of signals across many distinct cortical areas. Yet our understanding of how populations of neurons in interconnected brain areas communicate is in its infancy. Here we investigate how trial-to-trial fluctuations of population responses in primary visual cortex (V1) are related to simultaneously recorded population responses in area V2. Using dimensionality reduction methods, we find that V1-V2 interactions occur through a communication subspace: V2 fluctuations are related to a small subset of V1 population activity patterns, distinct from the largest fluctuations shared among neurons within V1. In contrast, interactions between subpopulations within V1 are less selective. We propose that the communication subspace may be a general, population-level mechanism by which activity can be selectively routed across brain areas. Highlights • Visual cortical areas interact through a communication subspace (CS) • The CS defines which activity patterns in a source area relate to downstream activity • The largest activity patterns in a source area are not matched to the CS • The CS allows for selective and flexible routing of population signals between areas Most brain functions require the selective and flexible routing of neuronal activity between cortical areas. Using paired population recordings from multiple visual cortical areas, Semedo et al. find a population-level mechanism that can achieve this routing, termed a communication subspace. [ABSTRACT FROM AUTHOR]

An abstract of the article "Positive sparse coding of natural images: a theory for simple cell tuning" by David G. T. Barrett, Sophie Denève and Christian K. Machens is presented.

Summary Dopamine neurons encode the difference between actual and predicted reward, or reward prediction error (RPE). Although many models have been proposed to account for this computation, it has been difficult to test these models experimentally. Here we established an awake electrophysiological recording system, combined with rabies virus and optogenetic cell-type identification, to characterize the firing patterns of monosynaptic inputs to dopamine neurons while mice performed classical conditioning tasks. We found that each variable required to compute RPE, including actual and predicted reward, was distributed in input neurons in multiple brain areas. Further, many input neurons across brain areas signaled combinations of these variables. These results demonstrate that even simple arithmetic computations such as RPE are not localized in specific brain areas but, rather, distributed across multiple nodes in a brain-wide network. Our systematic method to examine both activity and connectivity revealed unexpected redundancy for a simple computation in the brain. [ABSTRACT FROM AUTHOR]

Neurons in higher cortical areas, such as the prefrontal cortex, are often tuned to a variety of sensory and motor variables, and are therefore said to display mixed selectivity. This complexity of single neuron responses can obscure what information these areas represent and how it is represented. Here we demonstrate the advantages of a new dimensionality reduction technique, demixed principal component analysis (dPCA), that decomposes population activity into a few components. In addition to systematically capturing the majority of the variance of the data, dPCA also exposes the dependence of the neural representation on task parameters such as stimuli, decisions, or rewards. To illustrate our method we reanalyze population data from four datasets comprising different species, different cortical areas and different experimental tasks. In each case, dPCA provides a concise way of visualizing the data that summarizes the task-dependent features of the population response in a single figure. [ABSTRACT FROM AUTHOR]

Lateral intraparietal (LIP) neurons represent formation of perceptual decisions involving eye movements. In circuit models for these decisions, neural ensembles that encode actions compete to form decisions. Consequently, representation and readout of the decision variables (DVs) are implemented similarly for decisions with identical competing actions, irrespective of input and task context differences. Further, DVs are encoded as partially potentiated action plans through balance of activity of action-selective ensembles. Here, we test those core principles. We show that in a novel face-discrimination task, LIP firing rates decrease with supporting evidence, contrary to conventional motion-discrimination tasks. These opposite response patterns arise from similar mechanisms in which decisions form along curved population-response manifolds misaligned with action representations. These manifolds rotate in state space based on context, indicating distinct optimal readouts for different tasks. We show similar manifolds in lateral and medial prefrontal cortices, suggesting similar representational geometry across decision-making circuits. [Display omitted] • We examine parietal neural activity in motion and face discrimination tasks • Population neural response dynamics form a curved manifold during decision-making • Manifolds rotates across tasks, changing optimal readout of the decision variable • Circuit models of perceptual decisions need revision to include task dependency Comparison of neuronal activity during decision-making in face and motion discrimination tasks reveals task-dependent response geometry that shapes optimal readout of the decision variable. [ABSTRACT FROM AUTHOR]