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Chklovskii, D. B.

Publications and source records attributed to Chklovskii, D. B..

9 recordsLinked to original sources

Correcting Non-Uniform Milling in FIB-SEM Images with Unsupervised Cross-Plane Image-to-Image Translation

MotivationFocused Ion Beam Scanning Electron Microscopy (FIB-SEM) is an advanced Volume Electron Microscopy technology with growing applications, featuring thinner sectioning compared to other Volume Electron Microscopes. Such axial resolution is crucial for accurate segmentation and reconstruction of fine structures in biological tissues. However, in reality, the milling thickness is not always uniform across the sample surface, resulting in the axial plane looking distorted. Existing image processing approaches often: (i) assume constant section thickness; (ii) consist of multiple separate processing steps (i.e., not in an end-to-end fashion); (iii) require ground truth images for modeling, which may entail significant labor and be unsuitable for rapid analysis. ResultsWe develop a deep learning method to correct non-uniform milling artifacts observed in FIB-SEM images. The proposed method is an image-to-image translation technique that can mitigate image distortions in an unsupervised manner. It conducts cross-plane learning within 3D image volumes without any ground truth annotations. We demonstrate the efficacy of our method on a real-world micro-wasp dataset, showcasing significantly improved image quality after correction with qualitative and quantitative analysis. Contactpfister@seas.harvard.edu, jingpengw@lglab.ac.cn

bioinformatics↗

The first complete 3D reconstruction and morphofunctional mapping of an insect eye

The structure of compound eyes in arthropods has been the subject of many studies, revealing important biological principles. Until recently, these studies were constrained by the two-dimensional nature of available ultrastructural data. By taking advantage of the novel three-dimensional ultrastructural dataset obtained using volume electron microscopy (vEM), we present the first cellular-level reconstruction of the whole compound eye of an insect, the miniaturized parasitoid wasp Megaphragma viggianii. The compound eye of the female M. viggianii consists of 29 ommatidia and contains 478 cells. Despite the almost anucleate brain, all cells of the compound eye contain nuclei. As in larger insects, the dorsal rim area (DRA) of the eye in M. viggianii contains ommatidia that are believed to be specialized in polarized light detection as reflected in their corneal and retinal morphology. We report the presence of three ectopic photoreceptors. Our results offer new insights into the miniaturization of compound eyes and scaling of sensory organs in general.

zoology↗

The Neuron as a Direct Data-Driven Controller

In the quest to model neuronal function amidst gaps in physiological data, a promising strategy is to develop a normative theory that interprets neuronal physiology as optimizing a computational objective. This study extends the current normative models, which primarily optimize prediction, by conceptualizing neurons as optimal feedback controllers. We posit that neurons, especially those beyond early sensory areas, act as controllers, steering their environment towards a specific desired state through their output. This environment comprises both synaptically interlinked neurons and external motor sensory feedback loops, enabling neurons to evaluate the effectiveness of their control via synaptic feedback. Utilizing the novel Direct Data-Driven Control (DD-DC) framework, we model neurons as biologically feasible controllers which implicitly identify loop dynamics, infer latent states and optimize control. Our DD-DC neuron model explains various neurophysiological phenomena: the shift from potentiation to depression in Spike-Timing-Dependent Plasticity (STDP) with its asymmetry, the duration and adaptive nature of feedforward and feedback neuronal filters, the imprecision in spike generation under constant stimulation, and the characteristic operational variability and noise in the brain. Our model presents a significant departure from the traditional, feedforward, instant-response McCulloch-Pitts-Rosenblatt neuron, offering a novel and biologically-informed fundamental unit for constructing neural networks.

neuroscience↗

A linear discriminant analysis model of imbalanced associative learning in the mushroom body compartment

To adapt to their environments, animals learn associations between sensory stimuli and unconditioned stimuli. In invertebrates, olfactory associative learning primarily occurs in the mushroom body, which is segregated into separate compartments. Within each compartment, Kenyon cells (KCs) encoding sparse odor representations project onto mushroom body output neurons (MBONs) whose outputs guide behavior. Associated with each compartment is a dopamine neuron (DAN) that modulates plasticity of the KC-MBON synapses within the compartment. Interestingly, DAN-induced plasticity of the KC-MBON synapse is imbalanced in the sense that it only weakens the synapse and is temporally sparse. We propose a normative mechanistic model of the MBON as a linear discriminant analysis (LDA) classifier that predicts the presence of an unconditioned stimulus (class identity) given a KC odor representation (feature vector). Starting from a principled LDA objective function and under the assumption of temporally sparse DAN activity, we derive an online algorithm which maps onto the mushroom body compartment. Our model accounts for the imbalanced learning at the KC-MBON synapse and makes testable predictions that provide clear contrasts with existing models.

neuroscience↗

Normative and mechanistic model of an adaptive circuit for efficient encoding and feature extraction

One major question in neuroscience is how to relate connectomes to neural activity, circuit function, and learning. We offer an answer in the peripheral olfactory circuit of the Drosophila larva, composed of olfactory receptor neurons (ORNs) connected through feedback loops with interconnected inhibitory local neurons (LNs). We combine structural and activity data and, using a holistic normative framework based on similarity-matching, we propose a biologically plausible mechanistic model of the circuit. Our model predicts the ORN [->] LN synaptic weights found in the connectome and demonstrate that they reflect correlations in ORN activity patterns. Additionally, our model explains the relation between ORN [->] LN and LN - LN synaptic weight and the arising of different LN types. This global synaptic organization can autonomously arise through Hebbian plasticity, and thus allows the circuit to adapt to different environments in an unsupervised manner. Functionally, we propose LNs extract redundant input correlations and dampen them in ORNs, thus partially whitening and normalizing the stimulus representations in ORNs. Our work proposes a comprehensive framework to combine structure, activity, function, and learning, and uncovers a general and potent circuit motif that can learn and extract significant input features and render stimulus representations more efficient. SignificanceThe brain represents information with patterns of neural activity. At the periphery, due to the properties of the external world and of encoding neurons, these patterns contain correlations, which are detrimental for stimulus discrimination. We study the peripheral olfactory neural circuit of the Drosophila larva, that preprocesses neural representations before relaying them to higher brain areas. A comprehensive understanding of this preprocessing is, however, lacking. Here, we propose a mechanistic and normative framework describing the function of the circuit and predict the circuits synaptic organization based on the circuits input neural activity. We show how the circuit can autonomously adapt to different environments, extracts stimulus features, and decorrelate and normalize input representations, which facilitates odor discrimination downstream.

neuroscience↗

Coordinated drift of receptive fields during noisy representation learning

Long-term memories and learned behavior are conventionally associated with stable neuronal representations. However, recent experiments showed that neural population codes in many brain areas continuously change even when animals have fully learned and stably perform their tasks. This representational "drift" naturally leads to questions about its causes, dynamics, and functions. Here, we explore the hypothesis that neural representations optimize a representational objective with a degenerate solution space, and noisy synaptic updates drive the network to explore this (near-)optimal space causing representational drift. We illustrate this idea in simple, biologically plausible Hebbian/anti-Hebbian network models of representation learning, which optimize similarity matching objectives, and, when neural outputs are constrained to be nonnegative, learn localized receptive fields (RFs) that tile the stimulus manifold. We find that the drifting RFs of individual neurons can be characterized by a coordinated random walk, with the effective diffusion constants depending on various parameters such as learning rate, noise amplitude, and input statistics. Despite such drift, the representational similarity of population codes is stable over time. Our model recapitulates recent experimental observations in hippocampus and posterior parietal cortex, and makes testable predictions that can be probed in future experiments.

neuroscience↗

Neural circuits for dynamics-based segmentation of time series

The brain must extract behaviorally relevant latent variables from the signals streamed by the sensory organs. Such latent variables are often encoded in the dynamics that generated the signal rather than in the specific realization of the waveform. Therefore, one problem faced by the brain is to segment time series based on underlying dynamics. We present two algorithms for performing this segmentation task that are biologically plausible, which we define as acting in a streaming setting and all learning rules being local. One algorithm is model-based and can be derived from an optimization problem involving a mixture of autoregressive processes. This algorithm relies on feedback in the form of a prediction error, and can also be used for forecasting future samples. In some brain regions, such as the retina, the feedback connections necessary to use the prediction error for learning are absent. For this case, we propose a second, model-free algorithm that uses a running estimate of the autocorrelation structure of the signal to perform the segmentation. We show that both algorithms do well when tasked with segmenting signals drawn from autoregressive models with piecewise-constant parameters. In particular, the segmentation accuracy is similar to that obtained from oracle-like methods in which the ground-truth parameters of the autoregressive models are known. We also test our methods on datasets generated by alternating snippets of voice recordings. We provide implementations of our algorithms at https://github.com/ttesileanu/bio-time-series.

neuroscience↗

CaImAn: An open source tool for scalable Calcium Imaging data Analysis

Advances in fluorescence microscopy enable monitoring larger brain areas in-vivo with finer time resolution. The resulting data rates require reproducible analysis pipelines that are reliable, fully automated, and scalable to datasets generated over the course of months. Here we present CaImAn, an open-source library for calcium imaging data analysis. CaImAn provides automatic and scalable methods to address problems common to pre-processing, including motion correction, neural activity identification, and registration across different sessions of data collection. It does this while requiring minimal user intervention, with good performance on computers ranging from laptops to high-performance computing clusters. CaImAn is suitable for two-photon and one-photon imaging, and also enables real-time analysis on streaming data. To benchmark the performance of CaImAn we collected a corpus of ground truth annotations from multiple labelers on nine mouse two-photon datasets. We demonstrate that CaImAn achieves near-human performance in detecting locations of active neurons.

neuroscience↗

A clustering neural network model of insect olfaction

A key step in insect olfaction is the transformation of a dense representation of odors in a small population of neurons - projection neurons (PNs) of the antennal lobe - into a sparse representation in a much larger population of neurons - Kenyon cells (KCs) of the mushroom body. What computational purpose does this transformation serve? We propose that the PN-KC network implements an online clustering algorithm which we derive from the k-means cost function. The vector of PN-KC synaptic weights converging onto a given KC represents the corresponding cluster centroid. KC activities represent attribution indices, i.e. the degree to which a given odor presentation is attributed to each cluster. Remarkably, such clustering view of the PN-KC circuit naturally accounts for several of its salient features. First, attribution indices are nonnegative thus rationalizing rectification in KCs. Second, the constraint on the total sum of attribution indices for each presentation is enforced by a Lagrange multiplier identified with the activity of a single inhibitory interneuron reciprocally connected with KCs. Third, the soft-clustering version of our algorithm reproduces observed sparsity and overcompleteness of the KC representation which may optimize supervised classification downstream.

neuroscience↗