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Willats, A. A.

Publications and source records attributed to Willats, A. A..

2 recordsLinked to original sources

Learning sparse codes from compressed representations with biologically plausible local wiring constraints

Sparse coding is an important method for unsupervised learning of task-independent features in theoretical neuroscience models of neural coding. While a number of algorithms exist to learn these representations from the statistics of a dataset, they largely ignore the information bottlenecks present in fiber pathways connecting cortical areas. For example, the visual pathway has many fewer neurons transmitting visual information to cortex than the number of photoreceptors. Both empirical and analytic results have recently shown that sparse representations can be learned effectively after performing dimensionality reduction with randomized linear operators, producing latent coefficients that preserve information. Unfortunately, current proposals for sparse coding in the compressed space require a centralized compression process (i.e., dense random matrix) that is biologically unrealistic due to local wiring constraints observed in neural circuits. The main contribution of this paper is to leverage recent results on structured random matrices to propose a theoretical neuroscience model of randomized projections for communication between cortical areas that is consistent with the local wiring constraints observed in neuroanatomy. We show analytically and empirically that unsupervised learning of sparse representations can be performed in the compressed space despite significant local wiring constraints in compression matrices of varying forms (corresponding to different local wiring patterns). Our analysis verifies that even with significant local wiring constraints, the learned representations remain qualitatively similar, have similar quantitative performance in both training and generalization error, and are consistent across many measures with measured macaque V1 receptive fields.

neuroscience

State-space optimal feedback control of optogenetically driven neural activity

ObjectiveThe rapid acceleration of tools for recording neuronal populations and targeted optogenetic manipulation has enabled real-time, feedback control of neuronal circuits in the brain. Continuously-graded control of measured neuronal activity poses a wide range of technical challenges, which we address through a combination of optogenetic stimulation and a state-space optimal control framework implemented in the thalamocortical circuit of the awake mouse. ApproachClosed-loop optogenetic control of neurons was performed in real-time via stimulation of channelrhodopsin-2 expressed in the somatosensory thalamus of the head-fixed mouse. A state-space linear dynamical system model structure was used to approximate the light-to-spiking input-output relationship in both single-neuron as well as multi-neuron scenarios when recording from multielectrode arrays. These models were utilized to design state feedback controller gains by way of linear quadratic optimal control and were also used online for estimation of state feedback, where a parameter-adaptive Kalman filter provided robustness to model-mismatch Main resultsThis model-based control scheme proved effective for feedback control of single-neuron firing rate in the thalamus of awake animals. Notably, the graded optical actuation utilized here did not synchronize simultaneously recorded neurons, but heterogeneity across the neuronal population resulted in a varied response to stimulation. Simulated multi-output feedback control provided better control of a heterogeneous population and demonstrated how the approach generalizes beyond single-neuron applications SignificanceTo our knowledge, this work represents the first experimental application of state space model-based feedback control for optogenetic stimulation. In combination with linear quadratic optimal control, the approaches here should generalize to future problems involving the control of highly complex neural circuits. More generally, feedback control of neuronal circuits opens the door to adaptively interacting with the dynamics underlying sensory, motor, and cognitive signaling, enabling a deeper understanding of circuit function and ultimately the control of function in injury or disease.

neuroscience