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      Neural Population Dynamics during Reaching Are Better Explained by a Dynamical System than Representational Tuning

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          Abstract

          Recent models of movement generation in motor cortex have sought to explain neural activity not as a function of movement parameters, known as representational models, but as a dynamical system acting at the level of the population. Despite evidence supporting this framework, the evaluation of representational models and their integration with dynamical systems is incomplete in the literature. Using a representational velocity-tuning based simulation of center-out reaching, we show that incorporating variable latency offsets between neural activity and kinematics is sufficient to generate rotational dynamics at the level of neural populations, a phenomenon observed in motor cortex. However, we developed a covariance-matched permutation test (CMPT) that reassigns neural data between task conditions independently for each neuron while maintaining overall neuron-to-neuron relationships, revealing that rotations based on the representational model did not uniquely depend on the underlying condition structure. In contrast, rotations based on either a dynamical model or motor cortex data depend on this relationship, providing evidence that the dynamical model more readily explains motor cortex activity. Importantly, implementing a recurrent neural network we demonstrate that both representational tuning properties and rotational dynamics emerge, providing evidence that a dynamical system can reproduce previous findings of representational tuning. Finally, using motor cortex data in combination with the CMPT, we show that results based on small numbers of neurons or conditions should be interpreted cautiously, potentially informing future experimental design. Together, our findings reinforce the view that representational models lack the explanatory power to describe complex aspects of single neuron and population level activity.

          Author Summary

          The question of how the brain generates movement has been extensively studied, yet multiple competing models exist. Representational approaches relate the activity of single neurons to movement parameters such as velocity and position, approaches useful for the decoding of movement intentions, while the dynamical systems approach predicts that neural activity should evolve in a predictable way based on population activity. Existing representational models cannot reproduce the recent finding in monkeys that predictable rotational patterns underlie motor cortex activity during reach initiation, a finding predicted by a dynamical model in which muscle activity is a direct combination of neural population rotations. However, previous simulations did not consider an essential aspect of representational models: variable time offsets between neurons and kinematics. Whereas these offsets reveal rotational patterns in the model, these rotations are statistically different from those observed in the brain and predicted by a dynamical model. Importantly, a simple recurrent neural network model also showed rotational patterns statistically similar to those observed in the brain, supporting the idea that dynamical systems-based approaches may provide a powerful explanation of motor cortex function.

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          Most cited references36

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          Neural population dynamics during reaching

          Most theories of motor cortex have assumed that neural activity represents movement parameters. This view derives from an analogous approach to primary visual cortex, where neural activity represents patterns of light. Yet it is unclear how well that analogy holds. Single-neuron responses in motor cortex appear strikingly complex, and there is marked disagreement regarding which movement parameters are represented. A better analogy might be with other motor systems, where a common principle is rhythmic neural activity. We found that motor cortex responses during reaching contain a brief but strong oscillatory component, something quite unexpected for a non-periodic behavior. Oscillation amplitude and phase followed naturally from the preparatory state, suggesting a mechanistic role for preparatory neural activity. These results demonstrate unexpected yet surprisingly simple structure in the population response. That underlying structure explains many of the confusing features of individual-neuron responses.
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            Generating coherent patterns of activity from chaotic neural networks.

            Neural circuits display complex activity patterns both spontaneously and when responding to a stimulus or generating a motor output. How are these two forms of activity related? We develop a procedure called FORCE learning for modifying synaptic strengths either external to or within a model neural network to change chaotic spontaneous activity into a wide variety of desired activity patterns. FORCE learning works even though the networks we train are spontaneously chaotic and we leave feedback loops intact and unclamped during learning. Using this approach, we construct networks that produce a wide variety of complex output patterns, input-output transformations that require memory, multiple outputs that can be switched by control inputs, and motor patterns matching human motion capture data. Our results reproduce data on premovement activity in motor and premotor cortex, and suggest that synaptic plasticity may be a more rapid and powerful modulator of network activity than generally appreciated.
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              On the relations between the direction of two-dimensional arm movements and cell discharge in primate motor cortex.

              The activity of single cells in the motor cortex was recorded while monkeys made arm movements in eight directions (at 45 degrees intervals) in a two-dimensional apparatus. These movements started from the same point and were of the same amplitude. The activity of 606 cells related to proximal arm movements was examined in the task; 323 of the 606 cells were active in that task and were studied in detail. The frequency of discharge of 241 of the 323 cells (74.6%) varied in an orderly fashion with the direction of movement. Discharge was most intense with movements in a preferred direction and was reduced gradually when movements were made in directions farther and farther away from the preferred one. This resulted in a bell-shaped directional tuning curve. These relations were observed for cell discharge during the reaction time, the movement time, and the period that preceded the earliest changes in the electromyographic activity (approximately 80 msec before movement onset). In about 75% of the 241 directionally tuned cells, the frequency of discharge, D, was a sinusoidal function of the direction of movement, theta: D = b0 + b1 sin theta + b2cos theta, or, in terms of the preferred direction, theta 0: D = b0 + c1cos (theta - theta0), where b0, b1, b2, and c1 are regression coefficients. Preferred directions differed for different cells so that the tuning curves partially overlapped. The orderly variation of cell discharge with the direction of movement and the fact that cells related to only one of the eight directions of movement tested were rarely observed indicate that movements in a particular direction are not subserved by motor cortical cells uniquely related to that movement. It is suggested, instead, that a movement trajectory in a desired direction might be generated by the cooperation of cells with overlapping tuning curves. The nature of this hypothetical population code for movement direction remains to be elucidated.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Comput Biol
                PLoS Comput. Biol
                plos
                ploscomp
                PLoS Computational Biology
                Public Library of Science (San Francisco, CA USA )
                1553-734X
                1553-7358
                4 November 2016
                November 2016
                : 12
                : 11
                : e1005175
                Affiliations
                [1 ]German Primate Center, Göttingen, Germany
                [2 ]Faculty of Biology, Georg-August-Universität Göttingen, Göttingen, Germany
                Carnegie Mellon University, UNITED STATES
                Author notes

                The authors have declared that no competing interests exist.

                • Conceptualization: JAM BD HS.

                • Funding acquisition: HS.

                • Investigation: JAM BD.

                • Writing – original draft: JAM.

                • Writing – review & editing: JAM BD HS.

                Author information
                http://orcid.org/0000-0002-5179-3181
                http://orcid.org/0000-0001-6593-2800
                Article
                PCOMPBIOL-D-16-00345
                10.1371/journal.pcbi.1005175
                5096671
                27814352
                02a9e0bc-3322-4006-8429-c61785115b3f
                © 2016 Michaels et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 31 March 2016
                : 24 September 2016
                Page count
                Figures: 7, Tables: 0, Pages: 22
                Funding
                Funded by: funder-id http://dx.doi.org/10.13039/501100001659, Deutsche Forschungsgemeinschaft;
                Award ID: SCHE 1575/1-1 & 3-1
                Award Recipient :
                This work was supported by Deutsche Forschungsgemeinschaft (SCHE 1575/1-1 & SFB 889, Project C09). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Cell Biology
                Cellular Types
                Animal Cells
                Neurons
                Biology and Life Sciences
                Neuroscience
                Cellular Neuroscience
                Neurons
                Biology and Life Sciences
                Neuroscience
                Neuronal Tuning
                Computer and Information Sciences
                Systems Science
                Dynamical Systems
                Physical Sciences
                Mathematics
                Systems Science
                Dynamical Systems
                Physical Sciences
                Mathematics
                Discrete Mathematics
                Combinatorics
                Permutation
                Physical Sciences
                Mathematics
                Probability Theory
                Random Variables
                Covariance
                Biology and Life Sciences
                Anatomy
                Musculoskeletal System
                Medicine and Health Sciences
                Anatomy
                Musculoskeletal System
                Biology and Life Sciences
                Anatomy
                Brain
                Motor Cortex
                Medicine and Health Sciences
                Anatomy
                Brain
                Motor Cortex
                Computer and Information Sciences
                Neural Networks
                Biology and Life Sciences
                Neuroscience
                Neural Networks
                Custom metadata
                All relevant modeling data are within the paper and its supporting information files. We also compared our model with third party data (Churchland et al, 2012; http://doi.org/10.1038/nature11129) that was downloaded from: http://churchlandlab.neuroscience.columbia.edu/links.html. This data can be accessed there or by contacting the authors of the original study: Mark Churchland (email: mc3502@ 123456cumc.columbia.edu ); Krishna Shenoy (email: shenoy@ 123456stanford.edu ).

                Quantitative & Systems biology
                Quantitative & Systems biology

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