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Understanding a sensory system implies the ability to predict responses to a variety of inputs from a common model. In the retina, this includes predicting how the integration of signals across visual space shapes the outputs of retinal ganglion cells. Existing models of this process generalize poorly to predict responses to new stimuli. This failure arises in part from properties of the ganglion cell response that are not well captured by standard receptive-field mapping techniques: nonlinear spatial integration and fine-scale heterogeneities in spatial sampling. Here we characterize a ganglion cell's spatial receptive field using a mechanistic model based on measurements of the physiological properties and connectivity of only the primary excitatory circuitry of the retina. The resulting simplified circuit model successfully predicts ganglion-cell responses to a variety of spatial patterns and thus provides a direct correspondence between circuit connectivity and retinal output.
Models, Anatomic, Neurons, Retinal Ganglion Cells, Retinal Bipolar Cells, Patch-Clamp Techniques, Time Factors, Models, Neurological, Action Potentials, Membrane Proteins, In Vitro Techniques, Transfection, Article, Retina, Luminescent Proteins, Mice, Nonlinear Dynamics, Animals, Visual Fields, Disks Large Homolog 4 Protein, Guanylate Kinases, Photic Stimulation
Models, Anatomic, Neurons, Retinal Ganglion Cells, Retinal Bipolar Cells, Patch-Clamp Techniques, Time Factors, Models, Neurological, Action Potentials, Membrane Proteins, In Vitro Techniques, Transfection, Article, Retina, Luminescent Proteins, Mice, Nonlinear Dynamics, Animals, Visual Fields, Disks Large Homolog 4 Protein, Guanylate Kinases, Photic Stimulation
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 193 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 1% | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 1% |