4 research outputs found

    Differential influences of environment and self-motion on place and grid cell firing

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    Place and grid cells in the hippocampal formation provide foundational representations of environmental location, and potentially of locations within conceptual spaces. Some accounts predict that environmental sensory information and self-motion are encoded in complementary representations, while other models suggest that both features combine to produce a single coherent representation. Here, we use virtual reality to dissociate visual environmental from physical motion inputs, while recording place and grid cells in mice navigating virtual open arenas. Place cell firing patterns predominantly reflect visual inputs, while grid cell activity reflects a greater influence of physical motion. Thus, even when recorded simultaneously, place and grid cell firing patterns differentially reflect environmental information (or ‘states’) and physical self-motion (or ‘transitions’), and need not be mutually coherent

    Computational Models of Grid Cell Firing

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    International audienceOverview Grid cells in the medial entorhinal cortex (mEC) fire whenever the animal enters a regular triangular array of locations that cover its environment. Since their discovery, several models that can account for these remarkably regular spatial firing patterns have been proposed. These generally fall into one of three classes, generating grid cell firing patterns either by oscillatory interference, through continuous attractor dynamics, or as a result of spatially modulated input from a place cell population. Neural network simulations have been used to explore the implications and predictions made by each class of model, while subsequent experimental data have allowed their architecture to be refined. Here, we describe implementations of two classes of grid cell model-oscillatory interference and continuous attractor dynamics-alongside a hybrid model that incorporates the principal features of each. These models are intended to be both parsimonious and make testable predictions. We discuss the strengths and weaknesses of each model and the predictions they make for future experimental manipulations of the grid cell network in vivo

    A single-cell spiking model for the origin of grid-cell patterns

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