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      Coherence among Head Direction Cells before Eye Opening in Rat Pups

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          Summary

          Mammalian navigation is thought to depend on an internal map of space consisting of functionally specialized cells in the hippocampus and the surrounding parahippocampal cortices [ 1–7]. Basic properties of this map are present when rat pups explore the world outside of their nest for the first time, around postnatal day 16–18 (P16–P18) [ 8–10]. One of the first functions to be expressed in navigating animals is the directional tuning of the head direction cells [ 8, 9]. To determine whether head direction tuning is expressed at even earlier ages, before the start of exploration, and to establish whether vision is necessary for the development of directional tuning, we recorded neural activity in pre- and parasubiculum, or medial entorhinal cortex, from P11 onward, 3–4 days before the eyelids unseal. Head direction cells were present from the first day of recording. Firing rates were lower than in adults, and preferred firing directions were less stable, drifting within trials and changing completely between trials. Yet the cells drifted coherently, i.e., relative firing directions were maintained from one trial to the next. Directional tuning stabilized shortly after eye opening. The data point to a hardwired attractor network for representation of head direction in which directional tuning develops before vision and visual input serves primarily to anchor firing direction to the external world.

          Highlights

          • Head direction cells are present 3–4 days before eye opening or earlier

          • Before eye opening, directional tuning is unstable

          • Head direction cells drift coherently before eye opening

          • Directional tuning stabilizes as soon as the eyes open

          Abstract

          Bjerknes et al. show that head direction cells are present in young rat pups several days before eye opening and initiation of active exploration. There is considerable drift in the cells’ directional preferences, but the relative differences in firing direction are maintained, consistent with a predominantly innate attractor network for directional representation.

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          Most cited references21

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          Microstructure of a spatial map in the entorhinal cortex.

          The ability to find one's way depends on neural algorithms that integrate information about place, distance and direction, but the implementation of these operations in cortical microcircuits is poorly understood. Here we show that the dorsocaudal medial entorhinal cortex (dMEC) contains a directionally oriented, topographically organized neural map of the spatial environment. Its key unit is the 'grid cell', which is activated whenever the animal's position coincides with any vertex of a regular grid of equilateral triangles spanning the surface of the environment. Grids of neighbouring cells share a common orientation and spacing, but their vertex locations (their phases) differ. The spacing and size of individual fields increase from dorsal to ventral dMEC. The map is anchored to external landmarks, but persists in their absence, suggesting that grid cells may be part of a generalized, path-integration-based map of the spatial environment.
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            The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat.

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              Representation of geometric borders in the entorhinal cortex.

              We report the existence of an entorhinal cell type that fires when an animal is close to the borders of the proximal environment. The orientation-specific edge-apposing activity of these "border cells" is maintained when the environment is stretched and during testing in enclosures of different size and shape in different rooms. Border cells are relatively sparse, making up less than 10% of the local cell population, but can be found in all layers of the medial entorhinal cortex as well as the adjacent parasubiculum, often intermingled with head-direction cells and grid cells. Border cells may be instrumental in planning trajectories and anchoring grid fields and place fields to a geometric reference frame.
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                Author and article information

                Contributors
                Journal
                Curr Biol
                Curr. Biol
                Current Biology
                Cell Press
                0960-9822
                1879-0445
                05 January 2015
                05 January 2015
                : 25
                : 1
                : 103-108
                Affiliations
                [1 ]Kavli Institute for Systems Neuroscience, Norwegian University of Science and Technology, 7489 Trondheim, Norway
                [2 ]Division of Neuroscience, Medical Research Institute, University of Dundee, Ninewells Hospital and Medical School, Dundee DD1 9SY, Scotland, UK
                Author notes
                []Corresponding author maybm@ 123456ntnu.no
                Article
                S0960-9822(14)01436-5
                10.1016/j.cub.2014.11.009
                4291142
                25466682
                89e0fc0e-cd45-4368-8b7e-c7971b9832db
                © 2015 The Authors. Published by Elsevier Ltd.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).

                History
                : 14 October 2014
                : 5 November 2014
                : 5 November 2014
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                Life sciences
                Life sciences

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