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      Representation of Non-Spatial and Spatial Information in the Lateral Entorhinal Cortex

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          Abstract

          Some theories of memory propose that the hippocampus integrates the individual items and events of experience within a contextual or spatial framework. The hippocampus receives cortical input from two major pathways: the medial entorhinal cortex (MEC) and the lateral entorhinal cortex (LEC). During exploration in an open field, the firing fields of MEC grid cells form a periodically repeating, triangular array. In contrast, LEC neurons show little spatial selectivity, and it has been proposed that the LEC may provide non-spatial input to the hippocampus. Here, we recorded MEC and LEC neurons while rats explored an open field that contained discrete objects. LEC cells fired selectively at locations relative to the objects, whereas MEC cells were weakly influenced by the objects. These results provide the first direct demonstration of a double dissociation between LEC and MEC inputs to the hippocampus under conditions of exploration typically used to study hippocampal place cells.

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          Most cited references56

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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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            Loss of recent memory after bilateral hippocampal lesions.

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              The medial temporal lobe.

              The medial temporal lobe includes a system of anatomically related structures that are essential for declarative memory (conscious memory for facts and events). The system consists of the hippocampal region (CA fields, dentate gyrus, and subicular complex) and the adjacent perirhinal, entorhinal, and parahippocampal cortices. Here, we review findings from humans, monkeys, and rodents that illuminate the function of these structures. Our analysis draws on studies of human memory impairment and animal models of memory impairment, as well as neurophysiological and neuroimaging data, to show that this system (a) is principally concerned with memory, (b) operates with neocortex to establish and maintain long-term memory, and (c) ultimately, through a process of consolidation, becomes independent of long-term memory, though questions remain about the role of perirhinal and parahippocampal cortices in this process and about spatial memory in rodents. Data from neurophysiology, neuroimaging, and neuroanatomy point to a division of labor within the medial temporal lobe. However, the available data do not support simple dichotomies between the functions of the hippocampus and the adjacent medial temporal cortex, such as associative versus nonassociative memory, episodic versus semantic memory, and recollection versus familiarity.
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                Author and article information

                Journal
                Front Behav Neurosci
                Front. Behav. Neurosci.
                Frontiers in Behavioral Neuroscience
                Frontiers Research Foundation
                1662-5153
                28 October 2011
                2011
                : 5
                : 69
                Affiliations
                [1] 1simpleKrieger Mind/Brain Institute, Johns Hopkins University Baltimore, MD, USA
                [2] 2simpleDepartment of Neurobiology and Anatomy, University of Texas Medical School at Houston Houston, TX, USA
                [3] 3simpleSolomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine Baltimore, MD, USA
                Author notes

                Edited by: Donald A. Wilson, New York University School of Medicine, USA

                Reviewed by: Rebecca D. Burwell, Brown University, USA; Anne-Marie Mouly, CNRS-Université de Lyon, UMR 5020, France

                *Correspondence: James J. Knierim, Krieger Mind/Brain Institute, Johns Hopkins University, 338 Krieger Hall, 3400 North Charles Street, Baltimore, MD 21218, USA. e-mail: jknierim@ 123456jhu.edu
                Article
                10.3389/fnbeh.2011.00069
                3203372
                22065409
                ee259770-747f-4819-9ce7-6222792ae27a
                Copyright © 2011 Deshmukh and Knierim.

                This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.

                History
                : 22 August 2011
                : 03 October 2011
                Page count
                Figures: 9, Tables: 1, Equations: 0, References: 63, Pages: 33, Words: 12160
                Categories
                Neuroscience
                Original Research

                Neurosciences
                memory,grid cells,medial entorhinal cortex,navigation,hippocampus,objects
                Neurosciences
                memory, grid cells, medial entorhinal cortex, navigation, hippocampus, objects

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