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      Laminar Localization and Projection-Specific Properties of Presubicular Neurons Targeting the Lateral Mammillary Nucleus, Thalamus, or Medial Entorhinal Cortex

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          The presubiculum (PrS) is part of an interconnected network of distributed brain regions where individual neurons signal the animals heading direction. PrS sends axons to medial entorhinal cortex (MEC), it is reciprocally connected with anterior thalamic nuclei (ATNs), and it sends feedback projections to the lateral mammillary nucleus (LMN), involved in generating the head direction signal. The intrinsic properties of projecting neurons will influence the pathway-specific transmission of activity. Here, we used projection-specific labeling of presubicular neurons to identify MEC-, LMN-, and ATN-projecting neurons in mice. MEC-projecting neurons located in superficial layers II/III were mostly regular spiking pyramidal neurons, and we also identified a Martinotti-type GABAergic neuron. The cell bodies of LMN-projecting neurons were located in a well-delimited area in the middle portion of the PrS, which corresponds to layer IV. The physiology of LMN projecting, pyramidal neurons stood out with a tendency to fire in bursts of action potentials (APs) with rapid onset. These properties may be uniquely adapted to reliably transmit visual landmark information with short latency to upstream LMN. Neurons projecting to ATN were located in layers V/VI, and they were mostly regular spiking pyramidal neurons. Unsupervised cluster analysis of intrinsic properties suggested distinct physiological features for the different categories of projection neurons, with some similarities between MEC- and ATN-projecting neurons. Projection-specific subpopulations may serve separate functions in the PrS and may be engaged differently in transmitting head direction related information.

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          Most cited references40

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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 head direction signal: origins and sensory-motor integration.

            Navigation first requires accurate perception of one's spatial orientation within the environment, which consists of knowledge about location and directional heading. Cells within several limbic system areas of the mammalian brain discharge allocentrically as a function of the animal's directional heading, independent of the animal's location and ongoing behavior. These cells are referred to as head direction (HD) cells and are believed to encode the animal's perceived directional heading with respect to its environment. Although HD cells are found in several areas, the principal circuit for generating this signal originates in the dorsal tegmental nucleus and projects serially, with some reciprocal connections, to the lateral mammillary nucleus --> anterodorsal thalamus --> PoS, and terminates in the entorhinal cortex. HD cells receive multimodal information about landmarks and self-generated movements. Vestibular information appears critical for generating the directional signal, but motor/proprioceptive and landmark information are important for updating it.
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              Intrinsic firing patterns of diverse neocortical neurons.

              Neurons of the neocortex differ dramatically in the patterns of action potentials they generate in response to current steps. Regular-spiking cells adapt strongly during maintained stimuli, whereas fast-spiking cells can sustain very high firing frequencies with little or no adaptation. Intrinsically bursting cells generate clusters of spikes (bursts), either singly or repetitively. These physiological distinctions have morphological correlates. RS and IB cells can be either pyramidal neurons or spiny stellate cells, and thus constitute the excitatory cells of the cortex. FS cells are smooth or sparsely spiny non-pyramidal cells, and are likely to be GABAergic inhibitory interneurons. The different firing properties of neurons in neocortex contribute significantly to its network behavior.
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                Author and article information

                Journal
                eNeuro
                eNeuro
                eneuro
                eneuro
                eNeuro
                eNeuro
                Society for Neuroscience
                2373-2822
                28 April 2017
                15 May 2017
                Mar-Apr 2017
                : 4
                : 2
                : ENEURO.0370-16.2017
                Affiliations
                [1 ]Inserm U1127, CNRS UMR7225, UPMC Université Paris 6 UMR S1127, Institut du Cerveau et de la Moelle Epinière, Sorbonne Universités , Paris 75013, France
                [2 ]CNRS UMR 8119, Université Paris Descartes , France
                Author notes

                The authors declare no competing financial interests.

                Author contributions: J.S. and D.F. designed research; L.-W.H., J.S., M.N., and R.L. performed research; L.-W.H., L.R., and D.F. analyzed data; L.-W.H., J.S., and D.F. wrote the paper.

                This work was supported by the ANR-10-JCJC-1406 (to D.F.) and the Centre National des Etudes Spatiales (to L.R.).

                [*]

                L.-W.H. and J.S. contributed equally to this work.

                Correspondence should be addressed to either of the following: Desdemona Fricker, M.D., Ph.D., CNRS UMR8119 Université Paris Descartes, 45 Rue des Saints-Pères, 75006 Paris, France, E-mail: desdemona.fricker@ 123456parisdescartes.fr ; or Jean Simonnet, Ph.D., Bernstein Center for Computational Neuroscience, Humboldt University Berlin, 10115 Berlin, Germany, E-mail: jean.simonnet@ 123456bccn-berlin.de .
                Author information
                http://orcid.org/0000-0002-2438-5940
                http://orcid.org/0000-0003-3763-7614
                http://orcid.org/0000-0001-7328-9480
                Article
                eN-NWR-0370-16
                10.1523/ENEURO.0370-16.2017
                5430300
                28508034
                c718e4d8-9c4c-48bc-a782-98858e3256e1
                Copyright © 2017 Huang et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 14 December 2016
                : 19 April 2017
                : 24 April 2017
                Page count
                Figures: 5, Tables: 3, Equations: 0, References: 43, Pages: 0, Words: 7787
                Funding
                Funded by: Agence Nationale de la Recherche (ANR)
                Award ID: 501100001665
                Award ID: ANR-10-JCJC-1406
                Categories
                5
                5.1
                New Research
                Integrative Systems
                Custom metadata
                March/April 2017

                cell morphology,electrical properties,head direction,patch clamp,postsubiculum,retrograde tracing

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