2013
DOI: 10.1126/science.1232627
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Optogenetic Dissection of Entorhinal-Hippocampal Functional Connectivity

Abstract: We used a combined optogenetic-electrophysiological strategy to determine the functional identity of entorhinal cells with output to the place-cell population in the hippocampus. Channelrhodopsin-2 (ChR2) was expressed selectively in the hippocampus-targeting subset of entorhinal projection neurons by infusing retrogradely transportable ChR2-coding recombinant adeno-associated virus in the hippocampus. Virally transduced ChR2-expressing cells were identified in medial entorhinal cortex as cells that fired at f… Show more

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Cited by 240 publications
(296 citation statements)
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References 62 publications
(89 reference statements)
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“…In these studies, the majority of layer II grid cells had stellatespecific morphological and electrophysiological properties. The suggestion that many grid cells are stellate cells is consistent with the fact that (i) stellate cells are the main origin of the layer II projections to dentate gyrus and CA3 149,150 , and (ii) grid cells are abundant among hippocampus-projecting MEC neurons 146,151 . Yet these observations do not rule out that some grid cells are pyramidal cells.…”
Section: Uniqueness Of the Entorhinal Grid Networksupporting
confidence: 57%
“…In these studies, the majority of layer II grid cells had stellatespecific morphological and electrophysiological properties. The suggestion that many grid cells are stellate cells is consistent with the fact that (i) stellate cells are the main origin of the layer II projections to dentate gyrus and CA3 149,150 , and (ii) grid cells are abundant among hippocampus-projecting MEC neurons 146,151 . Yet these observations do not rule out that some grid cells are pyramidal cells.…”
Section: Uniqueness Of the Entorhinal Grid Networksupporting
confidence: 57%
“…Alternatively, place cells may be generated from other classes of spatially modulated cells, such as border cells, which have adult-like properties from the very first day of exploration outside the nest (Bjerknes et al 2014). Retrograde labeling studies suggest that border cells have projections to the hippocampus that may be equally dense as those from grid cells, although the latter are more abundant (Zhang et al 2013). A potential role for border cells in place-cell formation would be consistent with early models, suggesting that place cells arise by linear combination of inputs from cells with firing fields defined by their proximity to geometric boundaries (O'Keefe and Burgess 1996;Hartley et al 2000).…”
Section: Upstream Of Place Cells: Grid Cells and Other Cell Typessupporting
confidence: 56%
“…A potential role for border cells in place-cell formation would be consistent with early models, suggesting that place cells arise by linear combination of inputs from cells with firing fields defined by their proximity to geometric boundaries (O'Keefe and Burgess 1996;Hartley et al 2000). Recordings in the medial entorhinal cortex have, so far, identified such cells only near the boundaries of the environment Zhang et al 2013;Bjerknes et al 2014), suggesting that a contriPlace Cells, Grid Cells, and Memory 2015;7:a021808 bution by these cells may be limited to place cells with peripheral firing fields.…”
Section: Upstream Of Place Cells: Grid Cells and Other Cell Typessupporting
confidence: 54%
“…In addition to its extensive cortical connectivity, the claustrum is densely interconnected with an array of subcortical structures (Figure 2), for example, thalamus (Figure 3; Herkenham, 1978;McKenna and Vertes, 2004;Vertes et al, 2006;Vertes and Hoover, 2008), striatum (Andersen, 1968;Wang et al, 2017), hippocampus (Amaral and Cowan, 1980;Zhang et al, 2013), amygdala (Majak et al, 2002;Wang et al, 2017) and hypothalamus (Vertes, 1992). Of its thalamic interactions, claustro-reuniens and claustro-rhomboid connectivity is particularly striking (Figure 3; Herkenham, 1978;McKenna and Vertes, 2004;Vertes et al, 2006).…”
Section: Subcortical Connectivitymentioning
confidence: 99%