Impact of temporal coding of presynaptic entorhinal cortex grid cells on the formation of hippocampal place fields

2008 ◽  
Vol 21 (2-3) ◽  
pp. 303-310 ◽  
Author(s):  
Colin Molter ◽  
Yoko Yamaguchi
Keyword(s):  
Entorhinal Cortex ◽  
Temporal Coding ◽  
Grid Cells ◽  
Place Fields

scholarly journals A geometric attractor mechanism for self-organization of entorhinal grid modules

eLife ◽  
2019 ◽  
Vol 8 ◽  
Author(s):  
Louis Kang ◽  
Vijay Balasubramanian
Keyword(s):  
Entorhinal Cortex ◽  
Network Models ◽  
Recurrent Inhibition ◽  
Modular Structure ◽  
Self Organization ◽  
Periodic Lattice ◽  
Grid Cells ◽  
Medial Entorhinal Cortex ◽  
Attractor Network ◽  
Discrete Values

Grid cells in the medial entorhinal cortex (MEC) respond when an animal occupies a periodic lattice of ‘grid fields’ in the environment. The grids are organized in modules with spatial periods, or scales, clustered around discrete values separated on average by ratios in the range 1.4–1.7. We propose a mechanism that produces this modular structure through dynamical self-organization in the MEC. In attractor network models of grid formation, the grid scale of a single module is set by the distance of recurrent inhibition between neurons. We show that the MEC forms a hierarchy of discrete modules if a smooth increase in inhibition distance along its dorso-ventral axis is accompanied by excitatory interactions along this axis. Moreover, constant scale ratios between successive modules arise through geometric relationships between triangular grids and have values that fall within the observed range. We discuss how interactions required by our model might be tested experimentally.

scholarly journals Shedding light on stellate cells

eLife ◽  
2018 ◽  
Vol 7 ◽  
Author(s):  
Andrew S Alexander ◽  
Michael E Hasselmo
Keyword(s):  
Entorhinal Cortex ◽  
Stellate Cells ◽  
Grid Cells ◽  
Medial Entorhinal Cortex ◽  
The Relationship

The relationship between grid cells and two types of neurons found in the medial entorhinal cortex has been clarified.

scholarly journals Functional connectivity of the entorhinal–hippocampal space circuit

2014 ◽  
Vol 369 (1635) ◽  
pp. 20120516 ◽  
Author(s):  
Sheng-Jia Zhang ◽  
Jing Ye ◽  
Jonathan J. Couey ◽  
Menno Witter ◽  
Edvard I. Moser ◽  
...  
Keyword(s):  
Entorhinal Cortex ◽  
Cell Types ◽  
Place Cells ◽  
Projection Neurons ◽  
Border Cells ◽  
Head Direction ◽  
Grid Cells ◽  
Head Direction Cells ◽  
Dynamic Interactions ◽  
Cell Groups

The mammalian space circuit is known to contain several functionally specialized cell types, such as place cells in the hippocampus and grid cells, head-direction cells and border cells in the medial entorhinal cortex (MEC). The interaction between the entorhinal and hippocampal spatial representations is poorly understood, however. We have developed an optogenetic strategy to identify functionally defined cell types in the MEC that project directly to the hippocampus. By expressing channelrhodopsin-2 (ChR2) selectively in the hippocampus-projecting subset of entorhinal projection neurons, we were able to use light-evoked discharge as an instrument to determine whether specific entorhinal cell groups—such as grid cells, border cells and head-direction cells—have direct hippocampal projections. Photoinduced firing was observed at fixed minimal latencies in all functional cell categories, with grid cells as the most abundant hippocampus-projecting spatial cell type. We discuss how photoexcitation experiments can be used to distinguish the subset of hippocampus-projecting entorhinal neurons from neurons that are activated indirectly through the network. The functional breadth of entorhinal input implied by this analysis opens up the potential for rich dynamic interactions between place cells in the hippocampus and different functional cell types in the entorhinal cortex (EC).

scholarly journals Dynamic self-organized error-correction of grid cells by border cells

2018 ◽  
Author(s):  
Eli Pollock ◽  
Niral Desai ◽  
Xue-xin Wei ◽  
Vijay Balasubramanian
Keyword(s):  
Error Correction ◽  
Entorhinal Cortex ◽  
Path Integration ◽  
Network Models ◽  
Cell Types ◽  
Border Cells ◽  
Grid Cells ◽  
Spatially Correlated ◽  
Self Organized ◽  
Hebbian Plasticity

Grid cells in the entorhinal cortex are believed to establish their regular, spatially correlated firing patterns by path integration of the animal’s motion. Mechanisms for path integration, e.g. in attractor network models, predict stochastic drift of grid responses, which is not observed experimentally. We demonstrate a biologically plausible mechanism of dynamic self-organization by which border cells, which fire at environmental boundaries, can correct such drift in grid cells. In our model, experience-dependent Hebbian plasticity during exploration allows border cells to learn connectivity to grid cells. Border cells in this learned network reset the phase of drifting grids. This error-correction mechanism is robust to environmental shape and complexity, including enclosures with interior barriers, and makes distinctive predictions for environmental deformation experiments. Our work demonstrates how diverse cell types in the entorhinal cortex could interact dynamically and adaptively to achieve robust path integration.

scholarly journals Spike afterpotentials shape the in-vivo burst activity of principal cells in medial entorhinal cortex

2019 ◽  
Author(s):  
Dóra É. Csordás ◽  
Caroline Fischer ◽  
Johannes Nagele ◽  
Martin Stemmler ◽  
Andreas V.M. Herz
Keyword(s):  
Entorhinal Cortex ◽  
High Frequency ◽  
Cell Group ◽  
Two Dimensional ◽  
Grid Cells ◽  
Spatial Coding ◽  
Medial Entorhinal Cortex ◽  
Whole Cell

AbstractPrincipal neurons in rodent medial entorhinal cortex (MEC) generate high-frequency bursts during natural behavior. While in vitro studies point to potential mechanisms that could support such burst sequences, it remains unclear whether these mechanisms are effective under in-vivo conditions. In this study, we focused on the membrane-potential dynamics immediately following action potentials, as measured in whole-cell recordings from male mice running in virtual corridors (Domnisoru et al., 2013). These afterpotentials consisted either of a hyperpolarization, an extended ramp-like shoulder, or a depolarization reminiscent of depolarizing afterpotentials (DAPs) recorded in vitro in MEC stellate and pyramidal neurons. Next, we correlated the afterpotentials with the cells’ propensity to fire bursts. All DAP cells with known location resided in Layer II, generated bursts, and their inter-spike intervals (ISIs) were typically between five and fifteen milliseconds. The ISI distributions of Layer-II cells without DAPs peaked sharply at around four milliseconds and varied only minimally across that group. This dichotomy in burst behavior is explained by cell-group-specific DAP dynamics. The same two groups of bursting neurons also emerged when we clustered extracellular spike-train autocorrelations measured in real two-dimensional arenas (Latuske et al., 2015). No difference in the spatial coding properties of the grid cells across all three groups was discernible. Layer III neurons were only sparsely bursting and had no DAPs. As various mechanisms for modulating the ion-channels underlying DAPs exist, our results suggest that the temporal features of MEC activity can be altered while maintaining the cells’ spatial tuning characteristics.Significance StatementDepolarizing afterpotentials (DAPs) are frequently observed in principal neurons from slice preparations of rodent medial entorhinal cortex (MEC), but their functional role in vivo is unknown. Analyzing whole-cell data from mice running on virtual tracks, we show that DAPs do occur during behavior. Cells with prominent DAPs are found in Layer II; their inter-spike intervals reflect DAP time-scales. In contrast, neither the rarely bursting cells in Layer III, nor the high-frequency bursters in Layer II, have a DAP. Extracellular recordings from mice exploring real two-dimensional arenas demonstrate that grid cells within these three groups have rather similar spatial coding properties. We conclude that DAPs shape the temporal but not the spatial response characteristics of principal neurons in MEC.Author contributionsAll authors designed research. DÉC, CF, and JN performed research and analyzed data (equal contribution). AVMH wrote and edited the paper with support from MS and the other authors.

scholarly journals A Map-like Micro-Organization of Grid Cells in the Medial Entorhinal Cortex

Cell ◽  
2018 ◽  
Vol 175 (3) ◽  
pp. 736-750.e30 ◽  
Author(s):  
Yi Gu ◽  
Sam Lewallen ◽  
Amina A. Kinkhabwala ◽  
Cristina Domnisoru ◽  
Kijung Yoon ◽  
...  
Keyword(s):  
Entorhinal Cortex ◽  
Grid Cells ◽  
Medial Entorhinal Cortex

scholarly journals Home, head direction stability, and grid cell distortion

2020 ◽  
Vol 123 (4) ◽  
pp. 1392-1406 ◽  
Author(s):  
Juan Ignacio Sanguinetti-Scheck ◽  
Michael Brecht
Keyword(s):  
Entorhinal Cortex ◽  
Home Cage ◽  
Cell Activity ◽  
Grid Cell ◽  
Head Direction ◽  
Grid Cells ◽  
Head Direction Cells ◽  
Medial Entorhinal Cortex ◽  
Abstract Approach ◽  
Globally Stable

The home is a unique location in the life of humans and animals. In rats, home presents itself as a multicompartmental space that involves integrating navigation through subspaces. Here we embedded the laboratory rat’s home cage in the arena, while recording neurons in the animal’s parasubiculum and medial entorhinal cortex, two brain areas encoding the animal’s location and head direction. We found that head direction signals were unaffected by home cage presence or translocation. Head direction cells remain globally stable and have similar properties inside and outside the embedded home. We did not observe egocentric bearing encoding of the home cage. However, grid cells were distorted in the presence of the home cage. While they did not globally remap, single firing fields were translocated toward the home. These effects appeared to be geometrical in nature rather than a home-specific distortion and were not dependent on explicit behavioral use of the home cage during a hoarding task. Our work suggests that medial entorhinal cortex and parasubiculum do not remap after embedding the home, but local changes in grid cell activity overrepresent the embedded space location and might contribute to navigation in complex environments. NEW & NOTEWORTHY Neural findings in the field of spatial navigation come mostly from an abstract approach that separates the animal from even a minimally biological context. In this article we embed the home cage of the rat in the environment to address some of the complexities of natural navigation. We find no explicit home cage representation. While both head direction cells and grid cells remain globally stable, we find that embedded spaces locally distort grid cells.

scholarly journals Entorhinal cortex receptive fields are modulated by spatial attention, even without movement

eLife ◽  
2018 ◽  
Vol 7 ◽  
Author(s):  
Niklas Wilming ◽  
Peter König ◽  
Seth König ◽  
Elizabeth A Buffalo
Keyword(s):  
Entorhinal Cortex ◽  
Cell Activity ◽  
Receptive Fields ◽  
Grid Cell ◽  
Covert Attention ◽  
Grid Cells ◽  
Physical Movement ◽  
Mental Operations ◽  
Triangular Tiling ◽  
Central Fixation

Grid cells in the entorhinal cortex allow for the precise decoding of position in space. Along with potentially playing an important role in navigation, grid cells have recently been hypothesized to make a general contribution to mental operations. A prerequisite for this hypothesis is that grid cell activity does not critically depend on physical movement. Here, we show that movement of covert attention, without any physical movement, also elicits spatial receptive fields with a triangular tiling of space. In monkeys trained to maintain central fixation while covertly attending to a stimulus moving in the periphery we identified a significant population (20/141, 14% neurons at a FDR <5%) of entorhinal cells with spatially structured receptive fields. This contrasts with recordings obtained in the hippocampus, where grid-like representations were not observed. Our results provide evidence that neurons in macaque entorhinal cortex do not rely on physical movement.

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