Dataset Information

Modularization of grid cells constrained by the pyramidal patch lattice.

ABSTRACT: Grid cells provide a metric representation of self-location. They are organized into modules, showing discretized scales of grid spacing, but the underlying mechanism remains elusive. In this modeling study, we propose that the hexagonal lattice of pyramidal cell patches may underlie the discretization of grid spacing and orientation. In the continuous attractor network composed of interneurons, stellate and pyramidal cells, the hexagonal lattice of bump attractors is specifically aligned to the patch lattice under 22 conditions determined by the geometry of the patch lattice, while pyramidal cells exhibit synchrony to diverse extents. Given the bump attractor lattice in each module originates from those 22 scenarios, the experimental data on the grid spacing ratio and orientation difference between modules can be reproduced. This work recapitulates the patterns of grid spacing versus orientation in individual animals and reveals the correlation between microstructures and firing fields, providing a systems-level mechanism for grid modularity.

SUBMITTER: Wang T

PROVIDER: S-EPMC8042349 | biostudies-literature | 2021 Apr

REPOSITORIES: biostudies-literature

ACCESS DATA

Publications

Modularization of grid cells constrained by the pyramidal patch lattice.

Wang Tao T Yang Fan F Wang Ziqun Z Zhang Bing B Wang Wei W Liu Feng F

iScience 20210317 4

Grid cells provide a metric representation of self-location. They are organized into modules, showing discretized scales of grid spacing, but the underlying mechanism remains elusive. In this modeling study, we propose that the hexagonal lattice of pyramidal cell patches may underlie the discretization of grid spacing and orientation. In the continuous attractor network composed of interneurons, stellate and pyramidal cells, the hexagonal lattice of bump attractors is specifically aligned to the ...[more]

PMID: 33870125

Similar Datasets

Project description:Mounting evidence shows mammalian brains are probabilistic computers, but the specific cells involved remain elusive. Parallel research suggests that grid cells of the mammalian hippocampal formation are fundamental to spatial cognition but their diverse response properties still defy explanation. No plausible model exists which explains stable grids in darkness for twenty minutes or longer, despite being one of the first results ever published on grid cells. Similarly, no current explanation can tie together grid fragmentation and grid rescaling, which show very different forms of flexibility in grid responses when the environment is varied. Other properties such as attractor dynamics and grid anisotropy seem to be at odds with one another unless additional properties are assumed such as a varying velocity gain. Modelling efforts have largely ignored the breadth of response patterns, while also failing to account for the disastrous effects of sensory noise during spatial learning and recall, especially in darkness. Here, published electrophysiological evidence from a range of experiments are reinterpreted using a novel probabilistic learning model, which shows that grid cell responses are accurately predicted by a probabilistic learning process. Diverse response properties of probabilistic grid cells are statistically indistinguishable from rat grid cells across key manipulations. A simple coherent set of probabilistic computations explains stable grid fields in darkness, partial grid rescaling in resized arenas, low-dimensional attractor grid cell dynamics, and grid fragmentation in hairpin mazes. The same computations also reconcile oscillatory dynamics at the single cell level with attractor dynamics at the cell ensemble level. Additionally, a clear functional role for boundary cells is proposed for spatial learning. These findings provide a parsimonious and unified explanation of grid cell function, and implicate grid cells as an accessible neuronal population readout of a set of probabilistic spatial computations.

Project description:The lack of established standards to describe and annotate biological assays and screening outcomes in the domain of drug and chemical probe discovery is a severe limitation to utilize public and proprietary drug screening data to their maximum potential. We have created the BioAssay Ontology (BAO) project (http://bioassayontology.org) to develop common reference metadata terms and definitions required for describing relevant information of low-and high-throughput drug and probe screening assays and results. The main objectives of BAO are to enable effective integration, aggregation, retrieval, and analyses of drug screening data. Since we first released BAO on the BioPortal in 2010 we have considerably expanded and enhanced BAO and we have applied the ontology in several internal and external collaborative projects, for example the BioAssay Research Database (BARD). We describe the evolution of BAO with a design that enables modeling complex assays including profile and panel assays such as those in the Library of Integrated Network-based Cellular Signatures (LINCS). One of the critical questions in evolving BAO is the following: how can we provide a way to efficiently reuse and share among various research projects specific parts of our ontologies without violating the integrity of the ontology and without creating redundancies. This paper provides a comprehensive answer to this question with a description of a methodology for ontology modularization using a layered architecture. Our modularization approach defines several distinct BAO components and separates internal from external modules and domain-level from structural components. This approach facilitates the generation/extraction of derived ontologies (or perspectives) that can suit particular use cases or software applications. We describe the evolution of BAO related to its formal structures, engineering approaches, and content to enable modeling of complex assays and integration with other ontologies and datasets.

Dataset Information

Modularization of grid cells constrained by the pyramidal patch lattice.

Publications

Modularization of grid cells constrained by the pyramidal patch lattice.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets