Does the Entorhinal Cortex use the Fourier Transform?

Some neurons in the entorhinal cortex (EC) fire bursts when the animal occupies locations organized in a hexagonal grid pattern in their spatial environment. Place cells have also been observed, firing bursts only when the animal occupies a particular region of the environment. Both of these types o...

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Main Authors: Jeff eOrchard, Hao eYang, Xiang eJi
Format: Article
Language:English
Published: Frontiers Media S.A. 2013-12-01
Series:Frontiers in Computational Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fncom.2013.00179/full
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spelling doaj-228d4218bf2e444aaed669af155adc922020-11-24T21:56:11ZengFrontiers Media S.A.Frontiers in Computational Neuroscience1662-51882013-12-01710.3389/fncom.2013.0017940167Does the Entorhinal Cortex use the Fourier Transform?Jeff eOrchard0Hao eYang1Xiang eJi2University of WaterlooUniversity of WaterlooUniversity of WaterlooSome neurons in the entorhinal cortex (EC) fire bursts when the animal occupies locations organized in a hexagonal grid pattern in their spatial environment. Place cells have also been observed, firing bursts only when the animal occupies a particular region of the environment. Both of these types of cells exhibit theta-cycle modulation, firing bursts in the 4-12Hz range. Grid cells fire bursts of action potentials that precess with respect to the theta cycle, a phenomenon dubbed "theta precession". Various models have been proposed to explain these phenomena, and how they relate to navigation. Among the most promising are the oscillator interference models. The bank-of-oscillators model proposed by Welday et al. (2011) exhibits all these features. However, their simulations are based on theoretical oscillators, and not implemented entirely with spiking neurons. We extend their work in a number of ways. First, we place the oscillators in a frequency domain and reformulate the model in terms of Fourier theory. Second, this perspective suggests a division of labour for implementing spatial maps: position, versus map layout. The animal's position is encoded in the phases of the oscillators, while the spatial map shape is encoded implicitly in the weights of the connections between the oscillators and the read-out nodes. Third, it reveals that the oscillator phases all need to conform to a linear relationship across the frequency domain. Fourth, we implement a partial model of the EC using spiking leaky integrate-and-fire (LIF) neurons. Fifth, we devise new coupling mechanisms, enlightened by the global phase constraint, and show they are capable of keeping spiking neural oscillators in consistent formation. Our model demonstrates place cells, grid cells, and phase precession. The Fourier model also gives direction for future investigations, such as integrating sensory feedback to combat drift, or explaining why grid cells exist at all.http://journal.frontiersin.org/Journal/10.3389/fncom.2013.00179/fullEntorhinal Cortexpath integrationgrid cellsPlace CellsFourier Transformneural engineering framework
collection DOAJ
language English
format Article
sources DOAJ
author Jeff eOrchard
Hao eYang
Xiang eJi
spellingShingle Jeff eOrchard
Hao eYang
Xiang eJi
Does the Entorhinal Cortex use the Fourier Transform?
Frontiers in Computational Neuroscience
Entorhinal Cortex
path integration
grid cells
Place Cells
Fourier Transform
neural engineering framework
author_facet Jeff eOrchard
Hao eYang
Xiang eJi
author_sort Jeff eOrchard
title Does the Entorhinal Cortex use the Fourier Transform?
title_short Does the Entorhinal Cortex use the Fourier Transform?
title_full Does the Entorhinal Cortex use the Fourier Transform?
title_fullStr Does the Entorhinal Cortex use the Fourier Transform?
title_full_unstemmed Does the Entorhinal Cortex use the Fourier Transform?
title_sort does the entorhinal cortex use the fourier transform?
publisher Frontiers Media S.A.
series Frontiers in Computational Neuroscience
issn 1662-5188
publishDate 2013-12-01
description Some neurons in the entorhinal cortex (EC) fire bursts when the animal occupies locations organized in a hexagonal grid pattern in their spatial environment. Place cells have also been observed, firing bursts only when the animal occupies a particular region of the environment. Both of these types of cells exhibit theta-cycle modulation, firing bursts in the 4-12Hz range. Grid cells fire bursts of action potentials that precess with respect to the theta cycle, a phenomenon dubbed "theta precession". Various models have been proposed to explain these phenomena, and how they relate to navigation. Among the most promising are the oscillator interference models. The bank-of-oscillators model proposed by Welday et al. (2011) exhibits all these features. However, their simulations are based on theoretical oscillators, and not implemented entirely with spiking neurons. We extend their work in a number of ways. First, we place the oscillators in a frequency domain and reformulate the model in terms of Fourier theory. Second, this perspective suggests a division of labour for implementing spatial maps: position, versus map layout. The animal's position is encoded in the phases of the oscillators, while the spatial map shape is encoded implicitly in the weights of the connections between the oscillators and the read-out nodes. Third, it reveals that the oscillator phases all need to conform to a linear relationship across the frequency domain. Fourth, we implement a partial model of the EC using spiking leaky integrate-and-fire (LIF) neurons. Fifth, we devise new coupling mechanisms, enlightened by the global phase constraint, and show they are capable of keeping spiking neural oscillators in consistent formation. Our model demonstrates place cells, grid cells, and phase precession. The Fourier model also gives direction for future investigations, such as integrating sensory feedback to combat drift, or explaining why grid cells exist at all.
topic Entorhinal Cortex
path integration
grid cells
Place Cells
Fourier Transform
neural engineering framework
url http://journal.frontiersin.org/Journal/10.3389/fncom.2013.00179/full
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