Cellular adaptation facilitates sparse and reliable coding in sensory pathways.

Most neurons in peripheral sensory pathways initially respond vigorously when a preferred stimulus is presented, but adapt as stimulation continues. It is unclear how this phenomenon affects stimulus coding in the later stages of sensory processing. Here, we show that a temporally sparse and reliabl...

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Main Authors: Farzad Farkhooi, Anja Froese, Eilif Muller, Randolf Menzel, Martin P Nawrot
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC3789775?pdf=render
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spelling doaj-e5fa1fa4001942efa741d65244d600352020-11-25T02:31:46ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582013-01-01910e100325110.1371/journal.pcbi.1003251Cellular adaptation facilitates sparse and reliable coding in sensory pathways.Farzad FarkhooiAnja FroeseEilif MullerRandolf MenzelMartin P NawrotMost neurons in peripheral sensory pathways initially respond vigorously when a preferred stimulus is presented, but adapt as stimulation continues. It is unclear how this phenomenon affects stimulus coding in the later stages of sensory processing. Here, we show that a temporally sparse and reliable stimulus representation develops naturally in sequential stages of a sensory network with adapting neurons. As a modeling framework we employ a mean-field approach together with an adaptive population density treatment, accompanied by numerical simulations of spiking neural networks. We find that cellular adaptation plays a critical role in the dynamic reduction of the trial-by-trial variability of cortical spike responses by transiently suppressing self-generated fast fluctuations in the cortical balanced network. This provides an explanation for a widespread cortical phenomenon by a simple mechanism. We further show that in the insect olfactory system cellular adaptation is sufficient to explain the emergence of the temporally sparse and reliable stimulus representation in the mushroom body. Our results reveal a generic, biophysically plausible mechanism that can explain the emergence of a temporally sparse and reliable stimulus representation within a sequential processing architecture.http://europepmc.org/articles/PMC3789775?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Farzad Farkhooi
Anja Froese
Eilif Muller
Randolf Menzel
Martin P Nawrot
spellingShingle Farzad Farkhooi
Anja Froese
Eilif Muller
Randolf Menzel
Martin P Nawrot
Cellular adaptation facilitates sparse and reliable coding in sensory pathways.
PLoS Computational Biology
author_facet Farzad Farkhooi
Anja Froese
Eilif Muller
Randolf Menzel
Martin P Nawrot
author_sort Farzad Farkhooi
title Cellular adaptation facilitates sparse and reliable coding in sensory pathways.
title_short Cellular adaptation facilitates sparse and reliable coding in sensory pathways.
title_full Cellular adaptation facilitates sparse and reliable coding in sensory pathways.
title_fullStr Cellular adaptation facilitates sparse and reliable coding in sensory pathways.
title_full_unstemmed Cellular adaptation facilitates sparse and reliable coding in sensory pathways.
title_sort cellular adaptation facilitates sparse and reliable coding in sensory pathways.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2013-01-01
description Most neurons in peripheral sensory pathways initially respond vigorously when a preferred stimulus is presented, but adapt as stimulation continues. It is unclear how this phenomenon affects stimulus coding in the later stages of sensory processing. Here, we show that a temporally sparse and reliable stimulus representation develops naturally in sequential stages of a sensory network with adapting neurons. As a modeling framework we employ a mean-field approach together with an adaptive population density treatment, accompanied by numerical simulations of spiking neural networks. We find that cellular adaptation plays a critical role in the dynamic reduction of the trial-by-trial variability of cortical spike responses by transiently suppressing self-generated fast fluctuations in the cortical balanced network. This provides an explanation for a widespread cortical phenomenon by a simple mechanism. We further show that in the insect olfactory system cellular adaptation is sufficient to explain the emergence of the temporally sparse and reliable stimulus representation in the mushroom body. Our results reveal a generic, biophysically plausible mechanism that can explain the emergence of a temporally sparse and reliable stimulus representation within a sequential processing architecture.
url http://europepmc.org/articles/PMC3789775?pdf=render
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