Cargando…

Coordinated dynamic encoding in the retina using opposing forms of plasticity

The range of natural inputs encoded by a neuron often exceeds its dynamic range. To overcome this limitation, neural populations divide their inputs among different cell classes, as with rod and cone photoreceptors, and adapt by shifting their dynamic range. We report that the dynamic behavior of re...

Descripción completa

Detalles Bibliográficos
Autores principales: Kastner, David B., Baccus, Stephen A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359137/
https://www.ncbi.nlm.nih.gov/pubmed/21909086
http://dx.doi.org/10.1038/nn.2906
_version_ 1782233821928751104
author Kastner, David B.
Baccus, Stephen A.
author_facet Kastner, David B.
Baccus, Stephen A.
author_sort Kastner, David B.
collection PubMed
description The range of natural inputs encoded by a neuron often exceeds its dynamic range. To overcome this limitation, neural populations divide their inputs among different cell classes, as with rod and cone photoreceptors, and adapt by shifting their dynamic range. We report that the dynamic behavior of retinal ganglion cells in salamanders, mice, and rabbits is divided into two opposing forms of short-term plasticity in different cell classes. One population of cells exhibited sensitization—a persistent elevated sensitivity following a strong stimulus. This novel dynamic behavior compensates for the information loss caused by the known process of adaptation occurring in a separate cell population. The two populations divide the dynamic range of inputs, with sensitizing cells encoding weak signals, and adapting cells encoding strong signals. In the two populations, the linear, threshold and adaptive properties are linked to preserve responsiveness when stimulus statistics change, with one population maintaining the ability to respond when the other fails.
format Online
Article
Text
id pubmed-3359137
institution National Center for Biotechnology Information
language English
publishDate 2011
record_format MEDLINE/PubMed
spelling pubmed-33591372012-05-23 Coordinated dynamic encoding in the retina using opposing forms of plasticity Kastner, David B. Baccus, Stephen A. Nat Neurosci Article The range of natural inputs encoded by a neuron often exceeds its dynamic range. To overcome this limitation, neural populations divide their inputs among different cell classes, as with rod and cone photoreceptors, and adapt by shifting their dynamic range. We report that the dynamic behavior of retinal ganglion cells in salamanders, mice, and rabbits is divided into two opposing forms of short-term plasticity in different cell classes. One population of cells exhibited sensitization—a persistent elevated sensitivity following a strong stimulus. This novel dynamic behavior compensates for the information loss caused by the known process of adaptation occurring in a separate cell population. The two populations divide the dynamic range of inputs, with sensitizing cells encoding weak signals, and adapting cells encoding strong signals. In the two populations, the linear, threshold and adaptive properties are linked to preserve responsiveness when stimulus statistics change, with one population maintaining the ability to respond when the other fails. 2011-09-11 /pmc/articles/PMC3359137/ /pubmed/21909086 http://dx.doi.org/10.1038/nn.2906 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Kastner, David B.
Baccus, Stephen A.
Coordinated dynamic encoding in the retina using opposing forms of plasticity
title Coordinated dynamic encoding in the retina using opposing forms of plasticity
title_full Coordinated dynamic encoding in the retina using opposing forms of plasticity
title_fullStr Coordinated dynamic encoding in the retina using opposing forms of plasticity
title_full_unstemmed Coordinated dynamic encoding in the retina using opposing forms of plasticity
title_short Coordinated dynamic encoding in the retina using opposing forms of plasticity
title_sort coordinated dynamic encoding in the retina using opposing forms of plasticity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359137/
https://www.ncbi.nlm.nih.gov/pubmed/21909086
http://dx.doi.org/10.1038/nn.2906
work_keys_str_mv AT kastnerdavidb coordinateddynamicencodingintheretinausingopposingformsofplasticity
AT baccusstephena coordinateddynamicencodingintheretinausingopposingformsofplasticity