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Characterisation of light responses in the retina of mice lacking principle components of rod, cone and melanopsin phototransduction signalling pathways

Gnat(−/−), Cnga3(−/−), Opn4(−/−) triple knockout (TKO) mice lack essential components of phototransduction signalling pathways present in rods, cones and photosensitive retinal ganglion cells (pRGCs), and are therefore expected to lack all sensitivity to light. However, a number of studies have show...

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Autores principales: Hughes, Steven, Rodgers, Jessica, Hickey, Doron, Foster, Russell G., Peirson, Stuart N., Hankins, Mark W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4908426/
https://www.ncbi.nlm.nih.gov/pubmed/27301998
http://dx.doi.org/10.1038/srep28086
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author Hughes, Steven
Rodgers, Jessica
Hickey, Doron
Foster, Russell G.
Peirson, Stuart N.
Hankins, Mark W.
author_facet Hughes, Steven
Rodgers, Jessica
Hickey, Doron
Foster, Russell G.
Peirson, Stuart N.
Hankins, Mark W.
author_sort Hughes, Steven
collection PubMed
description Gnat(−/−), Cnga3(−/−), Opn4(−/−) triple knockout (TKO) mice lack essential components of phototransduction signalling pathways present in rods, cones and photosensitive retinal ganglion cells (pRGCs), and are therefore expected to lack all sensitivity to light. However, a number of studies have shown that light responses persist in these mice. In this study we use multielectrode array (MEA) recordings and light-induced c-fos expression to further characterise the light responses of the TKO retina. Small, but robust electroretinogram type responses are routinely detected during MEA recordings, with properties consistent with rod driven responses. Furthermore, a distinctive pattern of light-induced c-fos expression is evident in the TKO retina, with c-fos expression largely restricted to a small subset of amacrine cells that express disabled-1 (Dab1) but lack expression of glycine transporter-1 (GlyT-1). Collectively these data are consistent with the persistence of a novel light sensing pathway in the TKO retina that originates in rod photoreceptors, potentially a rare subset of rods with distinct functional properties, and which is propagated to an atypical subtype of AII amacrine cells. Furthermore, the minimal responses observed following UV light stimulation suggest only a limited role for the non-visual opsin OPN5 in driving excitatory light responses within the mouse retina.
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spelling pubmed-49084262016-06-15 Characterisation of light responses in the retina of mice lacking principle components of rod, cone and melanopsin phototransduction signalling pathways Hughes, Steven Rodgers, Jessica Hickey, Doron Foster, Russell G. Peirson, Stuart N. Hankins, Mark W. Sci Rep Article Gnat(−/−), Cnga3(−/−), Opn4(−/−) triple knockout (TKO) mice lack essential components of phototransduction signalling pathways present in rods, cones and photosensitive retinal ganglion cells (pRGCs), and are therefore expected to lack all sensitivity to light. However, a number of studies have shown that light responses persist in these mice. In this study we use multielectrode array (MEA) recordings and light-induced c-fos expression to further characterise the light responses of the TKO retina. Small, but robust electroretinogram type responses are routinely detected during MEA recordings, with properties consistent with rod driven responses. Furthermore, a distinctive pattern of light-induced c-fos expression is evident in the TKO retina, with c-fos expression largely restricted to a small subset of amacrine cells that express disabled-1 (Dab1) but lack expression of glycine transporter-1 (GlyT-1). Collectively these data are consistent with the persistence of a novel light sensing pathway in the TKO retina that originates in rod photoreceptors, potentially a rare subset of rods with distinct functional properties, and which is propagated to an atypical subtype of AII amacrine cells. Furthermore, the minimal responses observed following UV light stimulation suggest only a limited role for the non-visual opsin OPN5 in driving excitatory light responses within the mouse retina. Nature Publishing Group 2016-06-15 /pmc/articles/PMC4908426/ /pubmed/27301998 http://dx.doi.org/10.1038/srep28086 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Hughes, Steven
Rodgers, Jessica
Hickey, Doron
Foster, Russell G.
Peirson, Stuart N.
Hankins, Mark W.
Characterisation of light responses in the retina of mice lacking principle components of rod, cone and melanopsin phototransduction signalling pathways
title Characterisation of light responses in the retina of mice lacking principle components of rod, cone and melanopsin phototransduction signalling pathways
title_full Characterisation of light responses in the retina of mice lacking principle components of rod, cone and melanopsin phototransduction signalling pathways
title_fullStr Characterisation of light responses in the retina of mice lacking principle components of rod, cone and melanopsin phototransduction signalling pathways
title_full_unstemmed Characterisation of light responses in the retina of mice lacking principle components of rod, cone and melanopsin phototransduction signalling pathways
title_short Characterisation of light responses in the retina of mice lacking principle components of rod, cone and melanopsin phototransduction signalling pathways
title_sort characterisation of light responses in the retina of mice lacking principle components of rod, cone and melanopsin phototransduction signalling pathways
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4908426/
https://www.ncbi.nlm.nih.gov/pubmed/27301998
http://dx.doi.org/10.1038/srep28086
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