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

Abstract:
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.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/srep28086

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Clinical Neurosciences
Role:
Author


More from this funder
Grant:
090684/Z/09/Z
090684/Z/09/Z
Funding agency for:
Foster, R
More from this funder
Grant:
BB/M009998/1
BB/M009998/1
Funding agency for:
Hankins, M


Publisher:
Nature Publishing Group
Journal:
Scientific Reports More from this journal
Volume:
7
Article number:
28086
Publication date:
2016-06-01
Acceptance date:
2016-05-26
DOI:
ISSN:
2045-2322


Pubs id:
pubs:627016
UUID:
uuid:04dd46db-58f4-44be-ad78-75a4596fb18e
Local pid:
pubs:627016
Source identifiers:
627016
Deposit date:
2016-06-09
ARK identifier:

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