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J Neurophysiol. 2015 Oct;114(4):2230-41. doi: 10.1152/jn.00188.2015. Epub 2015 Aug 5.

Rod- and cone-driven responses in mice expressing human L-cone pigment.

Author information

1
Department of Ophthalmology, University Hospital Erlangen, Erlangen, Germany; Department of Biology, Division of Animal Physiology, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany;
2
Vision Sciences, University of Washington, Seattle, Washington;
3
Department of Ophthalmology, University Hospital Erlangen, Erlangen, Germany; Department of Anatomy II, University of Erlangen-Nürnberg, Germany; and School of Optometry and Vision Science, University of Bradford, Bradford, United Kingdom jan.kremers@uk-erlangen.de.

Abstract

The mouse is commonly used for studying retinal processing, primarily because it is amenable to genetic manipulation. To accurately study photoreceptor driven signals in the healthy and diseased retina, it is of great importance to isolate the responses of single photoreceptor types. This is not easily achieved in mice because of the strong overlap of rod and M-cone absorption spectra (i.e., maxima at 498 and 508 nm, respectively). With a newly developed mouse model (Opn1lw(LIAIS)) expressing a variant of the human L-cone pigment (561 nm) instead of the mouse M-opsin, the absorption spectra are substantially separated, allowing retinal physiology to be studied using silent substitution stimuli. Unlike conventional chromatic isolation methods, this spectral compensation approach can isolate single photoreceptor subtypes without changing the retinal adaptation. We measured flicker electroretinograms in these mutants under ketamine-xylazine sedation with double silent substitution (silent S-cone and either rod or M/L-cones) and obtained robust responses for both rods and (L-)cones. Small signals were yielded in wild-type mice, whereas heterozygotes exhibited responses that were generally intermediate to both. Fundamental response amplitudes and phase behaviors (as a function of temporal frequency) in all genotypes were largely similar. Surprisingly, isolated (L-)cone and rod response properties in the mutant strain were alike. Thus the LIAIS mouse warrants a more comprehensive in vivo assessment of photoreceptor subtype-specific physiology, because it overcomes the hindrance of overlapping spectral sensitivities present in the normal mouse.

KEYWORDS:

keywords electrophysiology; mouse; photoreceptors; silent substitution

PMID:
26245314
PMCID:
PMC4600960
DOI:
10.1152/jn.00188.2015
[Indexed for MEDLINE]
Free PMC Article

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