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PMID: 11466416 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Constitutive "light" adaptation in rods from G90D rhodopsin: a mechanism for human congenital nightblindness without rod cell loss.

Sieving PA, Fowler ML, Bush RA, Machida S, Calvert PD, Green DG, Makino CL, McHenry CL

Abstract

A dominant form of human congenital nightblindness is caused by a gly90-->asp (G90D) mutation in rhodopsin. G90D has been shown to activate the phototransduction cascade in the absence of light in vitro. Such constitutive activity of G90D rhodopsin in vivo would desensitize rod photoreceptors and lead to nightblindness. In contrast, other rhodopsin mutations typically give rise to nightblindness by causing rod cell death. Thus, the proposed desensitization without rod degeneration would be a novel mechanism for this disorder. To explore this possibility, we induced mice to express G90D opsin in their rods and then examined rod function and morphology, after first crossing the transgenic animals with rhodopsin knock-out mice to obtain appropriate levels of opsin expression. The G90D mouse opsin bound the chromophore and formed a bleachable visual pigment with lambda(max) of 492 nm that supported rod photoresponses. (G+/-, R+/-) retinas, heterozygous for both G90D and wild-type (WT) rhodopsin, possessed normal numbers of photoreceptors and had a normal rhodopsin complement but exhibited considerable loss of rod sensitivity as measured electroretinographically. The rod photoresponses were desensitized, and the response time to peak was faster than in (R+/-) animals. An equivalent desensitization resulted by exposing WT retinas to a background light producing 82 photoisomerizations rod(-1) sec(-1), suggesting that G90D rods in darkness act as if they are partially "light-adapted." Adding a second G90D allele gave (G+/+, R+/-) animals that exhibited a further increase of equivalent background light level but had no rod cell loss by 24 weeks of age. (G+/+, R-/-) retinas that express only the mutant rhodopsin develop normal rod outer segments and show minimal rod cell loss even at 1 year of age. We conclude that G90D is constitutively active in mouse rods in vivo but that it does not cause significant rod degeneration. Instead, G90D desensitizes rods by a process equivalent to light adaptation.

MeSH Terms
Adaptation, Ocular/genetics Alleles Amino Acid Substitution Animals Cell Count Disease Models, Animal Dose-Response Relationship, Radiation Electroretinography Genes, Dominant Genotype Heterozygote Homozygote Humans Immunohistochemistry Light Mice Mice, Inbred BALB C Mice, Inbred C57BL Mice, Transgenic Night Blindness/etiology,physiopathology Retina/pathology,physiopathology Retinal Rod Photoreceptor Cells/pathology,physiopathology Rhodopsin/genetics,metabolism,radiation effects
Chemicals
Rhodopsin
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Sieving P A
Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, Michigan 48105, USA. psieving@umich.edu
Fowler M L
Bush R A
Machida S
Calvert P D
Green D G
Makino C L
McHenry C L
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Article Info
Journal
The Journal of neuroscience : the official journal of the Society for Neuroscience
Abbr.
J Neurosci
ISSN
1529-2401
Published
2001-08-01
Pages
5449-60
Language
English
Region
United States
NLM ID
8102140
PMCID
PMC6762654
Subset
IM
Grants
NEI NIH HHS · EY00379 · United States
NEI NIH HHS · EY06094 · United States
NEI NIH HHS · EY07003 · United States
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