Literature DB >> 15994181

Opsin activation of transduction in the rods of dark-reared Rpe65 knockout mice.

Jie Fan1, Michael L Woodruff, Marianne C Cilluffo, Rosalie K Crouch, Gordon L Fain.   

Abstract

Rpe65 knockout mice (Rpe65-/-) are unable to synthesize the visual pigment chromophore 11-cis retinal; however, if these animals are reared in complete darkness, the rod photoreceptors accumulate a small amount of 9-cis retinal and its corresponding visual pigment isorhodopsin. Suction-electrode recording of single rods from dark-reared Rpe65-/- mice showed that the rods were about 400 times less sensitive than wild-type control rods and that the maximum responses were much smaller in amplitude. Spectral sensitivity measurements indicated that Rpe65-/- rod responses were generated by isorhodopsin rather than rhodopsin. Sensitivity and pigment concentration were compared in the same mice by measuring light responses from rods of one eye and pigment concentration from the retina of the other eye. Retinas had 11-35% of the normal pigment level, but the rods were of the order of 20-30 times less sensitive than could be accounted for by the loss in quantum catch. This extra desensitization must be caused by opsin-dependent activation of the visual cascade, which leads to a state equivalent to light adaptation in the dark-adapted rod. By comparing the sensitivity of dark-reared Rpe65-/- rods to that produced in normal rods by background light, we estimate that Rpe65-/- opsin is of the order of 2.5x10(-5) as efficient in activating transduction as photoactivated rhodopsin (Rh*) in WT mice. Dark-reared Rpe65-/- rods are less desensitized than rods from cyclic light-reared Rpe65-/- mice, have about 50% more photocurrent and degenerate at a slower rate. Retinas sectioned after 9 months in darkness show a larger number of photoreceptor nuclei in dark-reared animals than in cyclic light-reared animals, though both have fewer nuclei than in cyclic light-reared wild-type retinas. Both also have shorter outer segments and a lower free-Ca2+ concentration. These experiments provide the first quantitative measurement of opsin activation in physiologically responding mammalian rods.

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Year:  2005        PMID: 15994181      PMCID: PMC1474752          DOI: 10.1113/jphysiol.2005.091942

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  43 in total

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3.  Early-onset severe rod-cone dystrophy in young children with RPE65 mutations.

Authors:  B Lorenz; P Gyürüs; M Preising; D Bremser; S Gu; M Andrassi; C Gerth; A Gal
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Authors:  T YOSHIZAWA; G WALD
Journal:  Nature       Date:  1963-03-30       Impact factor: 49.962

5.  A comparison of the efficiency of G protein activation by ligand-free and light-activated forms of rhodopsin.

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6.  New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis.

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8.  Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis.

Authors:  H Morimura; G A Fishman; S A Grover; A B Fulton; E L Berson; T P Dryja
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9.  Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle.

Authors:  T M Redmond; S Yu; E Lee; D Bok; D Hamasaki; N Chen; P Goletz; J X Ma; R K Crouch; K Pfeifer
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2.  Bleaching of mouse rods: microspectrophotometry and suction-electrode recording.

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5.  Dark adaptation of human rod bipolar cells measured from the b-wave of the scotopic electroretinogram.

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Review 6.  Light and inherited retinal degeneration.

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7.  Dynamics of mouse rod phototransduction and its sensitivity to variation of key parameters.

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Review 8.  Constitutively active rhodopsin and retinal disease.

Authors:  Paul Shin-Hyun Park
Journal:  Adv Pharmacol       Date:  2014

9.  Apo-Opsin Exists in Equilibrium Between a Predominant Inactive and a Rare Highly Active State.

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