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Photoreceptors in a mouse model of Leigh syndrome are capable of normal light-evoked signaling.

Publication ,  Journal Article
Gospe, SM; Travis, AM; Kolesnikov, AV; Klingeborn, M; Wang, L; Kefalov, VJ; Arshavsky, VY
Published in: J Biol Chem
August 16, 2019

Mitochondrial dysfunction is an important cause of heritable vision loss. Mutations affecting mitochondrial bioenergetics may lead to isolated vision loss or life-threatening systemic disease, depending on a mutation's severity. Primary optic nerve atrophy resulting from death of retinal ganglion cells is the most prominent ocular manifestation of mitochondrial disease. However, dysfunction of other retinal cell types has also been described, sometimes leading to a loss of photoreceptors and retinal pigment epithelium that manifests clinically as pigmentary retinopathy. A popular mouse model of mitochondrial disease that lacks NADH:ubiquinone oxidoreductase subunit S4 (NDUFS4), a subunit of mitochondrial complex I, phenocopies many traits of the human disease Leigh syndrome, including the development of optic atrophy. It has also been reported that ndufs4-/- mice display diminished light responses at the level of photoreceptors or bipolar cells. By conducting electroretinography (ERG) recordings in live ndufs4-/- mice, we now demonstrate that this defect occurs at the level of retinal photoreceptors. We found that this deficit does not arise from retinal developmental anomalies, photoreceptor degeneration, or impaired regeneration of visual pigment. Strikingly, the impairment of ndufs4-/- photoreceptor function was not observed in ex vivo ERG recordings from isolated retinas, indicating that photoreceptors with complex I deficiency are intrinsically capable of normal signaling. The difference in electrophysiological phenotypes in vivo and ex vivo suggests that the energy deprivation associated with severe mitochondrial impairment in the outer retina renders ndufs4-/- photoreceptors unable to maintain the homeostatic conditions required to operate at their normal capacity.

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Published In

J Biol Chem

DOI

EISSN

1083-351X

Publication Date

August 16, 2019

Volume

294

Issue

33

Start / End Page

12432 / 12443

Location

United States

Related Subject Headings

  • Retinal Degeneration
  • Photoreceptor Cells, Vertebrate
  • Mice, Knockout
  • Mice
  • Light Signal Transduction
  • Leigh Disease
  • Humans
  • Electroretinography
  • Electron Transport Complex I
  • Disease Models, Animal
 

Citation

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Gospe, S. M., Travis, A. M., Kolesnikov, A. V., Klingeborn, M., Wang, L., Kefalov, V. J., & Arshavsky, V. Y. (2019). Photoreceptors in a mouse model of Leigh syndrome are capable of normal light-evoked signaling. J Biol Chem, 294(33), 12432–12443. https://doi.org/10.1074/jbc.RA119.007945
Gospe, Sidney M., Amanda M. Travis, Alexander V. Kolesnikov, Mikael Klingeborn, Luyu Wang, Vladimir J. Kefalov, and Vadim Y. Arshavsky. “Photoreceptors in a mouse model of Leigh syndrome are capable of normal light-evoked signaling.J Biol Chem 294, no. 33 (August 16, 2019): 12432–43. https://doi.org/10.1074/jbc.RA119.007945.
Gospe SM, Travis AM, Kolesnikov AV, Klingeborn M, Wang L, Kefalov VJ, et al. Photoreceptors in a mouse model of Leigh syndrome are capable of normal light-evoked signaling. J Biol Chem. 2019 Aug 16;294(33):12432–43.
Gospe, Sidney M., et al. “Photoreceptors in a mouse model of Leigh syndrome are capable of normal light-evoked signaling.J Biol Chem, vol. 294, no. 33, Aug. 2019, pp. 12432–43. Pubmed, doi:10.1074/jbc.RA119.007945.
Gospe SM, Travis AM, Kolesnikov AV, Klingeborn M, Wang L, Kefalov VJ, Arshavsky VY. Photoreceptors in a mouse model of Leigh syndrome are capable of normal light-evoked signaling. J Biol Chem. 2019 Aug 16;294(33):12432–12443.

Published In

J Biol Chem

DOI

EISSN

1083-351X

Publication Date

August 16, 2019

Volume

294

Issue

33

Start / End Page

12432 / 12443

Location

United States

Related Subject Headings

  • Retinal Degeneration
  • Photoreceptor Cells, Vertebrate
  • Mice, Knockout
  • Mice
  • Light Signal Transduction
  • Leigh Disease
  • Humans
  • Electroretinography
  • Electron Transport Complex I
  • Disease Models, Animal