Successful amelioration of mitochondrial optic neuropathy using the yeast NDI1 gene in a rat animal model.

Leber's hereditary optic neuropathy (LHON) is a maternally inherited disorder with point mutations in mitochondrial DNA which result in loss of vision in young adults. The majority of mutations reported to date are within the genes encoding the subunits of the mitochondrial NADH-quinone oxidore...

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Main Authors: Mathieu Marella, Byoung Boo Seo, Biju B Thomas, Akemi Matsuno-Yagi, Takao Yagi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-07-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2900204?pdf=render
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spelling doaj-29af6a0d53544d5780b200b998bd9bbd2020-11-25T01:55:54ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-07-0157e1147210.1371/journal.pone.0011472Successful amelioration of mitochondrial optic neuropathy using the yeast NDI1 gene in a rat animal model.Mathieu MarellaByoung Boo SeoBiju B ThomasAkemi Matsuno-YagiTakao YagiLeber's hereditary optic neuropathy (LHON) is a maternally inherited disorder with point mutations in mitochondrial DNA which result in loss of vision in young adults. The majority of mutations reported to date are within the genes encoding the subunits of the mitochondrial NADH-quinone oxidoreductase, complex I. Establishment of animal models of LHON should help elucidate mechanism of the disease and could be utilized for possible development of therapeutic strategies.We established a rat model which involves injection of rotenone-loaded microspheres into the optic layer of the rat superior colliculus. The animals exhibited the most common features of LHON. Visual loss was observed within 2 weeks of rotenone administration with no apparent effect on retinal ganglion cells. Death of retinal ganglion cells occurred at a later stage. Using our rat model, we investigated the effect of the yeast alternative NADH dehydrogenase, Ndi1. We were able to achieve efficient expression of the Ndi1 protein in the mitochondria of all regions of retinal ganglion cells and axons by delivering the NDI1 gene into the optical layer of the superior colliculus. Remarkably, even after the vision of the rats was severely impaired, treatment of the animals with the NDI1 gene led to a complete restoration of the vision to the normal level. Control groups that received either empty vector or the GFP gene had no effects.The present study reports successful manifestation of LHON-like symptoms in rats and demonstrates the potential of the NDI1 gene therapy on mitochondrial optic neuropathies. Our results indicate a window of opportunity for the gene therapy to be applied successfully after the onset of the disease symptoms.http://europepmc.org/articles/PMC2900204?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Mathieu Marella
Byoung Boo Seo
Biju B Thomas
Akemi Matsuno-Yagi
Takao Yagi
spellingShingle Mathieu Marella
Byoung Boo Seo
Biju B Thomas
Akemi Matsuno-Yagi
Takao Yagi
Successful amelioration of mitochondrial optic neuropathy using the yeast NDI1 gene in a rat animal model.
PLoS ONE
author_facet Mathieu Marella
Byoung Boo Seo
Biju B Thomas
Akemi Matsuno-Yagi
Takao Yagi
author_sort Mathieu Marella
title Successful amelioration of mitochondrial optic neuropathy using the yeast NDI1 gene in a rat animal model.
title_short Successful amelioration of mitochondrial optic neuropathy using the yeast NDI1 gene in a rat animal model.
title_full Successful amelioration of mitochondrial optic neuropathy using the yeast NDI1 gene in a rat animal model.
title_fullStr Successful amelioration of mitochondrial optic neuropathy using the yeast NDI1 gene in a rat animal model.
title_full_unstemmed Successful amelioration of mitochondrial optic neuropathy using the yeast NDI1 gene in a rat animal model.
title_sort successful amelioration of mitochondrial optic neuropathy using the yeast ndi1 gene in a rat animal model.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2010-07-01
description Leber's hereditary optic neuropathy (LHON) is a maternally inherited disorder with point mutations in mitochondrial DNA which result in loss of vision in young adults. The majority of mutations reported to date are within the genes encoding the subunits of the mitochondrial NADH-quinone oxidoreductase, complex I. Establishment of animal models of LHON should help elucidate mechanism of the disease and could be utilized for possible development of therapeutic strategies.We established a rat model which involves injection of rotenone-loaded microspheres into the optic layer of the rat superior colliculus. The animals exhibited the most common features of LHON. Visual loss was observed within 2 weeks of rotenone administration with no apparent effect on retinal ganglion cells. Death of retinal ganglion cells occurred at a later stage. Using our rat model, we investigated the effect of the yeast alternative NADH dehydrogenase, Ndi1. We were able to achieve efficient expression of the Ndi1 protein in the mitochondria of all regions of retinal ganglion cells and axons by delivering the NDI1 gene into the optical layer of the superior colliculus. Remarkably, even after the vision of the rats was severely impaired, treatment of the animals with the NDI1 gene led to a complete restoration of the vision to the normal level. Control groups that received either empty vector or the GFP gene had no effects.The present study reports successful manifestation of LHON-like symptoms in rats and demonstrates the potential of the NDI1 gene therapy on mitochondrial optic neuropathies. Our results indicate a window of opportunity for the gene therapy to be applied successfully after the onset of the disease symptoms.
url http://europepmc.org/articles/PMC2900204?pdf=render
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