| Title: |
Opa1 and MT-Nd6 mutations induce early mitochondrial changes in the retina and prelaminar optic nerve of hereditary optic neuropathy mouse models |
| Authors: |
Bureau, Jacques; Manero, Florence; Baris, Olivier; Bodin, Alexia; Verny, Christophe; Chevrollier, Arnaud; Lenaers, Guy; Codron, Philippe |
| Contributors: |
French National Scientific Research Council; French National Institute for Health and Medical Research; University of Angers; Retina France; Ouvrir-Les-Yeux and Kjer-France |
| Source: |
Brain Communications ; volume 6, issue 6 ; ISSN 2632-1297 |
| Publisher Information: |
Oxford University Press (OUP) |
| Publication Year: |
2024 |
| Description: |
Hereditary optic neuropathies, including dominant optic atrophy and Leber’s hereditary optic neuropathy, are genetic disorders characterized by retinal ganglion cell degeneration leading to vision loss, mainly associated with mitochondrial dysfunction. In this study, we analysed mitochondrial distribution and ultrastructure in the retina and longitudinal optic nerve sections of pre-symptomatic hereditary optic neuropathies mouse models with Opa1 and Nd6 deficiency to identify early mitochondrial changes. Our results show significant mitochondrial fragmentation and increased mitophagy in Opa1+/− mice, indicating early mitochondrial changes prior to neuronal loss. Conversely, Nd6P25L mice exhibited mitochondrial hypertrophy, suggesting an adaptive response to compensate for altered energy metabolism. These pre-symptomatic mitochondrial changes were mainly observed in the unmyelinated portion of the retinal ganglion cell axons, where the transmission of the visual information requires high energy expenditure, constituting the specific point of vulnerability in hereditary optic neuropathies. These findings highlight early focal mitochondrial changes prior to neuronal loss in hereditary optic neuropathies and provide insight into pre-symptomatic therapeutic approaches. |
| Document Type: |
article in journal/newspaper |
| Language: |
English |
| DOI: |
10.1093/braincomms/fcae404 |
| DOI: |
10.1093/braincomms/fcae404/60643269/fcae404.pdf |
| Availability: |
https://doi.org/10.1093/braincomms/fcae404; https://academic.oup.com/braincomms/advance-article-pdf/doi/10.1093/braincomms/fcae404/60643269/fcae404.pdf; https://academic.oup.com/braincomms/article-pdf/6/6/fcae404/60966645/fcae404.pdf |
| Rights: |
https://creativecommons.org/licenses/by/4.0/ |
| Accession Number: |
edsbas.FDFCF36A |
| Database: |
BASE |