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Ambra1 haploinsufficiency in CD1 mice results in metabolic alterations and exacerbates age-associated retinal degeneration

Macroautophagy/autophagy is a key process in the maintenance of cellular homeostasis. The age-dependent decline in retinal autophagy has been associated with photoreceptor degeneration. Retinal dysfunction can also result from damage to the retinal pigment epithelium (RPE), as the RPE-retina constit...

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Autores principales: Ramírez-Pardo, Ignacio, Villarejo-Zori, Beatriz, Jiménez-Loygorri, Juan Ignacio, Sierra-Filardi, Elena, Alonso-Gil, Sandra, Mariño, Guillermo, de la Villa, Pedro, Fitze, Patrick S, Fuentes, José Manuel, García-Escudero, Ramón, Ferrington, Deborah A., Gomez-Sintes, Raquel, Boya, Patricia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980615/
https://www.ncbi.nlm.nih.gov/pubmed/35875981
http://dx.doi.org/10.1080/15548627.2022.2103307
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author Ramírez-Pardo, Ignacio
Villarejo-Zori, Beatriz
Jiménez-Loygorri, Juan Ignacio
Sierra-Filardi, Elena
Alonso-Gil, Sandra
Mariño, Guillermo
de la Villa, Pedro
Fitze, Patrick S
Fuentes, José Manuel
García-Escudero, Ramón
Ferrington, Deborah A.
Gomez-Sintes, Raquel
Boya, Patricia
author_facet Ramírez-Pardo, Ignacio
Villarejo-Zori, Beatriz
Jiménez-Loygorri, Juan Ignacio
Sierra-Filardi, Elena
Alonso-Gil, Sandra
Mariño, Guillermo
de la Villa, Pedro
Fitze, Patrick S
Fuentes, José Manuel
García-Escudero, Ramón
Ferrington, Deborah A.
Gomez-Sintes, Raquel
Boya, Patricia
author_sort Ramírez-Pardo, Ignacio
collection PubMed
description Macroautophagy/autophagy is a key process in the maintenance of cellular homeostasis. The age-dependent decline in retinal autophagy has been associated with photoreceptor degeneration. Retinal dysfunction can also result from damage to the retinal pigment epithelium (RPE), as the RPE-retina constitutes an important metabolic ecosystem that must be finely tuned to preserve visual function. While studies of mice lacking essential autophagy genes have revealed a predisposition to retinal degeneration, the consequences of a moderate reduction in autophagy, similar to that which occurs during physiological aging, remain unclear. Here, we described a retinal phenotype consistent with accelerated aging in mice carrying a haploinsufficiency for Ambra1, a pro-autophagic gene. These mice showed protein aggregation in the retina and RPE, metabolic underperformance, and premature vision loss. Moreover, Ambra1(+/gt) mice were more prone to retinal degeneration after RPE stress. These findings indicate that autophagy provides crucial support to RPE-retinal metabolism and protects the retina against stress and physiological aging. Abbreviations : 4-HNE: 4-hydroxynonenal; AMBRA1: autophagy and beclin 1 regulator 1, AMD: age-related macular degeneration;; GCL: ganglion cell layer; GFAP: glial fibrillary acidic protein; GLUL: glutamine synthetase/glutamate-ammonia ligase; HCL: hierarchical clustering; INL: inner nuclear layer; IPL: inner plexiform layer; LC/GC-MS: liquid chromatography/gas chromatography–mass spectrometry; MA: middle-aged; MTDR: MitoTracker Deep Red; MFI: mean fluorescence intensity; NL: NH(4)Cl and leupeptin; Nqo: NAD(P)H quinone dehydrogenase; ONL: outer nuclear layer; OPL: outer plexiform layer; OP: oscillatory potentials; OXPHOS: oxidative phosphorylation; PCR: polymerase chain reaction; PRKC/PKCα: protein kinase C; POS: photoreceptor outer segment; RGC: retinal ganglion cells; RPE: retinal pigment epithelium; SI: sodium iodate; TCA: tricarboxylic acid.
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spelling pubmed-99806152023-03-03 Ambra1 haploinsufficiency in CD1 mice results in metabolic alterations and exacerbates age-associated retinal degeneration Ramírez-Pardo, Ignacio Villarejo-Zori, Beatriz Jiménez-Loygorri, Juan Ignacio Sierra-Filardi, Elena Alonso-Gil, Sandra Mariño, Guillermo de la Villa, Pedro Fitze, Patrick S Fuentes, José Manuel García-Escudero, Ramón Ferrington, Deborah A. Gomez-Sintes, Raquel Boya, Patricia Autophagy Research Paper Macroautophagy/autophagy is a key process in the maintenance of cellular homeostasis. The age-dependent decline in retinal autophagy has been associated with photoreceptor degeneration. Retinal dysfunction can also result from damage to the retinal pigment epithelium (RPE), as the RPE-retina constitutes an important metabolic ecosystem that must be finely tuned to preserve visual function. While studies of mice lacking essential autophagy genes have revealed a predisposition to retinal degeneration, the consequences of a moderate reduction in autophagy, similar to that which occurs during physiological aging, remain unclear. Here, we described a retinal phenotype consistent with accelerated aging in mice carrying a haploinsufficiency for Ambra1, a pro-autophagic gene. These mice showed protein aggregation in the retina and RPE, metabolic underperformance, and premature vision loss. Moreover, Ambra1(+/gt) mice were more prone to retinal degeneration after RPE stress. These findings indicate that autophagy provides crucial support to RPE-retinal metabolism and protects the retina against stress and physiological aging. Abbreviations : 4-HNE: 4-hydroxynonenal; AMBRA1: autophagy and beclin 1 regulator 1, AMD: age-related macular degeneration;; GCL: ganglion cell layer; GFAP: glial fibrillary acidic protein; GLUL: glutamine synthetase/glutamate-ammonia ligase; HCL: hierarchical clustering; INL: inner nuclear layer; IPL: inner plexiform layer; LC/GC-MS: liquid chromatography/gas chromatography–mass spectrometry; MA: middle-aged; MTDR: MitoTracker Deep Red; MFI: mean fluorescence intensity; NL: NH(4)Cl and leupeptin; Nqo: NAD(P)H quinone dehydrogenase; ONL: outer nuclear layer; OPL: outer plexiform layer; OP: oscillatory potentials; OXPHOS: oxidative phosphorylation; PCR: polymerase chain reaction; PRKC/PKCα: protein kinase C; POS: photoreceptor outer segment; RGC: retinal ganglion cells; RPE: retinal pigment epithelium; SI: sodium iodate; TCA: tricarboxylic acid. Taylor & Francis 2022-07-24 /pmc/articles/PMC9980615/ /pubmed/35875981 http://dx.doi.org/10.1080/15548627.2022.2103307 Text en © 2022 CSIC. Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Ramírez-Pardo, Ignacio
Villarejo-Zori, Beatriz
Jiménez-Loygorri, Juan Ignacio
Sierra-Filardi, Elena
Alonso-Gil, Sandra
Mariño, Guillermo
de la Villa, Pedro
Fitze, Patrick S
Fuentes, José Manuel
García-Escudero, Ramón
Ferrington, Deborah A.
Gomez-Sintes, Raquel
Boya, Patricia
Ambra1 haploinsufficiency in CD1 mice results in metabolic alterations and exacerbates age-associated retinal degeneration
title Ambra1 haploinsufficiency in CD1 mice results in metabolic alterations and exacerbates age-associated retinal degeneration
title_full Ambra1 haploinsufficiency in CD1 mice results in metabolic alterations and exacerbates age-associated retinal degeneration
title_fullStr Ambra1 haploinsufficiency in CD1 mice results in metabolic alterations and exacerbates age-associated retinal degeneration
title_full_unstemmed Ambra1 haploinsufficiency in CD1 mice results in metabolic alterations and exacerbates age-associated retinal degeneration
title_short Ambra1 haploinsufficiency in CD1 mice results in metabolic alterations and exacerbates age-associated retinal degeneration
title_sort ambra1 haploinsufficiency in cd1 mice results in metabolic alterations and exacerbates age-associated retinal degeneration
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980615/
https://www.ncbi.nlm.nih.gov/pubmed/35875981
http://dx.doi.org/10.1080/15548627.2022.2103307
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