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Characterization of the role of autophagy in retinal ganglion cell survival over time using a rat model of chronic ocular hypertension

Autophagy is an essential cellular process for the degradation and recycling of cellular components, and its dysregulation has been linked to neuronal cell death and neurodegeneration. In glaucoma, the role of autophagy in retinal ganglion cell (RGC) survival remains contradictory. Moreover, the eff...

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Autores principales: Lee, Si Hyung, Shim, Kyung Sun, Kim, Chan Yun, Park, Tae Kwann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952572/
https://www.ncbi.nlm.nih.gov/pubmed/33707562
http://dx.doi.org/10.1038/s41598-021-85181-x
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author Lee, Si Hyung
Shim, Kyung Sun
Kim, Chan Yun
Park, Tae Kwann
author_facet Lee, Si Hyung
Shim, Kyung Sun
Kim, Chan Yun
Park, Tae Kwann
author_sort Lee, Si Hyung
collection PubMed
description Autophagy is an essential cellular process for the degradation and recycling of cellular components, and its dysregulation has been linked to neuronal cell death and neurodegeneration. In glaucoma, the role of autophagy in retinal ganglion cell (RGC) survival remains contradictory. Moreover, the effects of autophagy modulation at different time-points on RGC survival in a glaucoma model have not been investigated. In this study, we assessed the time-dependent role of autophagy in RGC survival in a circumlimbal suture-induced ocular hypertensive (OHT) rat model. Intraocular pressure (IOP) elevation led to a gradual autophagy induction, which reached a maximum between 1 and 4 weeks after OHT induction. On the other hand, early autophagy was impaired between 1 and 3 days after circumlimbal suturing, indicated by increased p62 levels due to reduced autophagosomal turnover. The intravitreal administration of rapamycin at different time-points after the application of the circumlimbal suture indicated that autophagy induction early during OHT development had potent survival-promoting effects in RGCs. In conclusion, our findings suggest that the role of autophagy in RGCs during OHT development might differ in a time-dependent manner. Modulating autophagy at the appropriate time might serve as a potential therapeutic approach to enhance RGC survival in OHT.
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spelling pubmed-79525722021-03-12 Characterization of the role of autophagy in retinal ganglion cell survival over time using a rat model of chronic ocular hypertension Lee, Si Hyung Shim, Kyung Sun Kim, Chan Yun Park, Tae Kwann Sci Rep Article Autophagy is an essential cellular process for the degradation and recycling of cellular components, and its dysregulation has been linked to neuronal cell death and neurodegeneration. In glaucoma, the role of autophagy in retinal ganglion cell (RGC) survival remains contradictory. Moreover, the effects of autophagy modulation at different time-points on RGC survival in a glaucoma model have not been investigated. In this study, we assessed the time-dependent role of autophagy in RGC survival in a circumlimbal suture-induced ocular hypertensive (OHT) rat model. Intraocular pressure (IOP) elevation led to a gradual autophagy induction, which reached a maximum between 1 and 4 weeks after OHT induction. On the other hand, early autophagy was impaired between 1 and 3 days after circumlimbal suturing, indicated by increased p62 levels due to reduced autophagosomal turnover. The intravitreal administration of rapamycin at different time-points after the application of the circumlimbal suture indicated that autophagy induction early during OHT development had potent survival-promoting effects in RGCs. In conclusion, our findings suggest that the role of autophagy in RGCs during OHT development might differ in a time-dependent manner. Modulating autophagy at the appropriate time might serve as a potential therapeutic approach to enhance RGC survival in OHT. Nature Publishing Group UK 2021-03-11 /pmc/articles/PMC7952572/ /pubmed/33707562 http://dx.doi.org/10.1038/s41598-021-85181-x Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lee, Si Hyung
Shim, Kyung Sun
Kim, Chan Yun
Park, Tae Kwann
Characterization of the role of autophagy in retinal ganglion cell survival over time using a rat model of chronic ocular hypertension
title Characterization of the role of autophagy in retinal ganglion cell survival over time using a rat model of chronic ocular hypertension
title_full Characterization of the role of autophagy in retinal ganglion cell survival over time using a rat model of chronic ocular hypertension
title_fullStr Characterization of the role of autophagy in retinal ganglion cell survival over time using a rat model of chronic ocular hypertension
title_full_unstemmed Characterization of the role of autophagy in retinal ganglion cell survival over time using a rat model of chronic ocular hypertension
title_short Characterization of the role of autophagy in retinal ganglion cell survival over time using a rat model of chronic ocular hypertension
title_sort characterization of the role of autophagy in retinal ganglion cell survival over time using a rat model of chronic ocular hypertension
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952572/
https://www.ncbi.nlm.nih.gov/pubmed/33707562
http://dx.doi.org/10.1038/s41598-021-85181-x
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