Cargando…

Sirtuin 1 Induces Choroidal Neovascularization and Triggers Age-Related Macular Degeneration by Promoting LCN2 through SOX9 Deacetylation

Increasing studies have identified the function of sirtuin-1 (SIRT1) in ocular diseases. Hence, this study is aimed at exploring the potential role of SIRT1 in choroidal neovascularization- (CNV-) induced age-related macular degeneration (AMD) development and the associated mechanism. Expression of...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Su, Huang, Zhi, Jiang, Hao, Xiu, Jiangfan, Zhang, Liying, Long, Qiurong, Yang, Yuhan, Yu, Lu, Lu, Lu, Gu, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203240/
https://www.ncbi.nlm.nih.gov/pubmed/35720180
http://dx.doi.org/10.1155/2022/1671438
_version_ 1784728686202716160
author Zhao, Su
Huang, Zhi
Jiang, Hao
Xiu, Jiangfan
Zhang, Liying
Long, Qiurong
Yang, Yuhan
Yu, Lu
Lu, Lu
Gu, Hao
author_facet Zhao, Su
Huang, Zhi
Jiang, Hao
Xiu, Jiangfan
Zhang, Liying
Long, Qiurong
Yang, Yuhan
Yu, Lu
Lu, Lu
Gu, Hao
author_sort Zhao, Su
collection PubMed
description Increasing studies have identified the function of sirtuin-1 (SIRT1) in ocular diseases. Hence, this study is aimed at exploring the potential role of SIRT1 in choroidal neovascularization- (CNV-) induced age-related macular degeneration (AMD) development and the associated mechanism. Expression of SIRT1/SOX9/LCN2 in the hypoxic cells was determined, and their interactions were predicted by bioinformatics websites and followed by the verification by luciferase assay and chromatin immunoprecipitation (ChIP). Their in vitro effects on hypoxic cells concerning cell viability, apoptosis, migration, and angiogenesis were detected through gain- and loss-of-function assays. Besides, their in vivo effect was explored using the established CNV mouse models. Highly expressed LCN2, SOX9, and SIRT1 were observed in hypoxic cells. LCN2 was increased by SOX9 and SIRT1 deacetylated SOX9 to promote its nuclear translocation, which further inhibited the viability of human retinal pigment epithelial cells and promoted cell apoptosis and angiogenesis as well as CNV-induced AMD formation. The relieving role of LCN2 inhibition on CNV-induced AMD without toxicity for mice was also demonstrated by in vivo experiments. Overall, SIRT1 promoted the formation of CNV-induced AMD through SOX9 deacetylation-caused LCN2 upregulation, representing a promising target for CNV-induced AMD management.
format Online
Article
Text
id pubmed-9203240
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-92032402022-06-17 Sirtuin 1 Induces Choroidal Neovascularization and Triggers Age-Related Macular Degeneration by Promoting LCN2 through SOX9 Deacetylation Zhao, Su Huang, Zhi Jiang, Hao Xiu, Jiangfan Zhang, Liying Long, Qiurong Yang, Yuhan Yu, Lu Lu, Lu Gu, Hao Oxid Med Cell Longev Research Article Increasing studies have identified the function of sirtuin-1 (SIRT1) in ocular diseases. Hence, this study is aimed at exploring the potential role of SIRT1 in choroidal neovascularization- (CNV-) induced age-related macular degeneration (AMD) development and the associated mechanism. Expression of SIRT1/SOX9/LCN2 in the hypoxic cells was determined, and their interactions were predicted by bioinformatics websites and followed by the verification by luciferase assay and chromatin immunoprecipitation (ChIP). Their in vitro effects on hypoxic cells concerning cell viability, apoptosis, migration, and angiogenesis were detected through gain- and loss-of-function assays. Besides, their in vivo effect was explored using the established CNV mouse models. Highly expressed LCN2, SOX9, and SIRT1 were observed in hypoxic cells. LCN2 was increased by SOX9 and SIRT1 deacetylated SOX9 to promote its nuclear translocation, which further inhibited the viability of human retinal pigment epithelial cells and promoted cell apoptosis and angiogenesis as well as CNV-induced AMD formation. The relieving role of LCN2 inhibition on CNV-induced AMD without toxicity for mice was also demonstrated by in vivo experiments. Overall, SIRT1 promoted the formation of CNV-induced AMD through SOX9 deacetylation-caused LCN2 upregulation, representing a promising target for CNV-induced AMD management. Hindawi 2022-06-09 /pmc/articles/PMC9203240/ /pubmed/35720180 http://dx.doi.org/10.1155/2022/1671438 Text en Copyright © 2022 Su Zhao et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhao, Su
Huang, Zhi
Jiang, Hao
Xiu, Jiangfan
Zhang, Liying
Long, Qiurong
Yang, Yuhan
Yu, Lu
Lu, Lu
Gu, Hao
Sirtuin 1 Induces Choroidal Neovascularization and Triggers Age-Related Macular Degeneration by Promoting LCN2 through SOX9 Deacetylation
title Sirtuin 1 Induces Choroidal Neovascularization and Triggers Age-Related Macular Degeneration by Promoting LCN2 through SOX9 Deacetylation
title_full Sirtuin 1 Induces Choroidal Neovascularization and Triggers Age-Related Macular Degeneration by Promoting LCN2 through SOX9 Deacetylation
title_fullStr Sirtuin 1 Induces Choroidal Neovascularization and Triggers Age-Related Macular Degeneration by Promoting LCN2 through SOX9 Deacetylation
title_full_unstemmed Sirtuin 1 Induces Choroidal Neovascularization and Triggers Age-Related Macular Degeneration by Promoting LCN2 through SOX9 Deacetylation
title_short Sirtuin 1 Induces Choroidal Neovascularization and Triggers Age-Related Macular Degeneration by Promoting LCN2 through SOX9 Deacetylation
title_sort sirtuin 1 induces choroidal neovascularization and triggers age-related macular degeneration by promoting lcn2 through sox9 deacetylation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203240/
https://www.ncbi.nlm.nih.gov/pubmed/35720180
http://dx.doi.org/10.1155/2022/1671438
work_keys_str_mv AT zhaosu sirtuin1induceschoroidalneovascularizationandtriggersagerelatedmaculardegenerationbypromotinglcn2throughsox9deacetylation
AT huangzhi sirtuin1induceschoroidalneovascularizationandtriggersagerelatedmaculardegenerationbypromotinglcn2throughsox9deacetylation
AT jianghao sirtuin1induceschoroidalneovascularizationandtriggersagerelatedmaculardegenerationbypromotinglcn2throughsox9deacetylation
AT xiujiangfan sirtuin1induceschoroidalneovascularizationandtriggersagerelatedmaculardegenerationbypromotinglcn2throughsox9deacetylation
AT zhangliying sirtuin1induceschoroidalneovascularizationandtriggersagerelatedmaculardegenerationbypromotinglcn2throughsox9deacetylation
AT longqiurong sirtuin1induceschoroidalneovascularizationandtriggersagerelatedmaculardegenerationbypromotinglcn2throughsox9deacetylation
AT yangyuhan sirtuin1induceschoroidalneovascularizationandtriggersagerelatedmaculardegenerationbypromotinglcn2throughsox9deacetylation
AT yulu sirtuin1induceschoroidalneovascularizationandtriggersagerelatedmaculardegenerationbypromotinglcn2throughsox9deacetylation
AT lulu sirtuin1induceschoroidalneovascularizationandtriggersagerelatedmaculardegenerationbypromotinglcn2throughsox9deacetylation
AT guhao sirtuin1induceschoroidalneovascularizationandtriggersagerelatedmaculardegenerationbypromotinglcn2throughsox9deacetylation