Sulforaphane Enhances the Ability of Human Retinal Pigment Epithelial Cell against Oxidative Stress, and Its Effect on Gene Expression Profile Evaluated by Microarray Analysis
To gain further insights into the molecular basis of Sulforaphane (SF) mediated retinal pigment epithelial (RPE) 19 cell against oxidative stress, we investigated the effects of SF on the regulation of gene expression on a global scale and tested whether SF can endow RPE cells with the ability to re...
Main Authors: | , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2013-01-01
|
Series: | Oxidative Medicine and Cellular Longevity |
Online Access: | http://dx.doi.org/10.1155/2013/413024 |
id |
doaj-a69554d48be6426296fbb1c9b8c22510 |
---|---|
record_format |
Article |
spelling |
doaj-a69554d48be6426296fbb1c9b8c225102020-11-25T00:36:37ZengHindawi LimitedOxidative Medicine and Cellular Longevity1942-09001942-09942013-01-01201310.1155/2013/413024413024Sulforaphane Enhances the Ability of Human Retinal Pigment Epithelial Cell against Oxidative Stress, and Its Effect on Gene Expression Profile Evaluated by Microarray AnalysisLiang Ye0Ting Yu1Yanqun Li2Bingni Chen3Jinshun Zhang4Zhongyang Wen5Bo Zhang6Xiaohong Zhou7Xiaoqing Li8Feng Li9Wei Cao10Zhong Huang11Institute of Biotherapy, Shenzhen University School of Medicine, Nanhai Ave 3688, Shenzhen, Guangdong 518060, ChinaInstitute of Biotherapy, Shenzhen University School of Medicine, Nanhai Ave 3688, Shenzhen, Guangdong 518060, ChinaInstitute of Biotherapy, Shenzhen University School of Medicine, Nanhai Ave 3688, Shenzhen, Guangdong 518060, ChinaInstitute of Biotherapy, Shenzhen University School of Medicine, Nanhai Ave 3688, Shenzhen, Guangdong 518060, ChinaInstitute of Biotherapy, Shenzhen University School of Medicine, Nanhai Ave 3688, Shenzhen, Guangdong 518060, ChinaInstitute of Biotherapy, Shenzhen University School of Medicine, Nanhai Ave 3688, Shenzhen, Guangdong 518060, ChinaInstitute of Biotherapy, Shenzhen University School of Medicine, Nanhai Ave 3688, Shenzhen, Guangdong 518060, ChinaDepartment of Ophthalmology, Dean A. McGee Eye Institute, University of Oklahoma Health Sciences Center, 608 Stanton L. Young Blvd., Oklahoma City, OK 73104, USAInstitute of Biotherapy, Shenzhen University School of Medicine, Nanhai Ave 3688, Shenzhen, Guangdong 518060, ChinaDepartment of Ophthalmology, Dean A. McGee Eye Institute, University of Oklahoma Health Sciences Center, 608 Stanton L. Young Blvd., Oklahoma City, OK 73104, USADepartment of Ophthalmology, Dean A. McGee Eye Institute, University of Oklahoma Health Sciences Center, 608 Stanton L. Young Blvd., Oklahoma City, OK 73104, USAInstitute of Biotherapy, Shenzhen University School of Medicine, Nanhai Ave 3688, Shenzhen, Guangdong 518060, ChinaTo gain further insights into the molecular basis of Sulforaphane (SF) mediated retinal pigment epithelial (RPE) 19 cell against oxidative stress, we investigated the effects of SF on the regulation of gene expression on a global scale and tested whether SF can endow RPE cells with the ability to resist apoptosis. The data revealed that after exposure to H2O2, RPE 19 cell viability was increased in the cells pretreated with SF compared to the cell not treated with SF. Microarray analysis revealed significant changes in the expression of 69 genes in RPE 19 cells after 6 hours of SF treatment. Based on the functional relevance, eight of the SF-responsive genes, that belong to antioxidant redox system, and inflammatory responsive factors were validated. The up-regulating translation of thioredoxin-1 (Trx1) and the nuclear translocation of Nuclear factor-like2 (Nrf2) were demonstrated by immunoblot analysis in SF treated RPE cells. Our data indicate that SF increases the ability of RPE 19 cell against oxidative stress through up-regulating antioxidative enzymes and down-regulating inflammatory mediators and chemokines. The results suggest that the antioxidant, SF, may be a valuable supplement for preventing and retarding the development of Age Related Macular Degeneration.http://dx.doi.org/10.1155/2013/413024 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Liang Ye Ting Yu Yanqun Li Bingni Chen Jinshun Zhang Zhongyang Wen Bo Zhang Xiaohong Zhou Xiaoqing Li Feng Li Wei Cao Zhong Huang |
spellingShingle |
Liang Ye Ting Yu Yanqun Li Bingni Chen Jinshun Zhang Zhongyang Wen Bo Zhang Xiaohong Zhou Xiaoqing Li Feng Li Wei Cao Zhong Huang Sulforaphane Enhances the Ability of Human Retinal Pigment Epithelial Cell against Oxidative Stress, and Its Effect on Gene Expression Profile Evaluated by Microarray Analysis Oxidative Medicine and Cellular Longevity |
author_facet |
Liang Ye Ting Yu Yanqun Li Bingni Chen Jinshun Zhang Zhongyang Wen Bo Zhang Xiaohong Zhou Xiaoqing Li Feng Li Wei Cao Zhong Huang |
author_sort |
Liang Ye |
title |
Sulforaphane Enhances the Ability of Human Retinal Pigment Epithelial Cell against Oxidative Stress, and Its Effect on Gene Expression Profile Evaluated by Microarray Analysis |
title_short |
Sulforaphane Enhances the Ability of Human Retinal Pigment Epithelial Cell against Oxidative Stress, and Its Effect on Gene Expression Profile Evaluated by Microarray Analysis |
title_full |
Sulforaphane Enhances the Ability of Human Retinal Pigment Epithelial Cell against Oxidative Stress, and Its Effect on Gene Expression Profile Evaluated by Microarray Analysis |
title_fullStr |
Sulforaphane Enhances the Ability of Human Retinal Pigment Epithelial Cell against Oxidative Stress, and Its Effect on Gene Expression Profile Evaluated by Microarray Analysis |
title_full_unstemmed |
Sulforaphane Enhances the Ability of Human Retinal Pigment Epithelial Cell against Oxidative Stress, and Its Effect on Gene Expression Profile Evaluated by Microarray Analysis |
title_sort |
sulforaphane enhances the ability of human retinal pigment epithelial cell against oxidative stress, and its effect on gene expression profile evaluated by microarray analysis |
publisher |
Hindawi Limited |
series |
Oxidative Medicine and Cellular Longevity |
issn |
1942-0900 1942-0994 |
publishDate |
2013-01-01 |
description |
To gain further insights into the molecular basis of Sulforaphane (SF) mediated retinal pigment epithelial (RPE) 19 cell against oxidative stress, we investigated the effects of SF on the regulation of gene expression on a global scale and tested whether SF can endow RPE cells with the ability to resist apoptosis. The data revealed that after exposure to H2O2, RPE 19 cell viability was increased in the cells pretreated with SF compared to the cell not treated with SF. Microarray analysis revealed significant changes in the expression of 69 genes in RPE 19 cells after 6 hours of SF treatment. Based on the functional relevance, eight of the SF-responsive genes, that belong to antioxidant redox system, and inflammatory responsive factors were validated. The up-regulating translation of thioredoxin-1 (Trx1) and the nuclear translocation of Nuclear factor-like2 (Nrf2) were demonstrated by immunoblot analysis in SF treated RPE cells. Our data indicate that SF increases the ability of RPE 19 cell against oxidative stress through up-regulating antioxidative enzymes and down-regulating inflammatory mediators and chemokines. The results suggest that the antioxidant, SF, may be a valuable supplement for preventing and retarding the development of Age Related Macular Degeneration. |
url |
http://dx.doi.org/10.1155/2013/413024 |
work_keys_str_mv |
AT liangye sulforaphaneenhancestheabilityofhumanretinalpigmentepithelialcellagainstoxidativestressanditseffectongeneexpressionprofileevaluatedbymicroarrayanalysis AT tingyu sulforaphaneenhancestheabilityofhumanretinalpigmentepithelialcellagainstoxidativestressanditseffectongeneexpressionprofileevaluatedbymicroarrayanalysis AT yanqunli sulforaphaneenhancestheabilityofhumanretinalpigmentepithelialcellagainstoxidativestressanditseffectongeneexpressionprofileevaluatedbymicroarrayanalysis AT bingnichen sulforaphaneenhancestheabilityofhumanretinalpigmentepithelialcellagainstoxidativestressanditseffectongeneexpressionprofileevaluatedbymicroarrayanalysis AT jinshunzhang sulforaphaneenhancestheabilityofhumanretinalpigmentepithelialcellagainstoxidativestressanditseffectongeneexpressionprofileevaluatedbymicroarrayanalysis AT zhongyangwen sulforaphaneenhancestheabilityofhumanretinalpigmentepithelialcellagainstoxidativestressanditseffectongeneexpressionprofileevaluatedbymicroarrayanalysis AT bozhang sulforaphaneenhancestheabilityofhumanretinalpigmentepithelialcellagainstoxidativestressanditseffectongeneexpressionprofileevaluatedbymicroarrayanalysis AT xiaohongzhou sulforaphaneenhancestheabilityofhumanretinalpigmentepithelialcellagainstoxidativestressanditseffectongeneexpressionprofileevaluatedbymicroarrayanalysis AT xiaoqingli sulforaphaneenhancestheabilityofhumanretinalpigmentepithelialcellagainstoxidativestressanditseffectongeneexpressionprofileevaluatedbymicroarrayanalysis AT fengli sulforaphaneenhancestheabilityofhumanretinalpigmentepithelialcellagainstoxidativestressanditseffectongeneexpressionprofileevaluatedbymicroarrayanalysis AT weicao sulforaphaneenhancestheabilityofhumanretinalpigmentepithelialcellagainstoxidativestressanditseffectongeneexpressionprofileevaluatedbymicroarrayanalysis AT zhonghuang sulforaphaneenhancestheabilityofhumanretinalpigmentepithelialcellagainstoxidativestressanditseffectongeneexpressionprofileevaluatedbymicroarrayanalysis |
_version_ |
1725304528102752256 |