{"title":"miR-204靶向SIRT1调控人晶状体上皮细胞凋亡的机制","authors":"Xiao-Liang Xie, Jiangyue Zhao, Fangkun Zhao, Yu Qin","doi":"10.3760/CMA.J.ISSN.1006-4443.2017.05.022","DOIUrl":null,"url":null,"abstract":"Objective \nTo investigate the effect of miR-204 expression on apoptosis of human lens epithelial cell line (LECs) SRA01/04 in vitro and the mechanism of targeting SIRT1. \n \n \nMethods \nHydrogen peroxide (H2O2) was used to construct the cell apoptosis model of human lens epithelial cell line SRA01/04 in vitro. MiR-204 mimic and inhibitor were transiently transfected into SRA01/04 cells using Lipofectamine 2000 to regulate the expression level of miR-204. Flow cytometry was used to detect the cell apoptosis rate in each group SRA01/04 cells. By microRNA databases and recent study researches, we predicted that SIRT1 maybe a potential target gene of miR-204. Quantitative real-time PCR (qRT-PCR) were used to detect the expression level of miR-204 and SIRT1 gene. \n \n \nResults \nQuantitative real-time PCR results showed that the expression level of miR-204 in cell apoptosis model of SRA01/04 was significantly higher than the normal SRA01/04 cells. Overexpression of miR-204 in SRA01/04 promoted H2O2-induced cell apoptosis, and down-regulated the expression level of SIRT1 gene. While downexpression of miR-204 in SRA01/04 reduced H2O2-induced cell apoptosis, and up-regulated the expression level of SIRT1 gene. Each result was statistically significant (P <0.01). \n \n \nConclusions \nThe expression level of miR-204 in cell apoptosis model of SRA01/04 is significantly higher than the normal SRA01/04 cells. MiR-204 can regulate the apoptosis of the human lens epithelial cells by targeting SIRT1 gene. Thus, miR-204 may play an important role in the pathogenesis of caracts with lens epithelial cell apoptosis. \n \n \nKey words: \nmiR-204; SIRT1; Cell apoptosis; Cataract","PeriodicalId":10236,"journal":{"name":"中国实用眼科杂志","volume":"27 1","pages":"527-532"},"PeriodicalIF":0.0000,"publicationDate":"2017-05-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Regulation mechanism of miR-204 targeted SIRT1 in human lens epithelial cell apoptosis\",\"authors\":\"Xiao-Liang Xie, Jiangyue Zhao, Fangkun Zhao, Yu Qin\",\"doi\":\"10.3760/CMA.J.ISSN.1006-4443.2017.05.022\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective \\nTo investigate the effect of miR-204 expression on apoptosis of human lens epithelial cell line (LECs) SRA01/04 in vitro and the mechanism of targeting SIRT1. \\n \\n \\nMethods \\nHydrogen peroxide (H2O2) was used to construct the cell apoptosis model of human lens epithelial cell line SRA01/04 in vitro. MiR-204 mimic and inhibitor were transiently transfected into SRA01/04 cells using Lipofectamine 2000 to regulate the expression level of miR-204. Flow cytometry was used to detect the cell apoptosis rate in each group SRA01/04 cells. By microRNA databases and recent study researches, we predicted that SIRT1 maybe a potential target gene of miR-204. Quantitative real-time PCR (qRT-PCR) were used to detect the expression level of miR-204 and SIRT1 gene. \\n \\n \\nResults \\nQuantitative real-time PCR results showed that the expression level of miR-204 in cell apoptosis model of SRA01/04 was significantly higher than the normal SRA01/04 cells. Overexpression of miR-204 in SRA01/04 promoted H2O2-induced cell apoptosis, and down-regulated the expression level of SIRT1 gene. While downexpression of miR-204 in SRA01/04 reduced H2O2-induced cell apoptosis, and up-regulated the expression level of SIRT1 gene. Each result was statistically significant (P <0.01). \\n \\n \\nConclusions \\nThe expression level of miR-204 in cell apoptosis model of SRA01/04 is significantly higher than the normal SRA01/04 cells. MiR-204 can regulate the apoptosis of the human lens epithelial cells by targeting SIRT1 gene. Thus, miR-204 may play an important role in the pathogenesis of caracts with lens epithelial cell apoptosis. \\n \\n \\nKey words: \\nmiR-204; SIRT1; Cell apoptosis; Cataract\",\"PeriodicalId\":10236,\"journal\":{\"name\":\"中国实用眼科杂志\",\"volume\":\"27 1\",\"pages\":\"527-532\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-05-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"中国实用眼科杂志\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3760/CMA.J.ISSN.1006-4443.2017.05.022\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"中国实用眼科杂志","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3760/CMA.J.ISSN.1006-4443.2017.05.022","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Regulation mechanism of miR-204 targeted SIRT1 in human lens epithelial cell apoptosis
Objective
To investigate the effect of miR-204 expression on apoptosis of human lens epithelial cell line (LECs) SRA01/04 in vitro and the mechanism of targeting SIRT1.
Methods
Hydrogen peroxide (H2O2) was used to construct the cell apoptosis model of human lens epithelial cell line SRA01/04 in vitro. MiR-204 mimic and inhibitor were transiently transfected into SRA01/04 cells using Lipofectamine 2000 to regulate the expression level of miR-204. Flow cytometry was used to detect the cell apoptosis rate in each group SRA01/04 cells. By microRNA databases and recent study researches, we predicted that SIRT1 maybe a potential target gene of miR-204. Quantitative real-time PCR (qRT-PCR) were used to detect the expression level of miR-204 and SIRT1 gene.
Results
Quantitative real-time PCR results showed that the expression level of miR-204 in cell apoptosis model of SRA01/04 was significantly higher than the normal SRA01/04 cells. Overexpression of miR-204 in SRA01/04 promoted H2O2-induced cell apoptosis, and down-regulated the expression level of SIRT1 gene. While downexpression of miR-204 in SRA01/04 reduced H2O2-induced cell apoptosis, and up-regulated the expression level of SIRT1 gene. Each result was statistically significant (P <0.01).
Conclusions
The expression level of miR-204 in cell apoptosis model of SRA01/04 is significantly higher than the normal SRA01/04 cells. MiR-204 can regulate the apoptosis of the human lens epithelial cells by targeting SIRT1 gene. Thus, miR-204 may play an important role in the pathogenesis of caracts with lens epithelial cell apoptosis.
Key words:
miR-204; SIRT1; Cell apoptosis; Cataract
期刊介绍:
China Practical Ophthalmology was founded in May 1983. It is supervised by the National Health Commission of the People's Republic of China, sponsored by the Chinese Medical Association and China Medical University, and publicly distributed at home and abroad. It is a national-level excellent core academic journal of comprehensive ophthalmology and a series of journals of the Chinese Medical Association.
China Practical Ophthalmology aims to guide and improve the theoretical level and actual clinical diagnosis and treatment ability of frontline ophthalmologists in my country. It is characterized by close integration with clinical practice, and timely publishes academic articles and scientific research results with high practical value to clinicians, so that readers can understand and use them, improve the theoretical level and diagnosis and treatment ability of ophthalmologists, help and support their innovative development, and is deeply welcomed and loved by ophthalmologists and readers.