MicroRNA-214 Protects Cardiac Myocytes Against H2O2-Induced Injury
ABSTRACT Reactive oxygen species (ROS)‐induced cardiac myocyte injury resulting from changes in the expression levels of multiple genes plays a critical role in the pathogenesis of numerous heart diseases. The purpose of this study was to determine the potential roles of microRNA‐214 (miR‐214) in hy...
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Published in | Journal of cellular biochemistry Vol. 115; no. 1; pp. 93 - 101 |
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Main Authors | , , , , , |
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Language | English |
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01.01.2014
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Abstract | ABSTRACT
Reactive oxygen species (ROS)‐induced cardiac myocyte injury resulting from changes in the expression levels of multiple genes plays a critical role in the pathogenesis of numerous heart diseases. The purpose of this study was to determine the potential roles of microRNA‐214 (miR‐214) in hydrogen peroxide (H2O2)‐mediated gene regulation in cardiac myocytes. In this study, we used quantitative real‐time RT‐PCR (qRT‐PCR) to demonstrate that miR‐214 was upregulated in cardiac myocytes after treatment with H2O2. We transfected cells with pre‐miR‐214 to upregulate miR‐214 expression and transfected cells with a miR‐214 inhibitor (anti‐miR‐214) to downregulate miR‐214 expression. H2O2‐induced cardiac cell apoptosis was detected by flow cytometry. The level of apoptosis was increased by the miR‐214 inhibitor and decreased by pre‐miR‐214. Therefore, we believe that miR‐214 plays a positive role in H2O2‐induced cardiac cell apoptosis. Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) is constitutively active and is considered to be the primary downregulator of the pro‐oncogenic PI3K/Akt pathway. Western blot analysis revealed that the expression of the PTEN protein in cardiac myocytes decreased after H2O2 induction. Anti‐miR‐214 increased PTEN protein expression level, in contrast, pre‐miR‐214 decreased the PTEN protein expression level in cultured cardiac myocytes. These results indicate that PTEN is regulated by miR‐214 and serves as an important target of miR‐214 in cardiac myocytes. In conclusion, miR‐214 is sensitive to H2O2 stimulation, and miR‐214 protects cardiac myocytes against H2O2‐induced injury via one of its targets, PTEN. J. Cell. Biochem. 115: 93–101, 2014. © 2013 Wiley Periodicals, Inc. |
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AbstractList | ABSTRACT
Reactive oxygen species (ROS)‐induced cardiac myocyte injury resulting from changes in the expression levels of multiple genes plays a critical role in the pathogenesis of numerous heart diseases. The purpose of this study was to determine the potential roles of microRNA‐214 (miR‐214) in hydrogen peroxide (H2O2)‐mediated gene regulation in cardiac myocytes. In this study, we used quantitative real‐time RT‐PCR (qRT‐PCR) to demonstrate that miR‐214 was upregulated in cardiac myocytes after treatment with H2O2. We transfected cells with pre‐miR‐214 to upregulate miR‐214 expression and transfected cells with a miR‐214 inhibitor (anti‐miR‐214) to downregulate miR‐214 expression. H2O2‐induced cardiac cell apoptosis was detected by flow cytometry. The level of apoptosis was increased by the miR‐214 inhibitor and decreased by pre‐miR‐214. Therefore, we believe that miR‐214 plays a positive role in H2O2‐induced cardiac cell apoptosis. Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) is constitutively active and is considered to be the primary downregulator of the pro‐oncogenic PI3K/Akt pathway. Western blot analysis revealed that the expression of the PTEN protein in cardiac myocytes decreased after H2O2 induction. Anti‐miR‐214 increased PTEN protein expression level, in contrast, pre‐miR‐214 decreased the PTEN protein expression level in cultured cardiac myocytes. These results indicate that PTEN is regulated by miR‐214 and serves as an important target of miR‐214 in cardiac myocytes. In conclusion, miR‐214 is sensitive to H2O2 stimulation, and miR‐214 protects cardiac myocytes against H2O2‐induced injury via one of its targets, PTEN. J. Cell. Biochem. 115: 93–101, 2014. © 2013 Wiley Periodicals, Inc. Reactive oxygen species (ROS)-induced cardiac myocyte injury resulting from changes in the expression levels of multiple genes plays a critical role in the pathogenesis of numerous heart diseases. The purpose of this study was to determine the potential roles of microRNA-214 (miR-214) in hydrogen peroxide (H2O2)-mediated gene regulation in cardiac myocytes. In this study, we used quantitative real-time RT-PCR (qRT-PCR) to demonstrate that miR-214 was upregulated in cardiac myocytes after treatment with H2O2. We transfected cells with pre-miR-214 to upregulate miR-214 expression and transfected cells with a miR-214 inhibitor (anti-miR-214) to downregulate miR-214 expression. H2O2-induced cardiac cell apoptosis was detected by flow cytometry. The level of apoptosis was increased by the miR-214 inhibitor and decreased by pre-miR-214. Therefore, we believe that miR-214 plays a positive role in H2O2-induced cardiac cell apoptosis. Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) is constitutively active and is considered to be the primary downregulator of the pro-oncogenic PI3K/Akt pathway. Western blot analysis revealed that the expression of the PTEN protein in cardiac myocytes decreased after H2O2 induction. Anti-miR-214 increased PTEN protein expression level, in contrast, pre-miR-214 decreased the PTEN protein expression level in cultured cardiac myocytes. These results indicate that PTEN is regulated by miR-214 and serves as an important target of miR-214 in cardiac myocytes. In conclusion, miR-214 is sensitive to H2O2 stimulation, and miR-214 protects cardiac myocytes against H2O2-induced injury via one of its targets, PTEN. Reactive oxygen species (ROS)-induced cardiac myocyte injury resulting from changes in the expression levels of multiple genes plays a critical role in the pathogenesis of numerous heart diseases. The purpose of this study was to determine the potential roles of microRNA-214 (miR-214) in hydrogen peroxide (H2O2)-mediated gene regulation in cardiac myocytes. In this study, we used quantitative real-time RT-PCR (qRT-PCR) to demonstrate that miR-214 was upregulated in cardiac myocytes after treatment with H2O2. We transfected cells with pre-miR-214 to upregulate miR-214 expression and transfected cells with a miR-214 inhibitor (anti-miR-214) to downregulate miR-214 expression. H2O2-induced cardiac cell apoptosis was detected by flow cytometry. The level of apoptosis was increased by the miR-214 inhibitor and decreased by pre-miR-214. Therefore, we believe that miR-214 plays a positive role in H2O2-induced cardiac cell apoptosis. Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) is constitutively active and is considered to be the primary downregulator of the pro-oncogenic PI3K/Akt pathway. Western blot analysis revealed that the expression of the PTEN protein in cardiac myocytes decreased after H2O2 induction. Anti-miR-214 increased PTEN protein expression level, in contrast, pre-miR-214 decreased the PTEN protein expression level in cultured cardiac myocytes. These results indicate that PTEN is regulated by miR-214 and serves as an important target of miR-214 in cardiac myocytes. In conclusion, miR-214 is sensitive to H2O2 stimulation, and miR-214 protects cardiac myocytes against H2O2-induced injury via one of its targets, PTEN. J. Cell. Biochem. 115: 93-101, 2014. © 2013 Wiley Periodicals, Inc. [PUBLICATION ABSTRACT] |
Author | Dong, Hua Bian, Xiaohua Yang, Xingwei Lv, Guangwei Shao, Suxia Dong, Shimin |
Author_xml | – sequence: 1 givenname: Guangwei surname: Lv fullname: Lv, Guangwei organization: Department of ICU, The Third Hospital of Hebei Medical University, Hebei ProvinceP.R. China, Shijiazhuang City – sequence: 2 givenname: Suxia surname: Shao fullname: Shao, Suxia organization: Department of histology and embryology, Hebei Medical University, Hebei ProvinceP.R. China, Shijiazhuang City – sequence: 3 givenname: Hua surname: Dong fullname: Dong, Hua organization: Department of histology and embryology, Hebei Medical University, Hebei ProvinceP.R. China, Shijiazhuang City – sequence: 4 givenname: Xiaohua surname: Bian fullname: Bian, Xiaohua organization: Department of ICU, The Third Hospital of Hebei Medical University, Hebei ProvinceP.R. China, Shijiazhuang City – sequence: 5 givenname: Xingwei surname: Yang fullname: Yang, Xingwei organization: Department of ICU, The Third Hospital of Hebei Medical University, Hebei ProvinceP.R. China, Shijiazhuang City – sequence: 6 givenname: Shimin surname: Dong fullname: Dong, Shimin email: Correspondence to: Shimin Dong, The Third hospital of Hebei Medical University, Shijiazhuang City, HeBei Province, P.R.China., lvguangweiwei@163.com organization: Department of ICU, The Third Hospital of Hebei Medical University, Hebei ProvinceP.R. China, Shijiazhuang City |
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Keywords | APOPTOSIS MicroRNA-214 PHOSPHATASE AND TENSIN HOMOLOG (PTEN) H2O2 CARDIAC MYOCYTES |
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Reactive oxygen species (ROS)‐induced cardiac myocyte injury resulting from changes in the expression levels of multiple genes plays a critical role... Reactive oxygen species (ROS)-induced cardiac myocyte injury resulting from changes in the expression levels of multiple genes plays a critical role in the... |
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SubjectTerms | Animals APOPTOSIS Apoptosis - drug effects Apoptosis - genetics CARDIAC MYOCYTES Cell Survival - drug effects Cells, Cultured Gene Expression Regulation - drug effects H2O2 Hydrogen Peroxide - pharmacology MicroRNA-214 MicroRNAs - physiology Myocytes, Cardiac - drug effects Myocytes, Cardiac - physiology PHOSPHATASE AND TENSIN HOMOLOG (PTEN) PTEN Phosphohydrolase - genetics PTEN Phosphohydrolase - metabolism Rats Rats, Sprague-Dawley |
Title | MicroRNA-214 Protects Cardiac Myocytes Against H2O2-Induced Injury |
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