Blockade of RBP-J-Mediated Notch Signaling Pathway Exacerbates Cardiac Remodeling after Infarction by Increasing Apoptosis in Mice
Background. Ischemic heart disease (IHD) is the major cause of death in patients with cardiovascular disease. Cardiac remodeling is a common pathological change following myocardial infarction (MI), and cardiomyocyte apoptosis plays a key role in this change. Transcription factor recombination signa...
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doaj-5b2cbaa02df14e16b0e392ebd71df9962020-11-24T22:30:47ZengHindawi LimitedBioMed Research International2314-61332314-61412018-01-01201810.1155/2018/52070315207031Blockade of RBP-J-Mediated Notch Signaling Pathway Exacerbates Cardiac Remodeling after Infarction by Increasing Apoptosis in MiceYanru He0Si Pang1Jia Huang2Kongbo Zhu3Jiayi Tong4Yaoliang Tang5Genshan Ma6Lijuan Chen7Department of Cardiology, Zhongda Hospital Affiliated to Southeast University, Nanjing, ChinaDepartment of Cardiology, Zhongda Hospital Affiliated to Southeast University, Nanjing, ChinaDepartment of Cardiology, Zhongda Hospital Affiliated to Southeast University, Nanjing, ChinaDepartment of Cardiology, Zhongda Hospital Affiliated to Southeast University, Nanjing, ChinaDepartment of Cardiology, Zhongda Hospital Affiliated to Southeast University, Nanjing, ChinaDepartment of Cardiovascular Medicine, Georgia Regents University, USADepartment of Cardiology, Zhongda Hospital Affiliated to Southeast University, Nanjing, ChinaDepartment of Cardiology, Zhongda Hospital Affiliated to Southeast University, Nanjing, ChinaBackground. Ischemic heart disease (IHD) is the major cause of death in patients with cardiovascular disease. Cardiac remodeling is a common pathological change following myocardial infarction (MI), and cardiomyocyte apoptosis plays a key role in this change. Transcription factor recombination signal-binding protein-J (RBP-J)-mediated Notch signaling pathway has been implicated in several inherited cardiovascular diseases, including aortic valve diseases, but whether the RBP-J-mediated Notch signaling pathway plays a role in cardiomyocyte apoptosis after MI is unclear. Method. We crossed RBP-Jfl/fl mice and Myh6-Cre/Esr1 transgenic mice to delete RBP-J in vivo and to partly inhibit the canonical Notch signaling pathway. MI was induced in mice by permanent ligation of the left anterior descending coronary artery followed by the knockout of RBP-J. Cardiac function and morphology were assessed by echocardiography and histological analysis 4 weeks after infarction. In addition, the expression and regulation of apoptosis-related molecules were examined by real time PCR and western blot. Results. RBP-J knockout decreased the survival rate and deteriorated post-MI remodeling and function in mice, and this effect was associated with increased cardiomyocyte apoptosis. The potential mechanisms might be related to the downregulated expression of bcl-2, upregulated expression of bax, and cleaved-caspase 3 to exacerbate cardiomyocyte apoptosis. Conclusion. These findings show that the RBP-J-mediated Notch signaling pathway in cardiomyocytes limits ventricular remodeling and improves cardiac function after MI. The RBP-J-mediated Notch signaling pathway has a protective role in cardiomyocyte apoptosis following cardiac injury.http://dx.doi.org/10.1155/2018/5207031 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yanru He Si Pang Jia Huang Kongbo Zhu Jiayi Tong Yaoliang Tang Genshan Ma Lijuan Chen |
spellingShingle |
Yanru He Si Pang Jia Huang Kongbo Zhu Jiayi Tong Yaoliang Tang Genshan Ma Lijuan Chen Blockade of RBP-J-Mediated Notch Signaling Pathway Exacerbates Cardiac Remodeling after Infarction by Increasing Apoptosis in Mice BioMed Research International |
author_facet |
Yanru He Si Pang Jia Huang Kongbo Zhu Jiayi Tong Yaoliang Tang Genshan Ma Lijuan Chen |
author_sort |
Yanru He |
title |
Blockade of RBP-J-Mediated Notch Signaling Pathway Exacerbates Cardiac Remodeling after Infarction by Increasing Apoptosis in Mice |
title_short |
Blockade of RBP-J-Mediated Notch Signaling Pathway Exacerbates Cardiac Remodeling after Infarction by Increasing Apoptosis in Mice |
title_full |
Blockade of RBP-J-Mediated Notch Signaling Pathway Exacerbates Cardiac Remodeling after Infarction by Increasing Apoptosis in Mice |
title_fullStr |
Blockade of RBP-J-Mediated Notch Signaling Pathway Exacerbates Cardiac Remodeling after Infarction by Increasing Apoptosis in Mice |
title_full_unstemmed |
Blockade of RBP-J-Mediated Notch Signaling Pathway Exacerbates Cardiac Remodeling after Infarction by Increasing Apoptosis in Mice |
title_sort |
blockade of rbp-j-mediated notch signaling pathway exacerbates cardiac remodeling after infarction by increasing apoptosis in mice |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6133 2314-6141 |
publishDate |
2018-01-01 |
description |
Background. Ischemic heart disease (IHD) is the major cause of death in patients with cardiovascular disease. Cardiac remodeling is a common pathological change following myocardial infarction (MI), and cardiomyocyte apoptosis plays a key role in this change. Transcription factor recombination signal-binding protein-J (RBP-J)-mediated Notch signaling pathway has been implicated in several inherited cardiovascular diseases, including aortic valve diseases, but whether the RBP-J-mediated Notch signaling pathway plays a role in cardiomyocyte apoptosis after MI is unclear. Method. We crossed RBP-Jfl/fl mice and Myh6-Cre/Esr1 transgenic mice to delete RBP-J in vivo and to partly inhibit the canonical Notch signaling pathway. MI was induced in mice by permanent ligation of the left anterior descending coronary artery followed by the knockout of RBP-J. Cardiac function and morphology were assessed by echocardiography and histological analysis 4 weeks after infarction. In addition, the expression and regulation of apoptosis-related molecules were examined by real time PCR and western blot. Results. RBP-J knockout decreased the survival rate and deteriorated post-MI remodeling and function in mice, and this effect was associated with increased cardiomyocyte apoptosis. The potential mechanisms might be related to the downregulated expression of bcl-2, upregulated expression of bax, and cleaved-caspase 3 to exacerbate cardiomyocyte apoptosis. Conclusion. These findings show that the RBP-J-mediated Notch signaling pathway in cardiomyocytes limits ventricular remodeling and improves cardiac function after MI. The RBP-J-mediated Notch signaling pathway has a protective role in cardiomyocyte apoptosis following cardiac injury. |
url |
http://dx.doi.org/10.1155/2018/5207031 |
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