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...

Full description

Bibliographic Details
Main Authors: Yanru He, Si Pang, Jia Huang, Kongbo Zhu, Jiayi Tong, Yaoliang Tang, Genshan Ma, Lijuan Chen
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2018/5207031
id doaj-5b2cbaa02df14e16b0e392ebd71df996
record_format Article
spelling 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
work_keys_str_mv AT yanruhe blockadeofrbpjmediatednotchsignalingpathwayexacerbatescardiacremodelingafterinfarctionbyincreasingapoptosisinmice
AT sipang blockadeofrbpjmediatednotchsignalingpathwayexacerbatescardiacremodelingafterinfarctionbyincreasingapoptosisinmice
AT jiahuang blockadeofrbpjmediatednotchsignalingpathwayexacerbatescardiacremodelingafterinfarctionbyincreasingapoptosisinmice
AT kongbozhu blockadeofrbpjmediatednotchsignalingpathwayexacerbatescardiacremodelingafterinfarctionbyincreasingapoptosisinmice
AT jiayitong blockadeofrbpjmediatednotchsignalingpathwayexacerbatescardiacremodelingafterinfarctionbyincreasingapoptosisinmice
AT yaoliangtang blockadeofrbpjmediatednotchsignalingpathwayexacerbatescardiacremodelingafterinfarctionbyincreasingapoptosisinmice
AT genshanma blockadeofrbpjmediatednotchsignalingpathwayexacerbatescardiacremodelingafterinfarctionbyincreasingapoptosisinmice
AT lijuanchen blockadeofrbpjmediatednotchsignalingpathwayexacerbatescardiacremodelingafterinfarctionbyincreasingapoptosisinmice
_version_ 1725739406681178112