Aerobic training attenuates cardiac remodeling in mice post-myocardial infarction by inhibiting the p300/CBP-associated factor

被引:1
作者
Huang, Chuan [1 ]
Ding, Xinyu [1 ]
Shao, Jingrong [2 ]
Yang, Mengxue [2 ]
Du, Dongdong [3 ]
Hu, Jiayi [4 ]
Wei, Ya [1 ]
Shen, Qiu [1 ]
Chen, Ze [1 ]
Zuo, Shengkai [1 ,2 ]
Wan, Chunxiao [1 ]
机构
[1] Tianjin Med Univ, Dept Phys & Rehabil Med, Gen Hosp, Tianjin, Peoples R China
[2] Tianjin Med Univ, Sch Pharm, Dept Biopharmaceut, Tianjin Key Lab Technol Enabling Dev Clin Therapeu, Tianjin, Peoples R China
[3] Tianjin Med Univ, Dept Cardiovasc Surg, Gen Hosp, Tianjin, Peoples R China
[4] Tianjin Med Univ, Sch Clinial Med, Tianjin, Peoples R China
关键词
aerobic training; endoplasmic reticulum stress; myocardial infarction; P300/CBP-associated factor; ENDOTHELIAL PROGENITOR CELLS; ENDOPLASMIC-RETICULUM STRESS; ACUTE MYOCARDIAL-INFARCTION; HEART-FAILURE; SKELETAL-MUSCLE; ACETYLATION;
D O I
10.1096/fj.202400007RR
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aerobic training (AT), an effective form of cardiac rehabilitation, has been shown to be beneficial for cardiac repair and remodeling after myocardial infarction (MI). The p300/CBP-associated factor (PCAF) is one of the most important lysine acetyltransferases and is involved in various biological processes. However, the role of PCAF in AT and AT-mediated cardiac remodeling post-MI has not been determined. Here, we found that the PCAF protein level was significantly increased after MI, while AT blocked the increase in PCAF. AT markedly improved cardiac remodeling in mice after MI by reducing endoplasmic reticulum stress (ERS). In vivo, similar to AT, pharmacological inhibition of PCAF by Embelin improved cardiac recovery and attenuated ERS in MI mice. Furthermore, we observed that both IGF-1, a simulated exercise environment, and Embelin protected from H2O2-induced cardiomyocyte injury, while PCAF overexpression by viruses or the sirtuin inhibitor nicotinamide eliminated the protective effect of IGF-1 in H9C2 cells. Thus, our data indicate that maintaining low PCAF levels plays an essential role in AT-mediated cardiac protection, and PCAF inhibition represents a promising therapeutic target for attenuating cardiac remodeling after MI.
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页数:16
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