细胞凋亡
标记法
心肌梗塞
再灌注损伤
自噬
心功能曲线
医学
分子生物学
缺血
内科学
男科
药理学
化学
内分泌学
生物
生物化学
心力衰竭
作者
Hee-Jung Song,Yan Cao,Xiaoxiang Tian,Nan Zhu,Yang Li,Dan Liú,Yanxia Liu,Meili Liu,Chengfei Peng,Quanyu Zhang,Erhe Gao,Yaling Han
标识
DOI:10.1016/j.bbadis.2016.11.015
摘要
Human cellular repressor of E1A-stimulated genes (CREG) is a secreted glycoprotein that regulates tissue and cell homeostasis and has been shown to antagonize heart fibrosis, which indicates a potential protective effect of CREG against cardiomyocyte chronic damage. However, little is known about the role of CREG in myocardial tissue acute injury, in this study, we aimed to investigate the role of CREG in myocardial ischemia/reperfusion (MI/R) injury and clarify the mechanism of action. Wild-type Creg (Creg+/+), heterozygous Creg (Creg+/−) mice and mice pretreated with infusion of recombinant 0.3 mg/kg·d CREG protein (reCreg+/+) were subjected to 30 min of left ascending coronary ischemia and 24 h of reperfusion. Evan's Blue-triphenyl- tetrazolium chloride (TTC) solution and echocardiography analysis were used to evaluate the effects of CREG on MI/R mice. The underlying mechanisms were further determined by cultured myocardial cells in vitro. Our findings revealed that the level of CREG protein in mouse hearts was significantly decreased after mice were subjected to MI/R. Moreover, Creg+/− mice had larger infarction size 2 h after reperfusion and worse cardiac function 28 days after MI/R injury compared to that in Creg+/+ mice. However, reCreg+/+ mice could maintain CREG at a high level even after MI/R injury, and mitigated infarction size and improved cardiac function significantly. In Creg+/− mice, myocardial autophagy was dysfunctional characterized by accumulation of LC3A and p62, while apoptotic cell number increase was detected by cleaved caspase-3 blotting and TUNEL staining. Conversely, decreased apoptosis and activated autophagy were detected in reCreg+/+ mice. Furthermore, chloroquine, a kind of autophagy blocker, was used to demonstrate recombinant CREG protected cardiomyocytes against apoptosis mediated by activating autophagy both in vivo and in vitro. Finally, we found CREG was involved into lysosomal protein transfer and improve cellular autophagy. CREG protects heart against MI/R injury-induced cardiomyocytes apoptosis by activating lysosomal autophagy. This article is part of a Special Issue entitled: Genetic and epigenetic control of heart failure - edited by Jun Ren and Megan Yingmei Zhang.
科研通智能强力驱动
Strongly Powered by AbleSci AI