Variation of NDRG2 and c-Myc expression in rat heart during the acute stage of ischemia/reperfusion injury

被引:29
|
作者
Sun, Zhongchan [1 ]
Shen, Lan [2 ]
Sun, Xiang [3 ]
Tong, Guang [4 ]
Sun, Dongdong [1 ]
Han, Tenglong [2 ]
Yang, Guodong [2 ]
Zhang, Jian [2 ]
Cao, Feng [1 ]
Yao, Libo [2 ]
Wang, Haichang [1 ]
机构
[1] Fourth Mil Med Univ, Xijing Hosp, Dept Cardiovasc Med, 15 Changle Western Rd, Xian 710032, Peoples R China
[2] Fourth Mil Med Univ, State Key Lab Canc Biol, Dept Biochem & Mol Biol, Xian 710032, Peoples R China
[3] Fourth Mil Med Univ, Sch Stomatol, Dept Prosthodont, Xian 710032, Peoples R China
[4] Fourth Mil Med Univ, Xijing Hosp, Dept Cardiovasc Surg, Xian 710032, Peoples R China
基金
中国国家自然科学基金;
关键词
NDRG2; Ischemia/reperfusion; c-Myc; Apoptosis; Myocardium; DOWNSTREAM-REGULATED GENE-2; REPERFUSION INJURY; HYPOXIA; APOPTOSIS; INSULIN; BRAIN; HIF-1; MICE;
D O I
10.1007/s00418-010-0776-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
N-Myc downstream regulated gene 2 (NDRG2), a Myc-repressed gene, is highly expressed in heart tissue. NDRG2 increases in response to hypoxia-induced stress and is involved in hypoxia-induced radioresistance. However, little is known about the expression changes and possible roles of NDRG2 in the heart under hypoxia condition. Here, the authors show that NDRG2, mainly localized in cardiomyocyte cytoplasm, was significantly reduced in myocardial tissue after acute ischemia/reperfusion (I/R) injury. Meanwhile, c-Myc was up-regulated following acute I/R injury, and the expression of c-Myc was significantly inversely correlated with that of NDRG2. In addition, overexpression of c-Myc in primary cultured cardiomyocyte repressed NDRG2 expression. Furthermore, the increase of cardiomyocyte apoptosis was correlated with the decrease of NDRG2 protein during the acute phase of reperfusion. These data suggested for the first time that I/R injury-induced upregulation of pro-apoptotic c-Myc expression may contribute to the down-regulation of anti-apoptotic NDRG2. This stress response might be involved in the novel mechanism of myocardial apoptosis induced by I/R injury in rat.
引用
收藏
页码:27 / 35
页数:9
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