Increase of macrophage migration inhibitory factor (MIF) expression in cardiomyocytes during chronic hypoxia

被引:23
|
作者
Jian, Zhao [1 ]
Li, Jia-Bei [2 ]
Ma, Rui-Yan [1 ]
Chen, Lin [1 ]
Zhong, Qian-Jin [1 ]
Wang, Xue-Feng [1 ]
Wang, Wei [1 ]
Hong, Yi [1 ]
Xiao, Ying-Bin [1 ]
机构
[1] Third Mil Med Univ, Dept Cardiovasc Surg, Xinqiao Hosp, Chongqing 400037, Peoples R China
[2] Third Mil Med Univ, Inst Cardiol, Xinqiao Hosp, Chongqing 400037, Peoples R China
关键词
Cyanotic heart defects; Chronic hypoxia; Macrophage migration inhibitory factor (MIF); 5 '-adenosine monophosphate activated protein kinase (AMPK); Metabolic adaptation; ACTIVATED PROTEIN-KINASE; HEART; INJURY; STIMULATION; DYSFUNCTION; GLYCOLYSIS; METABOLISM; MECHANISMS; CYTOKINE; LKB1;
D O I
10.1016/j.cca.2009.04.016
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Macrophage migration inhibitory factor (MIF) might play an important role in the myocardium during chronic hypoxia because MIF protects the heart during myocardial ischemia by activating 5'-adenosine monophosphate activated protein kinase (AMPK). Methods: We investigated 35 infants with cyanotic or acyanotic cardiac defects and H9c2 embryonic rat cardiomyocytes to examine the effect of chronic hypoxia on the expression of MIF in vivo and in vitro, respectively. Results: We found out an increase of endogenous cardiac MIF expression positively correlated with degree of hypoxia. Also, AMPK activation was elevated while MIF expression was increased in cells exposed to long periods of hypoxia in vitro. There was no significant difference in the growth ratio of cells cultivated in long periods of hypoxia and normoxia. Conclusions: The expression of MIF is significantly increased in cardiomyocytes exposed to chronic hypoxia, and the activation of AMPK was increased accordingly. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:132 / 138
页数:7
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