MicroRNAs miR-1, miR-133a, miR-133b and miR-208 Are Dysregulated in Human Myocardial Infarction

被引:258
作者
Bostjancic, Emanuela [1 ]
Zidar, Nina [1 ]
Stajer, Dusan [2 ]
Glavac, Damjan [1 ]
机构
[1] Univ Ljubljana, Dept Mol Genet, Inst Pathol, Fac Med, SI-1000 Ljubljana, Slovenia
[2] Univ Med Ctr, Ctr Intens Internal Med, Ljubljana, Slovenia
关键词
Cardiac-specific microRNA; Myocardial infarction; Fetal hearts; Cardiac gene reprogramming; Heart development; CARDIAC-HYPERTROPHY; MIRNA EXPRESSION; HUMAN HEART; REGULATORS; SAMPLES; DISEASE; FROZEN; MICE; PCR;
D O I
10.1159/000268088
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: MicroRNAs (miRNAs) are noncoding single-stranded RNA molecules that regulate gene expression in physiological functions, development and disease. In recent studies, three miRNAs have been described as muscle or cardiac specific: miR-1, miR-133, and miR-208, being involved in heart development and disease; but there are limited data on their role in human myocardial infarction (MI). We therefore analyzed their expression in human MI. Methods: Autopsy samples of infarcted heart tissue from 50 patients with MI, 8 healthy trauma victims and 9 fetuses that died in utero were included. miRNAs miR-1, miR-133a/b and miR-208 were analyzed using quantitative real-time polymerase chain reaction. Results: miR-208 was upregulated, whereas miR-1 and miR-133a were downregulated in MI compared to healthy adult and fetal hearts. All four tested miRNAs were downregulated in fetal hearts compared to healthy adult hearts. Conclusions: Our study showed the involvement of muscle- and/or cardiac-specific miRNAs miR-1, miR-133a/b and miR-208 in human MI. The most significant finding was upregulation of miR-208 and downregulation of miR-1 and miR-133a in MI compared to healthy adult hearts. Some patterns of miRNA expression were similar in MI and fetal hearts, supporting the concept of cardiac gene reprogramming in the remodeling of the heart. Copyright (C) 2009 S. Karger AG, Basel
引用
收藏
页码:163 / 169
页数:7
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