结扎
心肌梗塞
压力过载
收缩
信使核糖核酸
内科学
基因表达
免疫印迹
生物
医学
心脏病学
肌肉肥大
内分泌学
基因
心肌肥大
生物化学
作者
Tatsuya Kiji,Yoshiko Dohi,Shin Takasawa,Hiroshi Okamoto,Akitaka Nonomura,Shigeki Taniguchi
出处
期刊:American Journal of Physiology-heart and Circulatory Physiology
[American Physical Society]
日期:2005-03-19
卷期号:289 (1): H277-H284
被引量:30
标识
DOI:10.1152/ajpheart.01206.2004
摘要
Recently, the regenerating gene (Reg) has been documented to play an important role in various regenerating tissues, but it is unknown whether the Reg gene could be activated in the heart. The aim of this study was to reveal the transcriptional activation of Reg in the heart in response to heart stress. We first found REG-1 protein expression in human hearts obtained from autopsied patients who died of myocardial infarction. REG protein was immunohistochemically stained in a fine granular pattern in the cytoplasm of cardiomyocytes. To demonstrate the activation profiles of Reg gene expression in the heart, we quantified the levels of Reg-1 mRNA in rat hearts after coronary artery ligation using real-time RT-PCR. Transient Reg-1 mRNA activation, peaking at 12 h after coronary ligation, was observed mainly in the atria, which was sevenfold higher compared with hearts with pressure overload due to aortic constriction. In contrast, Reg receptor mRNA was expressed intensely in damaged ventricles. Furthermore, Western blot analysis showed the corresponding pattern of Reg protein secretion into the serum after loading, and circulating levels of the protein after myocardial infarction were higher than those after aortic constriction. In conclusion, our results demonstrate for the first time the presence of the Reg/Reg receptor system in damaged hearts. In view of emerging evidence of Reg for tissue regeneration in a variety of tissues/organs, it is proposed that the damaged heart may be a target for Reg action and that Reg may protect against acute heart stress.
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