Key result
Transient Reg-1 mRNA activation peaked at 12 hours after coronary ligation in rat atria, which was sevenfold higher compared with hearts subjected to pressure overload from aortic constriction.
Why the study?
Does acute heart stress activate the regenerating gene (Reg) in human and rat hearts?
Does acute heart stress activate the regenerating gene (Reg) in human and rat hearts?
Effect estimate: sevenfold higher
The regenerating gene (Reg) and its receptor system are activated in damaged hearts following acute stress, suggesting a potential role in cardiac tissue regeneration and protection.
Supports injury-specific Reg-1 activation in rat ischemia models; leaves open translation to human cardiac regeneration or therapy.
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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Kiji et al. (2005) studied Myocardial infarction / acute heart stress. Coronary artery ligation (myocardial infarction) vs. Aortic constriction (pressure overload) was evaluated on Reg-1 mRNA and protein expression levels (sevenfold higher). Transient Reg-1 mRNA activation peaked at 12 hours after coronary ligation in rat atria, which was sevenfold higher compared with hearts subjected to pressure overload from aortic constriction.
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