α-酮戊二酸促进心肌细胞增殖和心肌梗死后的心脏再生

IF 9.4 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Yu Shi, Miao Tian, Xiaofang Zhao, Luxun Tang, Feng Wang, Hao Wu, Qiao Liao, Hongmei Ren, Wenbin Fu, Shuo Zheng, Pedro A. Jose, Liangpeng Li, Chunyu Zeng
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引用次数: 0

摘要

新生哺乳动物心脏受伤后可通过心肌细胞增殖实现再生,但到出生后第 7 天就会失去这种潜力。如何刺激成年心肌细胞重新进入细胞周期仍不清楚。在这里,我们发现心肌细胞的增殖取决于其新陈代谢状态。鉴于三羧酸循环与细胞增殖之间的联系,我们分析了小鼠心脏从出生后第 0.5 天到第 7 天的代谢物,发现α-酮戊二酸在减少的代谢物中排名最高。注射α-酮戊二酸可延长心脏发育过程中心肌细胞增殖的窗口期,并通过诱导成年心肌细胞增殖促进心肌梗死后的心脏再生。经 Ogdh-siRNA 处理的小鼠体内α-酮戊二酸水平升高,证实了这一点。从机理上讲,α-酮戊二酸会减少心肌细胞细胞周期基因启动子上的 H3K27me3 沉积。因此,α-酮戊二酸通过JMJD3依赖性去甲基化促进心肌细胞增殖,为治疗心肌梗死提供了一种潜在的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

α-Ketoglutarate promotes cardiomyocyte proliferation and heart regeneration after myocardial infarction

α-Ketoglutarate promotes cardiomyocyte proliferation and heart regeneration after myocardial infarction
The neonatal mammalian heart can regenerate following injury through cardiomyocyte proliferation but loses this potential by postnatal day 7. Stimulating adult cardiomyocytes to reenter the cell cycle remains unclear. Here we show that cardiomyocyte proliferation depends on its metabolic state. Given the connection between the tricarboxylic acid cycle and cell proliferation, we analyzed these metabolites in mouse hearts from postnatal day 0.5 to day 7 and found that α-ketoglutarate ranked highest among the decreased metabolites. Injection of α-ketoglutarate extended the window of cardiomyocyte proliferation during heart development and promoted heart regeneration after myocardial infarction by inducing adult cardiomyocyte proliferation. This was confirmed in Ogdh-siRNA-treated mice with increased α-ketoglutarate levels. Mechanistically, α-ketoglutarate decreases H3K27me3 deposition at the promoters of cell cycle genes in cardiomyocytes. Thus, α-ketoglutarate promotes cardiomyocyte proliferation through JMJD3-dependent demethylation, offering a potential approach for treating myocardial infarction. Yu Shi et al. show that the citric acid cycle metabolite α-ketoglutarate promotes cardiomyocyte proliferation during heart development and promotes heart regeneration after myocardial infarction.
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