Medical Science Research Institute, Soonchunhyang University Seoul Hospital, Seoul 04401, Korea.
Department of Biochemistry, College of Medicine, Soonchunhyang University, Cheonan 31151, Korea.
Cells. 2021 Jul 3;10(7):1682. doi: 10.3390/cells10071682.
Dysregulation in mitophagy, in addition to contributing to imbalance in the mitochondrial dynamic, has been implicated in the development of renal fibrosis and progression of chronic kidney disease (CKD). However, the current understanding of the precise mechanisms behind the pathogenic loss of mitophagy remains unclear for developing cures for CKD. We found that miR-4516 is downregulated and its target SIAH3, an E3 ubiquitin protein ligase that reduces PINK1 accumulation to damaged mitochondria, is upregulated in the renal cortex of CKD mice. Here, we demonstrated that melatonin injection induces miR-4516 expression and suppresses SIAH3, and promotes PINK1/Parkin-mediated mitophagy. Furthermore, we demonstrated that melatonin injection attenuates the pathological features of CKD by improving mitochondrial homeostasis. Our data supports that mitochondrial autophagy regulation by activating miR-4516/SIAH3/PINK1 mitophagy signaling axis can be a viable new strategy for treating CKD.
线粒体自噬失调除了导致线粒体动态失衡外,还与肾纤维化的发展和慢性肾脏病 (CKD) 的进展有关。然而,目前对于导致线粒体自噬病理性丧失的精确机制的理解仍不清楚,无法开发出治疗 CKD 的方法。我们发现,miR-4516 在 CKD 小鼠的肾皮质中下调,其靶标 SIAH3 是一种 E3 泛素蛋白连接酶,可减少 PINK1 积累到受损的线粒体。在这里,我们证明了褪黑素注射可诱导 miR-4516 的表达并抑制 SIAH3,促进 PINK1/Parkin 介导的线粒体自噬。此外,我们证明了褪黑素注射通过改善线粒体动态平衡来减轻 CKD 的病理特征。我们的数据支持通过激活 miR-4516/SIAH3/PINK1 线粒体自噬信号轴来调节线粒体自噬,这可能是治疗 CKD 的一种可行的新策略。