Calcium-mediated regulation of mitophagy: implications in neurodegenerative diseases.

npj Metabolic Health and Disease Pub Date : 2025-01-01 Epub Date: 2025-02-03 DOI:10.1038/s44324-025-00049-2
Fivos Borbolis, Christina Ploumi, Konstantinos Palikaras
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引用次数: 0

Abstract

Calcium signaling plays a pivotal role in diverse cellular processes through precise spatiotemporal regulation and interaction with effector proteins across distinct subcellular compartments. Mitochondria, in particular, act as central hubs for calcium buffering, orchestrating energy production, redox balance and apoptotic signaling, among others. While controlled mitochondrial calcium uptake supports ATP synthesis and metabolic regulation, excessive accumulation can trigger oxidative stress, mitochondrial membrane permeabilization, and cell death. Emerging findings underscore the intricate interplay between calcium homeostasis and mitophagy, a selective type of autophagy for mitochondria elimination. Although the literature is still emerging, this review delves into the bidirectional relationship between calcium signaling and mitophagy pathways, providing compelling mechanistic insights. Furthermore, we discuss how disruptions in calcium homeostasis impair mitophagy, contributing to mitochondrial dysfunction and the pathogenesis of common neurodegenerative diseases.

钙介导的线粒体自噬调控:在神经退行性疾病中的意义。
钙信号通过精确的时空调节和与不同亚细胞区室的效应蛋白的相互作用,在多种细胞过程中起着关键作用。尤其是线粒体,在钙缓冲、协调能量产生、氧化还原平衡和凋亡信号等方面起着中心枢纽的作用。虽然受控制的线粒体钙摄取支持ATP合成和代谢调节,但过度积累可引发氧化应激、线粒体膜渗透和细胞死亡。新发现强调了钙稳态和线粒体自噬之间复杂的相互作用,线粒体自噬是线粒体消除的一种选择性自噬。尽管相关文献仍在不断涌现,但本综述深入探讨了钙信号和有丝分裂途径之间的双向关系,提供了令人信服的机制见解。此外,我们讨论了钙稳态的破坏如何损害线粒体自噬,导致线粒体功能障碍和常见神经退行性疾病的发病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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