Mitophagy in health and disease. Molecular mechanisms, regulatory pathways, and therapeutic implications

IF 6.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mark S. D’Arcy
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Abstract

Mitophagy, a specialised form of autophagy, selectively targeting damaged or dysfunctional mitochondria, and is crucial for maintaining cellular homeostasis and mitochondrial quality control. Dysregulation of mitophagy contributes to various pathological conditions, including cancer, neurodegenerative and cardiovascular diseases. This review presents a comprehensive analysis of the molecular mechanisms, regulatory pathways, and interplay with other cellular processes governing mitophagy, emphasizing its importance in physiological and pathological contexts. We explore the PINK1/Parkin-mediated and receptor-mediated mitophagy pathways, encompassing BNIP3/NIX, FUNDC1, and Bcl2-L-13. Additionally, we discuss post-translational modifications and cellular signalling pathways modulating mitophagy, as well as the connection between mitophagy and ageing, highlighting the decline in mitophagy efficiency and its impact on age-related pathologies. The review also investigates mitophagy's role in human diseases such as cancer, myocardial ischemia–reperfusion injury, Parkinson's, and Alzheimer's disease. We assess the potential of mitophagy-targeting therapeutic strategies, focusing on the development of dietary therapies, small molecules, drugs, and gene therapy approaches that modulate mitophagy levels and efficiency for treating these diseases and dysfunctions commonly observed in ageing individuals. In summary, this review offers an extensive overview of the molecular mechanisms and regulatory networks involved in mitophagy, its association with autophagy, and implications in human health and disease. By examining the potential of mitophagy-modulating therapies in disease and non-disease settings, we aim to inspire further research to develop innovative treatment strategies for various pathological conditions linked to mitochondrial dysfunction and to ageing.

Abstract Image

健康和疾病中的有丝分裂。分子机制、调节途径和治疗意义。
有丝分裂是自噬的一种特殊形式,它选择性地针对受损或功能障碍的线粒体,对维持细胞平衡和线粒体质量控制至关重要。有丝分裂失调会导致各种病理状况,包括癌症、神经退行性疾病和心血管疾病。本综述全面分析了控制有丝分裂的分子机制、调控途径以及与其他细胞过程的相互作用,强调了有丝分裂在生理和病理环境中的重要性。我们探讨了 PINK1/Parkin 介导和受体介导的有丝分裂途径,包括 BNIP3/NIX、FUNDC1 和 Bcl2-L-13。此外,我们还讨论了翻译后修饰和调控有丝分裂的细胞信号通路,以及有丝分裂与衰老之间的联系,强调了有丝分裂效率的下降及其对衰老相关病症的影响。这篇综述还探讨了有丝分裂在癌症、心肌缺血再灌注损伤、帕金森病和阿尔茨海默病等人类疾病中的作用。我们评估了以有丝分裂为靶点的治疗策略的潜力,重点是开发可调节有丝分裂水平和效率的饮食疗法、小分子、药物和基因治疗方法,以治疗这些疾病和衰老人群中常见的功能障碍。总之,本综述广泛概述了有丝分裂所涉及的分子机制和调控网络、有丝分裂与自噬的关联以及对人类健康和疾病的影响。通过研究线粒体吞噬调节疗法在疾病和非疾病环境中的潜力,我们旨在激发进一步的研究,为线粒体功能障碍和老龄化相关的各种病理状况开发创新的治疗策略。
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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来源期刊
Apoptosis
Apoptosis 生物-生化与分子生物学
CiteScore
9.10
自引率
4.20%
发文量
85
审稿时长
1 months
期刊介绍: Apoptosis, a monthly international peer-reviewed journal, focuses on the rapid publication of innovative investigations into programmed cell death. The journal aims to stimulate research on the mechanisms and role of apoptosis in various human diseases, such as cancer, autoimmune disease, viral infection, AIDS, cardiovascular disease, neurodegenerative disorders, osteoporosis, and aging. The Editor-In-Chief acknowledges the importance of advancing clinical therapies for apoptosis-related diseases. Apoptosis considers Original Articles, Reviews, Short Communications, Letters to the Editor, and Book Reviews for publication.
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