运动驱动的细胞自噬:通往系统健康的桥梁

IF 11.4 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Journal of Advanced Research Pub Date : 2025-01-03 DOI:10.1016/j.jare.2024.12.036
Xiao-Han Zhou, Ya-Xi Luo, Xiu-Qing Yao
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引用次数: 0

摘要

运动通过支持体内平衡、增强防御和帮助疾病恢复来增强健康。它激活自噬,这是一个保守的细胞过程,对维持平衡至关重要,而失调的自噬有助于疾病的进展。尽管对运动和自噬进行了广泛的独立研究,但它们之间的相互作用仍然没有得到充分的了解。本文综述了运动诱导的自噬在不同组织中的分子机制,重点探讨了关键的转导途径。它研究了不同类型的运动如何触发特定的自噬反应,支持细胞平衡和解决全身功能障碍。该综述还强调了所涉及的信号通路,以及它们在保护器官功能、降低疾病风险和促进寿命方面的作用,为运动和自噬之间的联系提供了清晰的认识。综述的关键科学概念运动诱导的自噬是由高度协调和动态的途径控制的,整合了直接和间接的机械力和生化信号,将身体活动与多器官系统的细胞和系统健康联系起来。它的激活受运动方式、强度、持续时间和个体生物学特征(包括年龄、性别和肌纤维组成)的影响。有氧运动主要参与AMPK和mTOR通路,支持线粒体质量和细胞稳态。无氧训练激活PI3K/Akt信号,调节FOXO3a和Beclin1等分子驱动肌肉自噬和修复。在病理背景下,运动诱导的自噬增强了线粒体功能、蛋白质平衡和组织再生,有利于肌肉减少症、神经变性、心肌缺血、代谢紊乱和癌症等疾病。然而,过度运动可能导致自噬过度激活,导致肌肉萎缩或病理性心脏重塑。这强调了平衡运动方案的重要性,以最大限度地提高治疗效果,同时最大限度地降低风险。未来的研究应优先确定可靠的生物标志物,优化运动方案,并将运动与药物策略结合起来,以提高治疗效果。
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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Exercise-driven cellular autophagy: A bridge to systematic wellness

Background

Exercise enhances health by supporting homeostasis, bolstering defenses, and aiding disease recovery. It activates autophagy, a conserved cellular process essential for maintaining balance, while dysregulated autophagy contributes to disease progression. Despite extensive research on exercise and autophagy independently, their interplay remains insufficiently understood.

Aim of Review

This review explores the molecular mechanisms of exercise-induced autophagy in various tissues, focusing on key transduction pathways. It examines how different types of exercise trigger specific autophagic responses, supporting cellular balance and addressing systemic dysfunctions. The review also highlights the signaling pathways involved, their roles in protecting organ function, reducing disease risk, and promoting longevity, offering a clear understanding of the link between exercise and autophagy.

Key Scientific Concepts of Review

Exercise-induced autophagy is governed by highly coordinated and dynamic pathways integrating direct and indirect mechanical forces and biochemical signals, linking physical activity to cellular and systemic health across multiple organ systems. Its activation is influenced by exercise modality, intensity, duration, and individual biological characteristics, including age, sex, and muscle fiber composition. Aerobic exercises primarily engage AMPK and mTOR pathways, supporting mitochondrial quality and cellular homeostasis. Anaerobic training activates PI3K/Akt signaling, modulating molecules like FOXO3a and Beclin1 to drive muscle autophagy and repair. In pathological contexts, exercise-induced autophagy enhances mitochondrial function, proteostasis, and tissue regeneration, benefiting conditions like sarcopenia, neurodegeneration, myocardial ischemia, metabolic disorders, and cancer. However, excessive exercise may lead to autophagic overactivation, leading to muscle atrophy or pathological cardiac remodeling. This underscores the critical need for balanced exercise regimens to maximize therapeutic efficacy while minimizing risks. Future research should prioritize identifying reliable biomarkers, optimizing exercise protocols, and integrating exercise with pharmacological strategies to enhance therapeutic outcomes.
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来源期刊
Journal of Advanced Research
Journal of Advanced Research Multidisciplinary-Multidisciplinary
CiteScore
21.60
自引率
0.90%
发文量
280
审稿时长
12 weeks
期刊介绍: Journal of Advanced Research (J. Adv. Res.) is an applied/natural sciences, peer-reviewed journal that focuses on interdisciplinary research. The journal aims to contribute to applied research and knowledge worldwide through the publication of original and high-quality research articles in the fields of Medicine, Pharmaceutical Sciences, Dentistry, Physical Therapy, Veterinary Medicine, and Basic and Biological Sciences. The following abstracting and indexing services cover the Journal of Advanced Research: PubMed/Medline, Essential Science Indicators, Web of Science, Scopus, PubMed Central, PubMed, Science Citation Index Expanded, Directory of Open Access Journals (DOAJ), and INSPEC.
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