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自噬与运动:当前见解及未来研究方向

Autophagy and Exercise: Current Insights and Future Research Directions.

作者信息

Botella Javier, Shaw Christopher S, Bishop David J

机构信息

Metabolic Research Unit, School of Medicine and Institute for Mental and Physical Health and Clinical Translation (IMPACT), Deakin University, Waurn Ponds, Victoria, Australia.

Institute for Physical Activity and Nutrition (IPAN), School of Exercise and Nutrition Sciences, Deakin University, Geelong, 3216, VIC, Australia.

出版信息

Int J Sports Med. 2024 Mar;45(3):171-182. doi: 10.1055/a-2153-9258. Epub 2023 Aug 15.

Abstract

Autophagy is a cellular process by which proteins and organelles are degraded inside the lysosome. Exercise is known to influence the regulation of autophagy in skeletal muscle. However, as gold standard techniques to assess autophagy flux are restricted to animal research, important gaps remain in our understanding of how exercise influences autophagy activity in humans. Using available datasets, we show how the gene expression profile of autophagy receptors and ATG8 family members differ between human and mouse skeletal muscle, providing a potential explanation for their differing exercise-induced autophagy responses. Furthermore, we provide a comprehensive view of autophagy regulation following exercise in humans by summarizing human transcriptomic and phosphoproteomic datasets that provide novel targets of potential relevance. These newly identified phosphorylation sites may provide an explanation as to why both endurance and resistance exercise lead to an exercise-induced reduction in LC3B-II, while possibly divergently regulating autophagy receptors, and, potentially, autophagy flux. We also provide recommendations to use autophagy flux assays to better understand the influence of exercise, and other stimuli, on autophagy regulation in humans. This review provides a critical overview of the field and directs researchers towards novel research areas that will improve our understanding of autophagy regulation following exercise in humans.

摘要

自噬是一种细胞过程,通过该过程蛋白质和细胞器在溶酶体内被降解。已知运动可影响骨骼肌中自噬的调节。然而,由于评估自噬通量的金标准技术仅限于动物研究,我们对运动如何影响人类自噬活性的理解仍存在重大差距。利用现有数据集,我们展示了人类和小鼠骨骼肌中自噬受体和ATG8家族成员的基因表达谱如何不同,为它们不同的运动诱导自噬反应提供了潜在解释。此外,我们通过总结提供潜在相关新靶点的人类转录组学和磷酸蛋白质组学数据集,全面阐述了人类运动后自噬的调节。这些新发现的磷酸化位点可能解释了为什么耐力运动和抗阻运动都会导致运动诱导的LC3B-II减少,同时可能以不同方式调节自噬受体以及潜在的自噬通量。我们还提供了使用自噬通量测定法的建议,以更好地理解运动和其他刺激对人类自噬调节的影响。本综述对该领域进行了批判性概述,并引导研究人员关注新的研究领域,这些领域将增进我们对人类运动后自噬调节的理解。

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