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mitoAMPK in exercise benefits

mitoAMPK in exercise benefits
mitoAMPK 在运动中的益处
批准号:
10627998
负责人:
Zhen Yan
金额:
$43.5万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
未结题
起止时间:
2020-06-01 至 2025-05-31

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中文摘要
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PROJECT SUMMARY/ABSTRACT Regular exercise promotes physical performance and health, and prevent various types of diseases. These benefits are largely mediated by responses and adaptations, particularly mitochondrial remodeling, in skeletal muscle. 5' AMP-activated protein kinase (AMPK) is a bioenergetics sensor that is critical for the maintenance of metabolic homoeostasis, and AMPK signaling has been linked to mitochondrial remodeling and functional adaptations under normal and disease conditions. However, the precise mechanism of AMPK signaling in control of mitochondrial remodeling with subcellular specificity remains obscure. We discovered a physical association of a novel AMPK complex (α1, β2 and γ1 subunits) with mitochondria (referred to as mitoAMPK) in and unveiled its activation (T172 phosphorylation) under exercise and ischemic conditions. We have also obtained preliminary data to show that inhibition of mitoAMPK blocks exercise-induced mitophagy, a key step in mitochondrial quality control, in skeletal muscle. We now propose a completely novel hypothesis that mitoAMPK is preferentially activated at energetically stressed mitochondria during exercise, mediating precision mitophagy of dysfunctional or damaged mitochondria for functional and metabolic adaptations To test this hypothesis, we propose: 1) Determine if mitoAMPK is preferentially activated at energetically stressed mitochondria in skeletal muscle. 2) Elucidate the role of mitoAMPK in exercise-induced mitophagy. 3) Eetermine the functional role of mitoAMPK in exercise training-induced functional and metabolic adaptations. The proposed studies will capitalize on our novel findings of mitoAMPK that reveals completely new regulatory and functional features of this important signaling molecule in muscle biology and metabolism. The experimental design and model systems are both conceptually and technically innovative. The findings will significantly improve the mechanistic understanding of exercise-induced mitophagy and adaptations, with great potential impact on the future development of therapeutics for treatment and prevention ofchronic diseases, like type 2 diabetes.
期刊论文(9)
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科研奖励(0)
会议论文
DOI: 10.3389/fphys.2021.732308
发表时间: 2021
期刊: Frontiers in physiology
影响因子: 4
作者: [Drake JC, Wilson RJ, Cui D, Guan Y, Kundu M, Zhang M, Yan Z]
通讯作者: Yan Z
Endurance Exercise Training Mitigates Diastolic Dysfunction in Diabetic Mice Independent of Phosphorylation of Ulk1 at S555.
耐力运动训练可缓解与S555 ULK1磷酸化无关的糖尿病小鼠中的舒张功能障碍。
DOI: 10.3390/ijms25010633
发表时间: 2024-01-03
期刊: International journal of molecular sciences
影响因子: 5.6
作者: []
通讯作者:
DOI: 10.3390/cells11050872
发表时间: 2022-03-03
期刊: Cells
影响因子: 6
作者: [Guan Y, Yan Z]
通讯作者: Yan Z
DOI: 10.1093/brain/awac037
发表时间: 2022-07-29
期刊: Brain : a journal of neurology
影响因子: --
作者: []
通讯作者:
7
    Exercise-Induced Mitophagy In Hippocampal Neurons Against AD
    Synaptic and Genetic Mechanisms of Sex-Specific Effects of Stress
    Synaptic and Genetic Mechanisms of Sex-Specific Effects of Stress
    Synaptic and Genetic Mechanisms of Sex-Specific Effects of Stress
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