mitoAMPK in exercise benefits
mitoAMPK in exercise benefits
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
关键词:
5&apos-AMP-activated protein kinaseAdenine NucleotidesAdultAutophagocytosisBioenergeticsBiological ModelsBiologyCRISPR/Cas technologyChronic DiseaseColorComplexCultured CellsDataDeteriorationDevelopmentDiabetes MellitusDiseaseDynaminElectric StimulationEnsureEnzymesExerciseExperimental DesignsExperimental ModelsFluorescenceFluorescence Resonance Energy TransferFoundationsFutureGene TransferHealth BenefitHealth PromotionHeartHoloenzymesHumanImageInsulin ResistanceInterventionIschemiaKidneyKnockout MiceLaboratoriesLinkMaintenanceMediatingMembrane PotentialsMetabolicMetabolismMitochondriaMotorMusMuscleMuscle CellsMuscle ContractionNerveNon-Insulin-Dependent Diabetes MellitusNutrientOuter Mitochondrial MembraneOxidative PhosphorylationOxidative StressPhosphorylationPhosphotransferasesPhysical PerformancePower PlantsPreventionProcessProductionProteinsQuality ControlReactive Oxygen SpeciesRegulationReporterRoleRunningSignal TransductionSignaling MoleculeSkeletal MuscleSpecificityStressTechnologyTestingTissuesVisualizationeffective interventionendurance exerciseexercise capacityexercise trainingfightingfrailtyfunctional adaptationgain of functionimprovedin vivoinhibitorinnovationinsulin sensitivityloss of functionnovelpharmacologicphysical conditioningpreventresponsesensorskeletaltherapeutic developmenttherapeutically effectivetreadmilltwo-photon
中文摘要
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英文摘要
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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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:
DOI:
10.1146/annurev-physiol-060721-095517
发表时间:
2022-02-10
期刊:
Annual review of physiology
影响因子:
18.2
作者:
[Spaulding HR, Yan Z]
通讯作者:
Yan Z
共 7 条
Exercise-Induced Mitophagy In Hippocampal Neurons Against AD
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批准号:10765466
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项目类别:
-
资助金额:$55.52万
-
财政年份:2022
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负责人:Zhen Yan
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依托单位:
Synaptic and Genetic Mechanisms of Sex-Specific Effects of Stress
-
批准号:10380087
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项目类别:
-
资助金额:$52.99万
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财政年份:2021
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负责人:Zhen Yan
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依托单位:
Synaptic and Genetic Mechanisms of Sex-Specific Effects of Stress
-
批准号:10551274
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项目类别:
-
资助金额:$50.21万
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财政年份:2021
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负责人:Zhen Yan
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依托单位:
Synaptic and Genetic Mechanisms of Sex-Specific Effects of Stress
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批准号:10225076
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项目类别:
-
资助金额:$55.78万
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财政年份:2021
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负责人:Zhen Yan
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依托单位:
mitoAMPK in exercise benefits
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批准号:10172852
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项目类别:
-
资助金额:$42.59万
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财政年份:2020
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负责人:Zhen Yan
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依托单位:
Machine learning-based multi-omics modeling and CRISPR/Cas9-mediated gene editing in elucidating molecular transducer of physical activity
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批准号:10771467
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项目类别:
-
资助金额:$39.6万
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财政年份:2020
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负责人:Zhen Yan
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依托单位:
Machine learning-based multi-omics modeling and CRISPR/Cas9-mediated gene editing in elucidating molecular transducer of physical activity
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批准号:10413230
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项目类别:
-
资助金额:$8.46万
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财政年份:2020
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负责人:Zhen Yan
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依托单位:
mitoAMPK in exercise benefits
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批准号:10408037
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项目类别:
-
资助金额:$0.0万
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财政年份:2020
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负责人:Zhen Yan
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依托单位:
mitoAMPK in exercise benefits
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批准号:10765945
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项目类别:
-
资助金额:$43.06万
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财政年份:2020
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负责人:Zhen Yan
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依托单位:
Machine learning-based multi-omics modeling and CRISPR/Cas9-mediated gene editing in elucidating molecular transducer of physical activity
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批准号:10264175
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项目类别:
-
资助金额:$52.18万
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财政年份:2020
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负责人:Zhen Yan
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依托单位:
Targeting Histone K4 Methylation for Treatment of Alzheimer's Disease and Related Dementia
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批准号:10599193
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项目类别:
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资助金额:$50.64万
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财政年份:2019
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负责人:Zhen Yan
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依托单位:
Targeting Histone K4 Methylation for Treatment of Alzheimer's Disease and Related Dementia
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批准号:10385819
-
项目类别:
-
资助金额:$50.64万
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财政年份:2019
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负责人:Zhen Yan
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依托单位:
Targeting Histone K4 Methylation for Treatment of Alzheimer's Disease and Related Dementia
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批准号:9812686
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项目类别:
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资助金额:$50.64万
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财政年份:2019
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负责人:Zhen Yan
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依托单位:
A Novel Epigenetic Mechanism for Alzheimer's Disease
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批准号:9323647
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项目类别:
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资助金额:$39.88万
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财政年份:2017
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负责人:Zhen Yan
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依托单位:
A Novel Epigenetic Mechanism for Alzheimer's Disease
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批准号:9890990
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项目类别:
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资助金额:$39.88万
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财政年份:2017
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负责人:Zhen Yan
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依托单位:
A Novel Epigenetic Mechanism for Alzheimer's Disease
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批准号:10361607
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项目类别:
-
资助金额:$6.27万
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财政年份:2017
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负责人:Zhen Yan
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依托单位:
Muscle-mediated protection against MODS
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批准号:9206172
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项目类别:
-
资助金额:$30.02万
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财政年份:2015
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负责人:Zhen Yan
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依托单位:
Muscle-mediated protection against MODS
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批准号:9041638
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项目类别:
-
资助金额:$30.02万
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财政年份:2015
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负责人:Zhen Yan
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依托单位:
Request for Nikon N-SIM/N-STORM Super Resolution Microscope
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批准号:8947858
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项目类别:
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资助金额:$0.0万
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财政年份:2015
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负责人:Zhen Yan
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Synaptic Functions of Disrupted-in-Schizophrenia-1 (DISC1)
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批准号:8703804
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项目类别:
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资助金额:$23.79万
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负责人:Zhen Yan
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依托单位:
海外基金