| Literature DB >> 28467930 |
Sung-Jun Park1, Oksana Gavrilova2, Alexandra L Brown1, Jamie E Soto3, Shannon Bremner4, Jeonghan Kim1, Xihui Xu1, Shutong Yang1, Jee-Hyun Um1, Lauren G Koch5, Steven L Britton6, Richard L Lieber4, Andrew Philp7, Keith Baar7, Steven G Kohama8, E Dale Abel3, Myung K Kim1, Jay H Chung9.
Abstract
Hallmarks of aging that negatively impact health include weight gain and reduced physical fitness, which can increase insulin resistance and risk for many diseases, including type 2 diabetes. The underlying mechanism(s) for these phenomena is poorly understood. Here we report that aging increases DNA breaks and activates DNA-dependent protein kinase (DNA-PK) in skeletal muscle, which suppresses mitochondrial function, energy metabolism, and physical fitness. DNA-PK phosphorylates threonines 5 and 7 of HSP90α, decreasing its chaperone function for clients such as AMP-activated protein kinase (AMPK), which is critical for mitochondrial biogenesis and energy metabolism. Decreasing DNA-PK activity increases AMPK activity and prevents weight gain, decline of mitochondrial function, and decline of physical fitness in middle-aged mice and protects against type 2 diabetes. In conclusion, DNA-PK is one of the drivers of the metabolic and fitness decline during aging, and therefore DNA-PK inhibitors may have therapeutic potential in obesity and low exercise capacity. Published by Elsevier Inc.Entities:
Keywords: AMPK; DNA-PK; HSP90α; aging; calorie restriction; exercise; insulin sensitivity; mitochondria; obesity; skeletal muscle; type 2 diabetes
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Year: 2017 PMID: 28467930 PMCID: PMC5485859 DOI: 10.1016/j.cmet.2017.04.008
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287