Division of Pulmonary, Critical Care Medicine, and Sleep, Department of Medicine, Baylor College of Medicine, Houston, Texas 77030, USA.
J Biol Chem. 2011 Jan 28;286(4):2559-66. doi: 10.1074/jbc.M110.149153. Epub 2010 Oct 22.
Mechanical loading of muscles by intrinsic muscle activity or passive stretch leads to an increase in the production of reactive oxygen species. The NAD-dependent protein deacetylase SIRT1 is involved in the protection against oxidative stress by enhancing FOXO-driven Sod2 transcription. In this report, we unravel a mechanism triggered by mechanical stretch of skeletal muscle cells that leads to an EGR1-dependent transcriptional activation of the Sirt1 gene. The resulting transient increase in SIRT1 expression generates an antioxidative response that contributes to reactive oxygen species scavenging.
肌肉的内在肌肉活动或被动拉伸产生的机械负荷会导致活性氧的产生增加。NAD 依赖性蛋白去乙酰化酶 SIRT1 通过增强 FOXO 驱动的 Sod2 转录参与对抗氧化应激的保护。在本报告中,我们揭示了一种由骨骼肌细胞机械拉伸引发的机制,该机制导致 EGR1 依赖性 Sirt1 基因的转录激活。由此产生的 SIRT1 表达的短暂增加会产生抗氧化反应,有助于清除活性氧。