Department of Cell and Molecular Physiology, McAllister Heart Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Exp Gerontol. 2011 Feb-Mar;46(2-3):185-8. doi: 10.1016/j.exger.2010.09.010. Epub 2010 Oct 1.
Aging is a key risk factor associated with the onset of cardiovascular disease. Notably, vascular aging and cardiovascular disease are both associated with endothelial dysfunction, or a marked decrease in production and bioavailability the vasodilator of nitric oxide (NO). As a result of decreased nitric oxide availability, aging vessels often exhibit endothelial cell senescence and increased oxidative stress. One of the most potent activators of NO production is fluid shear stress produced by blood flow. Interestingly, age-related decrease in NO production partially results from endothelial insensitivity to shear stress. While the endothelial cell response to fluid shear stress has been well characterized in recent years, the exact mechanisms of how the mechanical force of fluid shear stress is converted into intracellular biochemical signals are relatively unknown. Therefore, gaining a better knowledge of mechanosignaling events in endothelial cells may prove to be beneficial for developing potential therapies for cardiovascular diseases.
衰老是与心血管疾病发病相关的一个关键风险因素。值得注意的是,血管衰老和心血管疾病都与内皮功能障碍有关,即血管舒张因子一氧化氮(NO)的产生和生物利用度显著下降。由于一氧化氮供应减少,衰老的血管常常表现出内皮细胞衰老和氧化应激增加。促进一氧化氮产生的最有效物质之一是血流产生的流体切应力。有趣的是,与年龄相关的 NO 产生减少部分是由于内皮细胞对切应力不敏感。虽然近年来已经很好地描述了内皮细胞对流体切应力的反应,但将流体切应力的机械力转化为细胞内生化信号的确切机制尚不清楚。因此,更好地了解内皮细胞中的机械信号事件可能有助于开发心血管疾病的潜在治疗方法。