Kubli Dieter A, Gustafsson Asa B
Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, CA 92093, USA.
Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, CA 92093, USA.
Trends Endocrinol Metab. 2014 Mar;25(3):156-64. doi: 10.1016/j.tem.2013.11.004. Epub 2013 Dec 24.
Autophagy is important in the heart for maintaining homeostasis when changes in nutrient levels occur. Autophagy is involved in the turnover of cellular components, and is rapidly upregulated during stress. Studies have found that autophagy is reduced in metabolic disorders including obesity and diabetes. This leads to accumulation of protein aggregates and dysfunctional organelles, which contributes to the pathogenesis of cardiovascular disease. Autophagy is primarily regulated by two components: the mechanistic target of rapamycin (mTOR) and AMP-activated protein kinase (AMPK). Although mTOR integrates information about growth factors and nutrients and is a negative regulator of autophagy, AMPK is an energy sensor and activates autophagy when energy levels are low. These pathways therefore present targets for the development of autophagy-modulating therapies.
当营养水平发生变化时,自噬对于心脏维持内环境稳定至关重要。自噬参与细胞成分的更新,并在应激期间迅速上调。研究发现,在包括肥胖和糖尿病在内的代谢紊乱中自噬减少。这会导致蛋白质聚集体和功能失调的细胞器积累,进而促进心血管疾病的发病机制。自噬主要由两个成分调节:雷帕霉素机制性靶标(mTOR)和AMP激活的蛋白激酶(AMPK)。虽然mTOR整合有关生长因子和营养物质的信息,是自噬的负调节因子,但AMPK是一种能量传感器,在能量水平低时激活自噬。因此,这些途径为自噬调节疗法的开发提供了靶点。