Orogo Amabel M, Gustafsson Åsa B
From the Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, La Jolla.
Circ Res. 2015 Jan 30;116(3):489-503. doi: 10.1161/CIRCRESAHA.116.303791.
Autophagy is an evolutionarily conserved process by which long-lived proteins and organelles are sequestered by autophagosomes and subsequently degraded by lysosomes for recycling. Autophagy is important for maintaining cardiac homeostasis and is a survival mechanism that is upregulated during stress or starvation. Accumulating evidence suggests that dysregulated or reduced autophagy is associated with heart failure and aging. Thus, modulating autophagy represents an attractive future therapeutic target for treating cardiovascular disease. Activation of autophagy is generally considered to be cardioprotective, whereas excessive autophagy can lead to cell death and cardiac atrophy. It is important to understand how autophagy is regulated to identify ideal therapeutic targets for treating disease. Here, we discuss the key proteins in the core autophagy machinery and describe upstream regulators that respond to extracellular and intracellular signals to tightly coordinate autophagic activity. We review various genetic and pharmacological studies that demonstrate the important role of autophagy in the heart and consider the advantages and limitations of approaches that modulate autophagy.
自噬是一个进化上保守的过程,通过该过程,长寿蛋白和细胞器被自噬体隔离,随后被溶酶体降解以进行再循环。自噬对于维持心脏内环境稳定很重要,并且是一种在应激或饥饿期间上调的生存机制。越来越多的证据表明,自噬失调或减少与心力衰竭和衰老有关。因此,调节自噬是治疗心血管疾病未来一个有吸引力的治疗靶点。自噬的激活通常被认为具有心脏保护作用,而过度自噬可导致细胞死亡和心脏萎缩。了解自噬如何被调节对于确定治疗疾病的理想治疗靶点很重要。在这里,我们讨论核心自噬机制中的关键蛋白,并描述响应细胞外和细胞内信号以紧密协调自噬活性的上游调节因子。我们回顾了各种遗传和药理学研究,这些研究证明了自噬在心脏中的重要作用,并考虑了调节自噬方法的优点和局限性。