Center for Cardiovascular Medicine, First Hospital of Jilin University, Changchun, China.
Front Endocrinol (Lausanne). 2021 Nov 3;12:751020. doi: 10.3389/fendo.2021.751020. eCollection 2021.
Sestrin2 is a highly conserved protein that can be induced under a variety of stress conditions, including DNA damage, oxidative stress, endoplasmic reticulum (ER) stress, and metabolic stress. Numerous studies have shown that the AMP-activated protein kinase (AMPK)/mammalian target of rapamycin (mTOR) signaling pathway has a crucial role in the regulation of metabolism. Sestrin2 regulates metabolism a number of pathways, including activation of AMPK, inhibition of the mTOR complex 1 (mTORC1), activation of mTOR complex 2 (mTORC2), inhibition of ER stress, and promotion of autophagy. Therefore, modulation of Sestrin2 activity may provide a potential therapeutic target for the prevention of metabolic diseases such as insulin resistance, diabetes, obesity, non-alcoholic fatty liver disease, and myocardial ischemia/reperfusion injury. In this review, we examined the regulatory relationship between Sestrin2 and the AMPK/mTOR signaling pathway and the effects of Sestrin2 on energy metabolism.
Sesrtein2 是一种高度保守的蛋白质,可在多种应激条件下诱导,包括 DNA 损伤、氧化应激、内质网 (ER) 应激和代谢应激。许多研究表明,AMP 激活的蛋白激酶 (AMPK)/雷帕霉素靶蛋白 (mTOR) 信号通路在调节代谢中具有关键作用。Sesrtein2 通过多种途径调节代谢,包括激活 AMPK、抑制 mTOR 复合物 1 (mTORC1)、激活 mTOR 复合物 2 (mTORC2)、抑制 ER 应激和促进自噬。因此,调节 Sesrtein2 的活性可能为预防代谢疾病(如胰岛素抵抗、糖尿病、肥胖、非酒精性脂肪性肝病和心肌缺血/再灌注损伤)提供一个潜在的治疗靶点。在这篇综述中,我们研究了 Sesrtein2 与 AMPK/mTOR 信号通路之间的调节关系以及 Sesrtein2 对能量代谢的影响。