Abu Shelbayeh Othman, Arroum Tasnim, Morris Silke, Busch Karin B
Institute of Integrative Cell Biology and Physiology, University of Münster, Schlossplatz 5, 48149 Münster, Germany.
Molecular Medicine and Genetics, Wayne State University, Detroit, MI 48202, USA.
Antioxidants (Basel). 2023 May 10;12(5):1075. doi: 10.3390/antiox12051075.
Mitochondria play a major role in ROS production and defense during their life cycle. The transcriptional activator PGC-1α is a key player in the homeostasis of energy metabolism and is therefore closely linked to mitochondrial function. PGC-1α responds to environmental and intracellular conditions and is regulated by SIRT1/3, TFAM, and AMPK, which are also important regulators of mitochondrial biogenesis and function. In this review, we highlight the functions and regulatory mechanisms of PGC-1α within this framework, with a focus on its involvement in the mitochondrial lifecycle and ROS metabolism. As an example, we show the role of PGC-1α in ROS scavenging under inflammatory conditions. Interestingly, PGC-1α and the stress response factor NF-κB, which regulates the immune response, are reciprocally regulated. During inflammation, NF-κB reduces PGC-1α expression and activity. Low PGC-1α activity leads to the downregulation of antioxidant target genes resulting in oxidative stress. Additionally, low PGC-1α levels and concomitant oxidative stress promote NF-κB activity, which exacerbates the inflammatory response.
线粒体在其生命周期中的活性氧(ROS)产生和防御过程中发挥着主要作用。转录激活因子PGC-1α是能量代谢稳态的关键参与者,因此与线粒体功能密切相关。PGC-1α对环境和细胞内条件作出反应,并受SIRT1/3、线粒体转录因子A(TFAM)和腺苷酸活化蛋白激酶(AMPK)的调节,这些也是线粒体生物发生和功能的重要调节因子。在本综述中,我们着重介绍了PGC-1α在此框架内的功能和调控机制,重点关注其在线粒体生命周期和ROS代谢中的作用。例如,我们展示了PGC-1α在炎症条件下清除ROS中的作用。有趣的是,PGC-1α与调节免疫反应的应激反应因子核因子-κB(NF-κB)相互调节。在炎症过程中,NF-κB降低PGC-1α的表达和活性。低水平的PGC-1α活性导致抗氧化靶基因的下调,从而导致氧化应激。此外,低水平的PGC-1α和随之而来的氧化应激会促进NF-κB的活性,进而加剧炎症反应。