PGC-1a Is a Master Regulator of Mitochondrial Lifecycle and ROS Stress Response

被引:204
作者
Abu Shelbayeh, Othman [1 ]
Arroum, Tasnim [1 ,2 ]
Morris, Silke [1 ]
Busch, Karin B. [1 ]
机构
[1] Univ Munster, Inst Integrat Cell Biol & Physiol, Schlosspl 5, D-48149 Munster, Germany
[2] Wayne State Univ, Mol Med & Genet, Detroit, MI 48202 USA
关键词
PGC-1; alpha; ROS defense; mitonuclear communication; mitochondrial life cycle; PROLIFERATOR-ACTIVATED-RECEPTOR; GAMMA COACTIVATOR 1-ALPHA; NUCLEAR RESPIRATORY FACTORS; SKELETAL-MUSCLE; TRANSCRIPTION FACTOR; OXIDATIVE STRESS; PGC-1-ALPHA ISOFORM; MESSENGER-RNA; INDUCIBLE COACTIVATOR; METABOLIC REGULATOR;
D O I
10.3390/antiox12051075
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondria play a major role in ROS production and defense during their life cycle. The transcriptional activator PGC-1a is a key player in the homeostasis of energy metabolism and is therefore closely linked to mitochondrial function. PGC-1a 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-1a 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-1a in ROS scavenging under inflammatory conditions. Interestingly, PGC-1a and the stress response factor NF-?B, which regulates the immune response, are reciprocally regulated. During inflammation, NF-?B reduces PGC-1a expression and activity. Low PGC-1a activity leads to the downregulation of antioxidant target genes resulting in oxidative stress. Additionally, low PGC-1a levels and concomitant oxidative stress promote NF-?B activity, which exacerbates the inflammatory response.
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页数:24
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