Is Nuclear Factor Erythroid 2-Related Factor 2 a Target for the Intervention of Cytokine Storms?

被引:10
|
作者
Liu, Zihang [1 ]
Deng, Panpan [1 ]
Liu, Shengnan [2 ]
Bian, Yiying [2 ]
Xu, Yuanyuan [3 ]
Zhang, Qiang [4 ]
Wang, Huihui [3 ]
Pi, Jingbo [2 ]
机构
[1] China Med Univ, Dept Clin Med 1, Shenyang 110122, Peoples R China
[2] China Med Univ, Sch Publ Hlth, Program Environm Toxicol, Shenyang 110122, Peoples R China
[3] China Med Univ, Sch Publ Hlth, Grp Chron Dis & Environm Genom, Shenyang 110122, Peoples R China
[4] Emory Univ, Rollins Sch Publ Hlth, Dept Environm Hlth 4Gangarosa, Atlanta, GA 30322 USA
基金
中国国家自然科学基金;
关键词
NRF2; cytokine storm; cytokine; oxidative stress; inflammation; NF-KAPPA-B; ACUTE LUNG INJURY; INDUCED INFLAMMATORY RESPONSE; INFLUENZA-VIRUS INFECTION; OXIDATIVE STRESS; PPAR-GAMMA; ANTIOXIDANT RESPONSE; SIGNALING PATHWAYS; HEME OXYGENASE-1; KIDNEY INJURY;
D O I
10.3390/antiox12010172
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
The term "cytokine storm" describes an acute pathophysiologic state of the immune system characterized by a burst of cytokine release, systemic inflammatory response, and multiple organ failure, which are crucial determinants of many disease outcomes. In light of the complexity of cytokine storms, specific strategies are needed to prevent and alleviate their occurrence and deterioration. Nuclear factor erythroid 2-related factor 2 (NRF2) is a CNC-basic region-leucine zipper protein that serves as a master transcription factor in maintaining cellular redox homeostasis by orchestrating the expression of many antioxidant and phase II detoxification enzymes. Given that inflammatory response is intertwined with oxidative stress, it is reasonable to assume that NRF2 activation limits inflammation and thus cytokine storms. As NRF2 can mitigate inflammation at many levels, it has emerged as a potential target to prevent and treat cytokine storms. In this review, we summarized the cytokine storms caused by different etiologies and the rationale of interventions, focusing mainly on NRF2 as a potential therapeutic target.
引用
收藏
页数:21
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