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Kwon, Hyug Moo
Immunometabolism and Cancer Lab.
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TonEBP Suppresses the HO-1 Gene by Blocking Recruitment of Nrf2 to Its Promoter

Author(s)
Yoo, Eun JinLee, Hwan HeeYe, Byeong JinLee, Jun HoLee, Chae YoungKang, Hyun JeJeong, Gyu WonPark, HyunLim, Sun WooLee-Kwon, WhaseonKwon, Hyug MooChoi, Soo Youn
Issued Date
2019-04
DOI
10.3389/fimmu.2019.00850
URI
https://scholarworks.unist.ac.kr/handle/201301/30418
Fulltext
https://www.frontiersin.org/articles/10.3389/fimmu.2019.00850/full
Citation
FRONTIERS IN IMMUNOLOGY, v.10, pp.850
Abstract
TonEBP is a key transcriptional activator in macrophages with an M1 phenotype. High expression of TonEBP is associated with many inflammatory diseases. Heme oxygenase-1 (HO-1), a stress-inducible protein, is induced by various oxidative and inflammatory signals, and its expression is regarded as an adaptive cellular response to inflammation and oxidative injury. Here, we show that TonEBP suppresses expression of HO-1 by blocking Nrf2 binding to the HO-1 promoter, thereby inducing polarization of macrophages to the M1 phenotype. Inhibition of HO-1 expression or activity significantly reduced the inhibitory responses on M1 phenotype and stimulatory effects on M2 phenotype by TonEBP knockdown. Additional experiments showed that HO-1 plays a role in the paracrine anti-inflammatory effects of TonEBP knockdown in macrophages. Identification of HO-1 as a downstream effector of TonEBP provides new possibilities for improved therapeutic approaches to inflammatory diseases.
Publisher
FRONTIERS MEDIA SA
ISSN
1664-3224
Keyword (Author)
NFAT5M1 macrophagesM2 macrophagesinflammationinnate immunity
Keyword
HEME OXYGENASE-1/CARBON MONOXIDEENHANCER-BINDING PROTEINHUMAN ENDOTHELIAL-CELLSTRANSCRIPTION FACTORALTERNATIVE ACTIVATIONOXIDATIVE STRESSM2 MACROPHAGESNUCLEAR-FACTORINDUCTIONEXPRESSION

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