Teuvincenone F Suppresses LPS-Induced Inflammation and NLRP3 Inflammasome Activation by Attenuating NEMO Ubiquitination
文献类型：期刊论文
| 作者 | Zhao, Xibao1,2; Pu, Debing3,4 ; Zhao, Zizhao2; Zhu, Huihui2; Li, Hongrui1,2; Shen, Yaping2; Zhang, Xingjie3; Zhang, Ruihan3; Shen, Jianzhong5; Xiao, Weilie3,4
|
| 刊名 | FRONTIERS IN PHARMACOLOGY
 |
| 出版日期 | 2017-08-23 |
| 卷号 | 8页码:565 |
| 关键词 | Teuvincenone f Inflammation Nlrp3 Inflammasome Ubiquitination Nemo |
| ISSN号 | 1663-9812 |
| DOI | 10.3389/fphar.2017.00565 |
| 英文摘要 | Inflammation causes many diseases that are serious threats to human health. However, the molecular mechanisms underlying regulation of inflammation and inflammasome activation are not fully understood which has delayed the discovery of new anti-inflammatory drugs of urgent clinic need. Here, we found that the natural compound Teuvincenone F, which was isolated and purified from the stems and leaves of Premna szemaoensis, could significantly inhibit lipopolysaccharide (LPS)-induced pro-inflammatory cytokines production and NLRP3 inflammasome activation. Our results showed that Teuvincenone F attenuated K63-linked ubiquitination of NF-kappa B-essential modulator (NEMO, also known as IKK gamma) to suppress LPS-induced phosphorylation of NF-kappa B, and inhibited mRNA expression of IL-1 beta, IL-6, TNF-alpha, and NLRP3. In addition, we found that decreased NLRP3 expression by Teuvincenone F suppressed NLRP3 inflammasome activation and IL-1 beta/IL-18 maturation. In vivo, we revealed that Teuvincenone F treatment relieved LPS-induced inflammation. In conclusion, Teuvincenone F is a highly effective natural compound to suppress LPS-induced inflammation by attenuating K63-linked ubiquitination of NEMO, highlighting that Teuvincenone F may be a potential new anti-inflammatory drug for the treatment of inflammatory and NLRP3 inflammasome-driven diseases. |
| 学科主题 | Pharmacology & Pharmacy |
| 语种 | 英语 |
| WOS记录号 | WOS:000408517500001 |
| 源URL | [http://ir.kib.ac.cn/handle/151853/54914]  |
| 专题 | 昆明植物研究所_植物化学与西部植物资源持续利用国家重点实验室 |
| 作者单位 | 1.Shenzhen Univ, Dept Immunol, Sch Med, Shenzhen, Peoples R China 2.Zhejiang Univ, Inst Immunol, Dept Basic Med, Sch Med, Hangzhou, Zhejiang, Peoples R China 3.Yunnan Univ, Key Lab Med Chem Nat Resource, Minist Educ, Sch Chem Sci & Technol, Kunming, Yunnan, Peoples R China 4.Chinese Acad Sci, State Key Lab Phytochem & Plant Resources West Ch, Kunming Inst Bot, Kunming, Yunnan, Peoples R China 5.Auburn Univ, Dept Drug Discovery & Dev, Harrison Sch Pharm, Auburn, AL 36849 USA |
| 推荐引用方式 GB/T 7714 | Zhao, Xibao,Pu, Debing,Zhao, Zizhao,et al. Teuvincenone F Suppresses LPS-Induced Inflammation and NLRP3 Inflammasome Activation by Attenuating NEMO Ubiquitination[J]. FRONTIERS IN PHARMACOLOGY,2017,8:565. |
| APA | Zhao, Xibao.,Pu, Debing.,Zhao, Zizhao.,Zhu, Huihui.,Li, Hongrui.,...&Chen, Weilin.(2017).Teuvincenone F Suppresses LPS-Induced Inflammation and NLRP3 Inflammasome Activation by Attenuating NEMO Ubiquitination.FRONTIERS IN PHARMACOLOGY,8,565. |
| MLA | Zhao, Xibao,et al."Teuvincenone F Suppresses LPS-Induced Inflammation and NLRP3 Inflammasome Activation by Attenuating NEMO Ubiquitination".FRONTIERS IN PHARMACOLOGY 8(2017):565. |
入库方式： OAI收割
来源：昆明植物研究所
浏览0
下载0
收藏0
其他版本
除非特别说明，本系统中所有内容都受版权保护，并保留所有权利。