肽
IκB激酶
NF-κB
炎症
化学
细胞生物学
NFKB1型
生物
医学
内科学
生物化学
转录因子
基因
作者
Hansen Liu,Zhenzhen Yan,Yunpeng Zhao,Xiaoyuan Ma,Honghai Zhang,Xueer Wang,Wanxin Zhuang,Yi Zheng,Bingyu Liu,Lei Zhang,Chengjiang Gao
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2021-08-23
卷期号:207 (6): 1652-1661
被引量:8
标识
DOI:10.4049/jimmunol.2100397
摘要
Abstract The IκB kinase (IKK) complex plays a vital role in regulating the NF-κB activation. Aberrant NF-κB activation is involved in various inflammatory diseases. Thus, targeting IKK activation is an ideal therapeutic strategy to cure and prevent inflammatory diseases related to NF-κB activation. In a previous study, we demonstrated that IKK-interacting protein (IKIP) inhibits the phosphorylation of IKKα/β and the activation of NF-κB through disruption of the formation of IKK complex. In this study, we identified a 15-aa peptide derived from mouse IKIP (46–60 aa of IKIP), which specifically suppressed IKK activation and NF-κB targeted gene expression via disrupting the association of IKKβ and NEMO. Importantly, administration of the peptide reduced LPS-induced acute inflammation and attenuated Zymosan-induced acute arthritis in mice. These findings suggest that this IKIP peptide may be a promising therapeutic reagent in the prevention and treatment of inflammatory diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI