miR-497a-5p attenuates lipopolysaccharide-induced inflammatory injury by targeting IRAK2

被引:28
|
作者
Guo, Shuai [1 ]
Chen, Yu [1 ]
Liu, Junfeng [1 ]
Yang, Jing [1 ]
Yang, Chao [1 ]
Zhang, Tao [1 ]
Jiang, Kangfeng [1 ]
Wu, Zhimin [1 ]
Shaukat, Aftab [1 ]
Deng, Ganzhen [1 ]
机构
[1] Huazhong Agr Univ, Coll Vet Med, Dept Clin Vet Med, Wuhan 430070, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
acute lung injury; inflammation; IRAK2; LPS; miR-497; NF-KAPPA-B; ACUTE LUNG INJURY; ACTIVATION; MICRORNAS; CANCER; TRAF6;
D O I
10.1002/jcp.28850
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Acute lung injury (ALI) is a severe acute inflammatory reaction of the lungs caused by a variety of factors, which can lead to a high mortality rate. MicroRNAs are a novel therapeutic molecule that play a vital role in many diseases. However, its mechanism of action in lipopolysaccharide (LPS)-induced mouse ALI is not clear. The study aimed to investigate the mechanism of action of miR-497 in LPS-induced ALI. As a result, it was found that the expression of miR-497 in the inflammatory reaction showed a decrease in time and dose trends. Importantly, miR-497 reduced LPS-induced expression levels of related inflammatory factors. In addition, we also demonstrated that IRAK2 is a direct target molecule of miR-497. Interestingly, we further found that miR-497 inhibits the expression of IRAK2 by targeting IRAK2-3 ' UTR. Therefore, miR-497 can partially negatively regulate the activation of IRAK2-NF-kappa B pathway in LPS-induced inflammatory responses.
引用
收藏
页码:22874 / 22883
页数:10
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