EGCG induces β-defensin 3 against influenza A virus H1N1 by the MAPK signaling pathway

被引:21
作者
Mou, Qiuju [1 ]
Jiang, Yan [2 ]
Zhu, Lili [3 ]
Zhu, Zixin [4 ]
Ren, Tingting [5 ]
机构
[1] Guizhou Med Univ, Dept Blood Transfus, Affiliated Baiyun Hosp, Guiyang 550014, Guizhou, Peoples R China
[2] Guizhou Med Univ, Dept Microbiol, Affiliated Hosp, Guiyang 550004, Guizhou, Peoples R China
[3] Guizhou Med Univ, Dept Blood Transfus, Affiliated Hosp, Guiyang 550004, Guizhou, Peoples R China
[4] Guizhou Med Univ, Sch Basic Med Sci, Guiyang 550025, Guizhou, Peoples R China
[5] Guizhou Med Univ, Dept Physiol Chem, Affiliated Hosp, 19 Beijing St, Guiyang 550004, Guizhou, Peoples R China
基金
中国国家自然科学基金;
关键词
EGCG; beta-defensin; 3; H1N1; MAPK signaling pathway; P38; MAPK; EXPRESSION; CELLS; INHIBITION; RECEPTOR;
D O I
10.3892/etm.2020.9047
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Epigallocatechin gallate (EGCG) is the main component of green tea, which has been proven to inhibit a variety of viruses, including influenza A virus. However, the mechanism of EGCG against influenza virus remains to be further explored. The mechanism of EGCG against influenza virus was studied. The results showed that EGCG significantly increased the levels of HBD3 mRNA and protein, while the levels of phosphorylation of (p)-p38 MAPK, ERK and JNK after EGCG treatment were significantly up-regulated. p38 MAPK, ERK and JNK inhibitors significantly inhibited the expression of HBD3 induced by EGCG. On the other hand, EGCG significantly inhibited the expression of HA and NP proteins in influenza A virus H1N1, but attenuated the anti-influenza A virus effect of EGCG after silencing HBD3. Thus, the anti-influenza virus effect of EGCG is related to the induction of HBD3 expression. In addition, the expression of EGCG-induced HBD3 is related to the p38 MAPK, ERK and JNK signaling pathways. The research data show that EGCG can induce HBD3 expression through p38 MAPK, ERK and JNK signaling pathway to inhibit the replication of influenza A virus H1N1, providing a new and effective candidate drug for influenza virus.
引用
收藏
页码:3017 / 3024
页数:8
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