Trueperella pyogenes pyolysin inhibits lipopolysaccharide-induced inflammatory response in endometrium stromal cells via autophagy- and ATF6-dependent mechanism

被引:10
|
作者
Qi, Maozhen [1 ,2 ]
Liu, Jianguo [1 ,2 ]
Jiang, Qingran [1 ,2 ]
Niu, Hongyu [1 ,2 ]
Wang, Xinyu [1 ,2 ]
Zhou, Dong [1 ,2 ]
Lin, Pengfei [1 ,2 ]
Chen, Huatao [1 ,2 ]
Wang, Aihua [2 ,3 ]
Jin, Yaping [1 ,2 ]
机构
[1] Northwest A&F Univ, Coll Vet Med, Minist Agr, Key Lab Anim Biotechnol, Yangling 712100, Shaanxi, Peoples R China
[2] Northwest A&F Univ, Coll Vet Med, Dept Clin Vet Med, Yangling 712100, Shaanxi, Peoples R China
[3] Northwest A&F Univ, Coll Vet Med, Dept Prevent Vet Med, Yangling 712100, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Pyolysin; LPS; Costimulation; Autophagy; ATF6;
D O I
10.1007/s42770-021-00422-5
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Trueperella pyogenes (T. pyogenes) is a common opportunistic pathogen of many livestock and play an important regulation role during multibacterial infection and interaction with the host by its primary virulence factor pyolysin (PLO). The purpose of this study was to investigate the regulation role of PLO which serve as a combinational pathogen with lipopolysaccharide (LPS) during endometritis. In this study, the expression of bioactive recombinant PLO (rPLO) in a prokaryotic expression system and its purification are described. Moreover, we observed that rPLO inhibited the innate immune response triggered by LPS and that methyl-beta-cyclodextrin (MBCD) abrogated this inhibitory effect in goat endometrium stromal cells (gESCs). Additionally, we show from pharmacological and genetic studies that rPLO-induced autophagy represses gene expression by inhibiting NLRP3 inflammasome activation. Importantly, this study reported that ATF6 serves as a primary regulator of the cellular inflammatory reaction to rPLO. Overall, these observations suggest that T. pyogenes PLO could create an immunosuppressive environment for other pathogens invasion by regulating cellular signaling pathways.
引用
收藏
页码:939 / 952
页数:14
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