TLR2型
慢性阻塞性肺病
MMP9公司
上皮-间质转换
下调和上调
医学
肺病
癌症研究
免疫学
炎症
化学
TLR4型
内科学
基因
生物化学
作者
Yongqiang Li,Xing Lü,Weifeng Li,Zhipeng Shi,Wei Du,Hong Xu,Zhifeng Liu,Yuting Wu
标识
DOI:10.1016/j.bbrc.2022.07.119
摘要
Chronic obstructive pulmonary disease (COPD) is a serious threat to human health, but an effective targeted therapy for COPD is still lacking at present. During the progression of COPD, the epithelial mesenchymal transition (EMT) ensures the remodeling of pulmonary epithelial cells, and it could not be precisely targeted due to its complex and elusive mechanism. In this study, we determined that the TLR2/MMP9 axis is upregulated in the pulmonary monocytes in cigarette smoke (CS)-induced COPD mice. Using a co-culture system, we identified that the TLR2/MMP9 axis in pulmonary monocytes promotes the EMT of pulmonary epithelial cells. Further, our results confirmed that miR-144-3p inhibits TLR2 expression in monocytes by directly binding to the 3'UTR of TLR2. Finally, we proved that circRERE works as a sponge to antagonize miR-144-3p and promote TLR2 expression in monocytes. Thus, our results conclude that the circRERE/miR-144-3p/TLR2/MMP9 axis in COPD pulmonary monocytes is critical for CS-induced COPD and circRERE may serve as a potential target for COPD.
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