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COPD 肺单核细胞中的 circRERE/miR-144-3p/TLR2/MMP9 信号轴促进肺上皮细胞的 EMT。

The circRERE/miR-144-3p/TLR2/MMP9 signaling axis in COPD pulmonary monocytes promotes the EMT of pulmonary epithelial cells.

机构信息

Department of Respiratory and Critical Care Medicine, General Hospital of Southern Theater Command of PLA, Guangzhou, China.

Graduate School, Guangzhou University of Chinese Medicine, Guangzhou, China.

出版信息

Biochem Biophys Res Commun. 2022 Oct 15;625:1-8. doi: 10.1016/j.bbrc.2022.07.119. Epub 2022 Aug 3.

Abstract

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.

摘要

慢性阻塞性肺疾病(COPD)严重威胁人类健康,但目前针对 COPD 的有效靶向治疗仍缺乏。在 COPD 的进展过程中,上皮间质转化(EMT)确保了肺上皮细胞的重塑,但由于其复杂而难以捉摸的机制,无法对其进行精确靶向治疗。在本研究中,我们确定 TLR2/MMP9 轴在香烟烟雾(CS)诱导的 COPD 小鼠肺单核细胞中上调。通过共培养系统,我们发现肺单核细胞中的 TLR2/MMP9 轴促进肺上皮细胞的 EMT。此外,我们的结果证实,miR-144-3p 通过直接结合 TLR2 的 3'UTR 抑制单核细胞中 TLR2 的表达。最后,我们证明 circRERE 作为海绵与 miR-144-3p 相互作用,从而促进单核细胞中 TLR2 的表达。因此,我们的研究结果表明,COPD 肺单核细胞中的 circRERE/miR-144-3p/TLR2/MMP9 轴在 CS 诱导的 COPD 中至关重要,circRERE 可能作为 COPD 的潜在治疗靶点。

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