Department of Respiratory Medicine, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, P.R. China.
Department of Respiratory Medicine, Yantai Yuhuangding Hospital, Yantai, Shandong 264000, P.R. China.
Mol Med Rep. 2019 Apr;19(4):2869-2875. doi: 10.3892/mmr.2019.9900. Epub 2019 Jan 28.
The aim of the present study was to investigate whether the expression of tribbles pseudokinase 3 (TRB3) is involved in pulmonary interstitial fibrosis and to examine the possible mechanisms. The expression of TRB3 in murine alveolar type II epithelial cells (MLE‑12 cells) following transforming growth factor β1 (TGF‑β1) stimulation was assessed using various techniques, including western blot and reverse transcription‑quantitative polymerase chain reaction assays. TRB3 overexpression and downregulation models were used to evaluate the impact of TRB3 on the TGF‑β1‑induced epithelial‑mesenchymal transition (EMT) of MLE‑12 cells. The downregulation of TRB3 was induced by RNA interference. The expression of TRB3 was significantly increased in MLE‑12 cells following the activation of TGF‑β1 (P<0.05). The overexpression of TRB3 was found to promote activation of the TGF‑β1/Smad3 signaling pathway, EMT, and the upregulated expression of β‑catenin and EMT‑related genes and proteins (P<0.05), whereas the downregulation of TRB3 attenuated the promoting effect on EMT induced by TGF‑β1. In addition, the overexpression of TRB3 inhibited MLE‑12 cell proliferation by stimulating apoptosis, leading to the formation of pulmonary fibrosis (PF). The positive feedback loop demonstrated that TGF‑β1 induced the expression of TRB3, and TRB3, in turn, stimulated EMT and promoted the onset of PF through activation of the TGF‑β1/Smad3 signaling pathway. Therefore, TRB3 may promote the formation of PF through the TGF‑β1/Smad3 signaling pathway.
本研究旨在探讨 tribbles 假激酶 3(TRB3)的表达是否参与肺间质纤维化,并探讨可能的机制。采用 Western blot 和逆转录-定量聚合酶链反应检测转化生长因子-β1(TGF-β1)刺激后鼠肺泡Ⅱ型上皮细胞(MLE-12 细胞)中 TRB3 的表达。采用 TRB3 过表达和下调模型评估 TRB3 对 TGF-β1 诱导的 MLE-12 细胞上皮-间充质转化(EMT)的影响。通过 RNA 干扰下调 TRB3 的表达。TGF-β1 激活后 MLE-12 细胞中 TRB3 的表达明显增加(P<0.05)。TRB3 的过表达促进了 TGF-β1/Smad3 信号通路的激活、EMT 的发生以及β-连环蛋白和 EMT 相关基因和蛋白的上调表达(P<0.05),而 TRB3 的下调则减弱了 TGF-β1 诱导的 EMT 的促进作用。此外,TRB3 通过刺激细胞凋亡促进 MLE-12 细胞增殖,导致肺纤维化(PF)的形成。正反馈回路表明,TGF-β1 诱导 TRB3 的表达,而 TRB3 反过来通过激活 TGF-β1/Smad3 信号通路刺激 EMT 并促进 PF 的发生。因此,TRB3 可能通过 TGF-β1/Smad3 信号通路促进 PF 的形成。