School of Life Science and Technology, China Pharmaceutical University, 639 Longmian Avenue, Nanjing, 211198, China.
School of Life Science and Technology, China Pharmaceutical University, 639 Longmian Avenue, Nanjing, 211198, China.
Eur J Pharmacol. 2021 Oct 5;908:174356. doi: 10.1016/j.ejphar.2021.174356. Epub 2021 Jul 16.
Pulmonary fibrosis (PF) is a progressive respiratory disease. Phycocyanin derived eicosapeptide (PP20) is a novel peptide derived from active protein C-phycocyanin in Cyanobacteria. The aim of our study was to explore the anti-fibrotic activity of the PP20 and its underlying mechanism. Characteristic features of pulmonary fibrosis in oleic acid (OA)-induced mice and epithelial-mesenchymal transition (EMT) in TGF-β1-exposed A549 and HFL-1 cells with or without PP20 and the change of TGF-β/Smad and MAPK signaling pathways were examined. Smad and MAPK agonists were used to explore the role of TGF-β/Smad and MAPK signaling in TGF-β1- induced collagen I expression in A549 cells and α-SMA expression in HFL-1 cells when treated with PP20. Our results showed that PP20 significantly alleviated the inflammatory response and tissue destruction, inhibited EMT, restored the imbalance of TIMP-1/MMP-9 and reduced collagen fiber deposition. Moreover, PP20 inhibited TGF-β1-induced EMT and collagen I expression in A549 cells. PP20 could also inhibit the proliferation, and decrease TGF-β1-induced the expression of collagen I and transformation of fibroblasts into myofibroblasts in HFL-1 cells. Additionally, animal experiments and cell experiments combined with pathway agonists have shown that PP20 can negatively regulate TGF-β/Smad and MAPK pathways and show anti-fibrotic properties. PP20 may be a promising drug candidate for protection against pulmonary fibrosis.
肺纤维化(PF)是一种进行性呼吸系统疾病。藻蓝蛋白衍生二十肽(PP20)是一种从蓝藻活性蛋白 C-藻蓝蛋白中衍生的新型肽。我们的研究旨在探讨 PP20 的抗纤维化活性及其潜在机制。研究考察了油酸(OA)诱导的小鼠肺纤维化特征、TGF-β1 暴露的 A549 和 HFL-1 细胞中的上皮-间充质转化(EMT)以及 TGF-β/Smad 和 MAPK 信号通路的变化,并用 PP20 进行了处理。用 Smad 和 MAPK 激动剂研究了 TGF-β/Smad 和 MAPK 信号通路在 TGF-β1 诱导 A549 细胞中胶原 I 表达和 HFL-1 细胞中 α-SMA 表达时,PP20 处理的作用。结果表明,PP20 显著减轻了炎症反应和组织破坏,抑制了 EMT,恢复了 TIMP-1/MMP-9 的失衡,减少了胶原纤维沉积。此外,PP20 抑制了 TGF-β1 诱导的 A549 细胞 EMT 和胶原 I 表达。PP20 还可以抑制 HFL-1 细胞的增殖,并降低 TGF-β1 诱导的胶原 I 表达和纤维母细胞向肌成纤维细胞的转化。此外,动物实验和细胞实验结合通路激动剂表明,PP20 可以负调控 TGF-β/Smad 和 MAPK 通路,具有抗纤维化特性。PP20 可能是一种有前途的抗肺纤维化药物候选物。