1. Academic Validation
  2. A phycocyanin derived eicosapeptide attenuates lung fibrosis development

A phycocyanin derived eicosapeptide attenuates lung fibrosis development

  • Eur J Pharmacol. 2021 Oct 5;908:174356. doi: 10.1016/j.ejphar.2021.174356.
Qihao Li 1 Wen Peng 1 Zhaoyu Zhang 1 Xin Pei 1 Zhongkan Sun 1 Yu Ou 2
Affiliations

Affiliations

  • 1 School of Life Science and Technology, China Pharmaceutical University, 639 Longmian Avenue, Nanjing, 211198, China.
  • 2 School of Life Science and Technology, China Pharmaceutical University, 639 Longmian Avenue, Nanjing, 211198, China. Electronic address: [email protected].
Abstract

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.

Keywords

Epithelial-mesenchymal transition (EMT); MAPKs; Phycocyanin derived eicosapeptide (PP20); Pulmonary fibrosis; TGF-β1/Smad.

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