A phycocyanin derived eicosapeptide attenuates lung fibrosis development.

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

Journal

European journal of pharmacology
ISSN: 1879-0712
Titre abrégé: Eur J Pharmacol
Pays: Netherlands
ID NLM: 1254354

Informations de publication

Date de publication:
05 Oct 2021
Historique:
received: 23 05 2021
revised: 23 06 2021
accepted: 15 07 2021
pubmed: 20 7 2021
medline: 8 1 2022
entrez: 19 7 2021
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 34280398
pii: S0014-2999(21)00509-4
doi: 10.1016/j.ejphar.2021.174356
pii:
doi:

Substances chimiques

TGFB1 protein, human 0
Transforming Growth Factor beta1 0
Phycocyanin 11016-15-2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

174356

Informations de copyright

Copyright © 2021. Published by Elsevier B.V.

Auteurs

Qihao Li (Q)

School of Life Science and Technology, China Pharmaceutical University, 639 Longmian Avenue, Nanjing, 211198, China.

Wen Peng (W)

School of Life Science and Technology, China Pharmaceutical University, 639 Longmian Avenue, Nanjing, 211198, China.

Zhaoyu Zhang (Z)

School of Life Science and Technology, China Pharmaceutical University, 639 Longmian Avenue, Nanjing, 211198, China.

Xin Pei (X)

School of Life Science and Technology, China Pharmaceutical University, 639 Longmian Avenue, Nanjing, 211198, China.

Zhongkan Sun (Z)

School of Life Science and Technology, China Pharmaceutical University, 639 Longmian Avenue, Nanjing, 211198, China.

Yu Ou (Y)

School of Life Science and Technology, China Pharmaceutical University, 639 Longmian Avenue, Nanjing, 211198, China. Electronic address: ouyu2008@126.com.

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Classifications MeSH