ReferenceID 6196

Scutellarin ameliorates pulmonary fibrosis through inhibiting NF-κB/NLRP3-mediated epithelial-mesenchymal transition and inflammation

Cell Death Dis

Idiopathic pulmonary fibrosis (IPF) is featured with inflammation and extensive lung remodeling caused by overloaded deposition of extracellular matrix. Scutellarin is the major effective ingredient of breviscapine and i

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Reference Id
6196
Evidence Id
22786
Core Evidence Id
22786
Source Reference Id
5664
Herb2 Reference Id
HBREF006461
Subject Paper Key
HBIN043533_33188176
Pubmed Id
33188176
Doi
10.1038/s41419-020-03178-2
Paper Title
Scutellarin ameliorates pulmonary fibrosis through inhibiting NF-κB/NLRP3-mediated epithelial-mesenchymal transition and inflammation
Paper Abstract
Idiopathic pulmonary fibrosis (IPF) is featured with inflammation and extensive lung remodeling caused by overloaded deposition of extracellular matrix. Scutellarin is the major effective ingredient of breviscapine and its anti-inflammation efficacy has been reported before. Nevertheless, the impact of scutellarin on IPF and the downstream molecular mechanism remain unclear. In this study, scutellarin suppressed BLM-induced inflammation via NF-kappaB/NLRP3 pathway both in vivo and in vitro. BLM significantly elevated p-p65/p65 ratio, IkappaBalpha degradation, and levels of NLRP3, caspase-1, caspase-11, ASC, GSDMDNterm, IL-1beta, and IL-18, while scutellarin reversed the above alterations except for that of caspase-11. Scutellarin inhibited BLM-induced epithelial-mesenchymal transition (EMT) process in vivo and in vitro. The expression levels of EMT-related markers, including fibronectin, vimentin, N-cadherin, matrix metalloproteinase 2 (MMP-2) and MMP-9, were increased in BLM group, and suppressed by scutellarin. The expression level of E-cadherin showed the opposite changes. However, overexpression of NLRP3 eliminated the anti-inflammation and anti-EMT functions of scutellarin in vitro. In conclusion, scutellarin suppressed inflammation and EMT in BLM-induced pulmonary fibrosis through NF-kappaB/NLRP3 signaling.
Journal
Cell Death Dis
Publish Year
2020
Experiment Subject
Experiment Type
Cell Experiment
Phenotype Related
Idiopathic Pulmonary Fibrosis; Pulmonary Fibrosis; Inflammation
Paper Title Cn
Paper Title En
Scutellarin ameliorates pulmonary fibrosis through inhibiting NF-κB/NLRP3-mediated epithelial-mesenchymal transition and inflammation
Bilingual Status
semi_complete