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Epigenetic reader MeCP2 repressed WIF1 boosts lung fibroblast proliferation, migration and pulmonary fibrosis.
- Source :
-
Toxicology letters [Toxicol Lett] 2023 May 15; Vol. 381, pp. 1-12. Date of Electronic Publication: 2023 Apr 13. - Publication Year :
- 2023
-
Abstract
- Epigenetic has been implicated in pulmonary fibrosis. However, there is limited information regarding the biological role of the epigenetic reader MeCP2 in pulmonary fibrosis. The aim of this study was to investigate the role of MeCP2 and its target WIF1 in pulmonary fibrosis. The pathological changes and collagen depositions was analyzed by H&E, Masson's Trichrome Staining and Sirius Red staining. MeCP2, WIF1, α-SMA, Wnt1, β-catenin, and collagen I expression were analyzed by western blotting, RT-qPCR, immunohistochemistry, immunofluorescence, respectively. The effects of MeCP2 on pulmonary fibrosis involve epigenetic mechanisms, using cultured cells, animal models, and clinical samples. Herein, our results indicated that MeCP2 level was up-regulated, while WIF1 was decreased in Bleomycin (BLM)-induced mice pulmonary fibrosis tissues, patients pulmonary fibrosis tissues and TGF-β1-induced lung fibroblast. Knockdown of MeCP2 by siRNA can rescue WIF1 downregulation in TGF-β1-induced lung fibroblast, inhibited lung fibroblast activation. The DNA methylation inhibitor 5-azadC-treated lung fibroblasts have increased WIF1 expression with reduced MeCP2 association. In addition, we found that reduced expression of WIF1 caused by TGF-β1 is associated with the promoter methylation status of WIF1. Moreover, in vivo studies revealed that knockdown of MeCP2 mice exhibited significantly ameliorated pulmonary fibrosis, decreased interstitial collagen deposition, and increased WIF1 expression. Taken together, our study showed that epigenetic reader MeCP2 repressed WIF1 facilitates lung fibroblast proliferation, migration and pulmonary fibrosis.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2023 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Mice
Bleomycin toxicity
Cell Proliferation
Collagen metabolism
Epigenesis, Genetic
Fibroblasts
Lung
Transforming Growth Factor beta1 metabolism
Methyl-CpG-Binding Protein 2 genetics
Methyl-CpG-Binding Protein 2 metabolism
Methyl-CpG-Binding Protein 2 pharmacology
Pulmonary Fibrosis chemically induced
Pulmonary Fibrosis genetics
Pulmonary Fibrosis pathology
Adaptor Proteins, Signal Transducing metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1879-3169
- Volume :
- 381
- Database :
- MEDLINE
- Journal :
- Toxicology letters
- Publication Type :
- Academic Journal
- Accession number :
- 37061208
- Full Text :
- https://doi.org/10.1016/j.toxlet.2023.04.004