Cargando…

Vitamin D deficiency exacerbates bleomycin-induced pulmonary fibrosis partially through aggravating TGF-β/Smad2/3-mediated epithelial-mesenchymal transition

BACKGROUND: Our earlier report indicated that active vitamin D3 inhibited epithelial-mesenchymal transition (EMT) in bleomycin (BLM)-induced pulmonary fibrosis. The objective of this study was to further investigate whether vitamin D deficiency exacerbates BLM-induced pulmonary fibrosis. METHODS: Th...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Se-Ruo, Tan, Zhu-Xia, Chen, Yuan-Hua, Hu, Biao, Zhang, Cheng, Wang, Hua, Zhao, Hui, Xu, De-Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882226/
https://www.ncbi.nlm.nih.gov/pubmed/31775746
http://dx.doi.org/10.1186/s12931-019-1232-6
_version_ 1783474110379065344
author Li, Se-Ruo
Tan, Zhu-Xia
Chen, Yuan-Hua
Hu, Biao
Zhang, Cheng
Wang, Hua
Zhao, Hui
Xu, De-Xiang
author_facet Li, Se-Ruo
Tan, Zhu-Xia
Chen, Yuan-Hua
Hu, Biao
Zhang, Cheng
Wang, Hua
Zhao, Hui
Xu, De-Xiang
author_sort Li, Se-Ruo
collection PubMed
description BACKGROUND: Our earlier report indicated that active vitamin D3 inhibited epithelial-mesenchymal transition (EMT) in bleomycin (BLM)-induced pulmonary fibrosis. The objective of this study was to further investigate whether vitamin D deficiency exacerbates BLM-induced pulmonary fibrosis. METHODS: This study consists of two independent experiments. Experiment 1, male mice were fed with vitamin D deficient (VDD) fodder. Experiment 2, Cyp27b1(+/+), Cyp27b1(+/−) and Cyp27b1(−/−) mice were fed with standard diet. For pulmonary fibrosis, mice were intratracheally instilled with a single dose of BLM (1.5 mg/kg). Serum 25(OH) D level was measured. Pulmonary collagen deposition was assessed by Sirius red staining. EMT was measured and transforming growth factor-beta (TGF-β)/Smad3 signaling was evaluated in the lungs of BLM-treated mice. RESULTS: The relative weight of lungs was elevated in BLM-treated mice. Col1α1 and Col1α2, two collagen protein genes, were upregulated, and collagen deposition, as determined by Sirius red staining, was observed in the lungs of BLM-treated mice. E-cadherin, an epithelial marker, was downregulated. By contrast, vimentin and α-SMA, two EMT markers, were upregulated in the lungs of BLM-treated mice. Pulmonary TGF-β/Smad3 signaling was activated in BLM-induced lung fibrosis. Further analysis showed that feeding VDD diet, leading to vitamin D deficiency, aggravated elevation of BLM-induced relative lung weight. Moreover, feeding VDD diet aggravated BLM-induced TGF-β/Smad3 activation and subsequent EMT in the lungs. In addition, feeding VDD diet exacerbated BLM-induced pulmonary fibrosis. Additional experiment showed that Cyp27b1 gene knockout, leading to active vitamin D3 deficiency, exacerbated BLM-induced pulmonary fibrosis. Moreover, Cyp27b1 gene knockout aggravated pulmonary TGF-β/Smad2/3 activation and subsequent EMT in BLM-induced lung fibrosis. CONCLUSION: Vitamin D deficiency exacerbates BLM-induced pulmonary fibrosis partially through aggravating TGF-β/Smad2/3-mediated EMT in the lungs.
format Online
Article
Text
id pubmed-6882226
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-68822262019-12-03 Vitamin D deficiency exacerbates bleomycin-induced pulmonary fibrosis partially through aggravating TGF-β/Smad2/3-mediated epithelial-mesenchymal transition Li, Se-Ruo Tan, Zhu-Xia Chen, Yuan-Hua Hu, Biao Zhang, Cheng Wang, Hua Zhao, Hui Xu, De-Xiang Respir Res Research BACKGROUND: Our earlier report indicated that active vitamin D3 inhibited epithelial-mesenchymal transition (EMT) in bleomycin (BLM)-induced pulmonary fibrosis. The objective of this study was to further investigate whether vitamin D deficiency exacerbates BLM-induced pulmonary fibrosis. METHODS: This study consists of two independent experiments. Experiment 1, male mice were fed with vitamin D deficient (VDD) fodder. Experiment 2, Cyp27b1(+/+), Cyp27b1(+/−) and Cyp27b1(−/−) mice were fed with standard diet. For pulmonary fibrosis, mice were intratracheally instilled with a single dose of BLM (1.5 mg/kg). Serum 25(OH) D level was measured. Pulmonary collagen deposition was assessed by Sirius red staining. EMT was measured and transforming growth factor-beta (TGF-β)/Smad3 signaling was evaluated in the lungs of BLM-treated mice. RESULTS: The relative weight of lungs was elevated in BLM-treated mice. Col1α1 and Col1α2, two collagen protein genes, were upregulated, and collagen deposition, as determined by Sirius red staining, was observed in the lungs of BLM-treated mice. E-cadherin, an epithelial marker, was downregulated. By contrast, vimentin and α-SMA, two EMT markers, were upregulated in the lungs of BLM-treated mice. Pulmonary TGF-β/Smad3 signaling was activated in BLM-induced lung fibrosis. Further analysis showed that feeding VDD diet, leading to vitamin D deficiency, aggravated elevation of BLM-induced relative lung weight. Moreover, feeding VDD diet aggravated BLM-induced TGF-β/Smad3 activation and subsequent EMT in the lungs. In addition, feeding VDD diet exacerbated BLM-induced pulmonary fibrosis. Additional experiment showed that Cyp27b1 gene knockout, leading to active vitamin D3 deficiency, exacerbated BLM-induced pulmonary fibrosis. Moreover, Cyp27b1 gene knockout aggravated pulmonary TGF-β/Smad2/3 activation and subsequent EMT in BLM-induced lung fibrosis. CONCLUSION: Vitamin D deficiency exacerbates BLM-induced pulmonary fibrosis partially through aggravating TGF-β/Smad2/3-mediated EMT in the lungs. BioMed Central 2019-11-27 2019 /pmc/articles/PMC6882226/ /pubmed/31775746 http://dx.doi.org/10.1186/s12931-019-1232-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Li, Se-Ruo
Tan, Zhu-Xia
Chen, Yuan-Hua
Hu, Biao
Zhang, Cheng
Wang, Hua
Zhao, Hui
Xu, De-Xiang
Vitamin D deficiency exacerbates bleomycin-induced pulmonary fibrosis partially through aggravating TGF-β/Smad2/3-mediated epithelial-mesenchymal transition
title Vitamin D deficiency exacerbates bleomycin-induced pulmonary fibrosis partially through aggravating TGF-β/Smad2/3-mediated epithelial-mesenchymal transition
title_full Vitamin D deficiency exacerbates bleomycin-induced pulmonary fibrosis partially through aggravating TGF-β/Smad2/3-mediated epithelial-mesenchymal transition
title_fullStr Vitamin D deficiency exacerbates bleomycin-induced pulmonary fibrosis partially through aggravating TGF-β/Smad2/3-mediated epithelial-mesenchymal transition
title_full_unstemmed Vitamin D deficiency exacerbates bleomycin-induced pulmonary fibrosis partially through aggravating TGF-β/Smad2/3-mediated epithelial-mesenchymal transition
title_short Vitamin D deficiency exacerbates bleomycin-induced pulmonary fibrosis partially through aggravating TGF-β/Smad2/3-mediated epithelial-mesenchymal transition
title_sort vitamin d deficiency exacerbates bleomycin-induced pulmonary fibrosis partially through aggravating tgf-β/smad2/3-mediated epithelial-mesenchymal transition
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882226/
https://www.ncbi.nlm.nih.gov/pubmed/31775746
http://dx.doi.org/10.1186/s12931-019-1232-6
work_keys_str_mv AT liseruo vitaminddeficiencyexacerbatesbleomycininducedpulmonaryfibrosispartiallythroughaggravatingtgfbsmad23mediatedepithelialmesenchymaltransition
AT tanzhuxia vitaminddeficiencyexacerbatesbleomycininducedpulmonaryfibrosispartiallythroughaggravatingtgfbsmad23mediatedepithelialmesenchymaltransition
AT chenyuanhua vitaminddeficiencyexacerbatesbleomycininducedpulmonaryfibrosispartiallythroughaggravatingtgfbsmad23mediatedepithelialmesenchymaltransition
AT hubiao vitaminddeficiencyexacerbatesbleomycininducedpulmonaryfibrosispartiallythroughaggravatingtgfbsmad23mediatedepithelialmesenchymaltransition
AT zhangcheng vitaminddeficiencyexacerbatesbleomycininducedpulmonaryfibrosispartiallythroughaggravatingtgfbsmad23mediatedepithelialmesenchymaltransition
AT wanghua vitaminddeficiencyexacerbatesbleomycininducedpulmonaryfibrosispartiallythroughaggravatingtgfbsmad23mediatedepithelialmesenchymaltransition
AT zhaohui vitaminddeficiencyexacerbatesbleomycininducedpulmonaryfibrosispartiallythroughaggravatingtgfbsmad23mediatedepithelialmesenchymaltransition
AT xudexiang vitaminddeficiencyexacerbatesbleomycininducedpulmonaryfibrosispartiallythroughaggravatingtgfbsmad23mediatedepithelialmesenchymaltransition