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

被引:29
|
作者
Li, Se-Ruo [1 ]
Tan, Zhu-Xia [1 ]
Chen, Yuan-Hua [2 ]
Hu, Biao [1 ]
Zhang, Cheng [2 ]
Wang, Hua [2 ]
Zhao, Hui [1 ]
Xu, De-Xiang [2 ]
机构
[1] Anhui Med Univ, Affiliated Hosp 2, Hefei 230032, Anhui, Peoples R China
[2] Anhui Med Univ, Dept Toxicol, 81 Meishan Rd, Hefei 230032, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Pulmonary fibrosis; Vitamin D deficiency; Epithelial-mesenchymal transition; Bleomycin; Mice; COGNITIVE DECLINE; PATHOGENESIS; INHIBITION; INJURY; RISK;
D O I
10.1186/s12931-019-1232-6
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
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-beta)/Smad3 signaling was evaluated in the lungs of BLM-treated mice. Results The relative weight of lungs was elevated in BLM-treated mice. Col1 alpha 1 and Col1 alpha 2, 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 alpha-SMA, two EMT markers, were upregulated in the lungs of BLM-treated mice. Pulmonary TGF-beta/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-beta/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-beta/Smad2/3 activation and subsequent EMT in BLM-induced lung fibrosis. Conclusion Vitamin D deficiency exacerbates BLM-induced pulmonary fibrosis partially through aggravating TGF-beta/Smad2/3-mediated EMT in the lungs.
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页数:11
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