Vitamin D alleviates liver fibrosis by inhibiting histidine-rich calcium binding protein (HRC)

Liver fibrosis may progress toward cirrhosis and cancer without effective therapy. Here, we investigated the underlying mechanism of Vitamin D as a therapeutic approach. Carbon tetrachloride (CCL4)-induced mice model and transforming growth factor-β1 (TGF-β1) induced human hepatic stellate cell line...

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Veröffentlicht in:Chemico-biological interactions 2021-01, Vol.334, p.109355-109355, Article 109355
Hauptverfasser: Lu, Wanyi, Li, Xiaofeng, Liu, Ning, Zhang, Yalin, Li, Ye, Pan, Yiming, Yang, Jingxin, Liu, Zuwang, Kong, Juan
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Sprache:eng
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Zusammenfassung:Liver fibrosis may progress toward cirrhosis and cancer without effective therapy. Here, we investigated the underlying mechanism of Vitamin D as a therapeutic approach. Carbon tetrachloride (CCL4)-induced mice model and transforming growth factor-β1 (TGF-β1) induced human hepatic stellate cell line LX-2 were used in vivo and in vitro. The fibrotic profiles, degree of liver injury and HRC expression were assessed by histology, Western blot, immunohistochemistry and Real-Time PCR. The proliferation of cells transfected with HRC +/+ and HRC−/- plasmids was detected by MTS and cell cycle methods. Vitamin D significantly suppressed the expression of HRC in liver fibrosis model both in vivo and in vitro (P 
ISSN:0009-2797
1872-7786
DOI:10.1016/j.cbi.2020.109355