Schistosoma japonicum protein SjP40 inhibits TGF-β1-induced activation of hepatic stellate cells

被引:0
作者
Xiaolei Sun
Lingbo Zhang
Jianxin Wang
Jinling Chen
Dandan Zhu
Pei Shen
Xue He
Jing Pan
Wenxia Peng
Yinong Duan
机构
[1] Nantong University,Department of Pathogen Biology, School of Medicine
[2] Affiliated Hospital of Nantong University,Laboratory Medicine Center
[3] Jiangsu University,School of Medical Science and Laboratory Medicine
[4] the Second Affiliated Hospital of Nanjing Medical University,Department of Pathology
来源
Parasitology Research | 2015年 / 114卷
关键词
P40; Hepatic stellate cells; Hepatic fibrosis; TGF-β1; ERK;
D O I
暂无
中图分类号
学科分类号
摘要
SjP40 is a major egg antigen of Schistosoma japonicum. In the present study, the authors investigated the effect of SjP40 in vitro on transforming growth factor-β1 (TGF-β1)- stimulated hepatic stellate cells (HSCs). LX-2, an immortalized human HSC line, was treated with purified recombinant SjP40 (rSjP40) in the presence or absence of TGF-β1. Quantitative real-time polymerase chain reaction and western blot analysis were performed to determine messenger ribonucleic acid and protein of fibrogenic genes and TGF-β signaling pathway. The results showed that expression of fibrogenic genes was significantly reduced by rSjP40. Furthermore, rSjP40 also suppressed the TGF-β1-induced upregulation of Smads and ERK proteins. We also found that the effect of rSjP40 on HSCs was similar to SB431542, an inhibitor of type I TGF-β receptor. In conclusion, the data suggest that SjP40 attenuates HSC activation, which might be, at least in part, mediated by inhibiting the TGF-β and ERK signaling pathways.
引用
收藏
页码:4251 / 4257
页数:6
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