单核细胞
肝细胞癌
乙型肝炎表面抗原
肝硬化
细胞因子
肝病
癌症研究
髓样
慢性肝病
肿瘤坏死因子α
免疫学
下调和上调
生物
受体
医学
乙型肝炎病毒
内科学
基因
病毒
生物化学
作者
Xiaojuan Wu,Bei Cai,Lu Wang,Yang Fu,Bin Wei,Qian Niu,Zhenzhen Su,Yamei Li,Lanlan Wang
标识
DOI:10.1016/j.clim.2020.108650
摘要
Abstract The triggering receptor expressed on myeloid cells-1 (TREM-1) signal is related to the continuous amplification of inflammatory pathway. However, it is not clear whether and how HBV can regulated the expression of TREM-1 on monocyte participated in the progression of liver disease. Here, we showed that the expression of TREM-1 on monocyte subsets were increased significantly in HBV related liver cirrhosis group compared with chronic infected group and healthy control group. HBsAg and HBeAg could up-regulated TREM-1 on monocyte by NF-KB pathway, and at least last for 72 h. Increased TREM-1 on monocyte might associated with high level of inflammatory cytokine (TNF-a, IL-1β and IL-6) and the activation of LX-2 cells. Bioinformatics analysis showed that the high expression of TREM-1 was related to the poor prognosis of hepatocellular carcinoma (HCC). The level of TREM-1 might help to predict the progression of HBV infected liver disease and treat target to prevent fibrosis progression.
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