首页> 美国卫生研究院文献>Molecular Medicine Reports >Effect of Yi Guan Jian decoction on differentiation of bone marrow mesenchymalstem cells into hepatocyte-like cells in dimethylnitrosamine-induced liver cirrhosis in mice
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Effect of Yi Guan Jian decoction on differentiation of bone marrow mesenchymalstem cells into hepatocyte-like cells in dimethylnitrosamine-induced liver cirrhosis in mice

机译:益官健汤对二甲基亚硝胺诱导的肝硬化小鼠骨髓间充质干细胞向肝样细胞分化的影响

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摘要

Yi Guan Jian decoction (YGD) may induce the differentiation of bone marrow mesenchymal stem cells (BMSCs) into hepatocyte-like cells (HLCs); however, the underlying mechanisms remain to be elucidated. The present study aimed to investigate this process. To do this, a dimethylnitrosamine (DMN)-induced liver cirrhosis mouse model was established. The mice from the model group were randomly divided into three subgroups: i) Negative control, ii) hepatocyte growth factor and iii) YGD. The overall health, liver function and histological alterations were monitored. The expression of α-smooth muscle actin (α-SMA), C-X-C chemokine receptor type 4 (CXCR4), extracellular signal-regulated kinase (ERK1/2), nuclear factor κB p65 subunit (NF-κB p65) and β-catenin were measured by immunohistochemistry, western blotting and reverse transcription-quantitative polymerase chain reaction. Following administration of DMN, the overall health of the mice significantly decreased, with an increase in pathological developments and liver damage resulting in a decrease in liver function. Immunohistochemistry revealed that the expression of α-SMA, CXCR4, ERK1/2, NF-κB p65 and β-catenin was upregulated. Following treatment with YGD, the overall health, liver function and pathology improved. The mRNA and protein expression levels of CXCR4 and ERK1/2 were upregulated, where as α-SMA, NF-κB p65 and β-catenin levels were downregulated. The results demonstrated that YGD may induce the differentiation of BMSCs into HLCs to reverse DMN-induced liver cirrhosis; this may be achieved via an upregulation of the SDF-1/CXCR4 axis to activate the mitogen activated protein kinase/ERK1/2 signaling pathway.
机译:益冠煎汤可诱导骨髓间充质干细胞向肝样细胞分化。但是,其潜在机制仍有待阐明。本研究旨在调查这一过程。为此,建立了二甲基亚硝胺(DMN)诱导的肝硬化小鼠模型。来自模型组的小鼠被随机分为三个亚组:i)阴性对照,ii)肝细胞生长因子和iii)YGD。监测整体健康,肝功能和组织学改变。 α-平滑肌肌动蛋白(α-SMA),4型CXC趋化因子受体(CXCR4),细胞外信号调节激酶(ERK1 / 2),核因子κBp65亚基(NF-κBp65)和β-catenin的表达分别为通过免疫组织化学,蛋白质印迹和逆转录定量聚合酶链反应检测。施用DMN后,小鼠的整体健康状况显着下降,病理发展和肝脏损害增加,导致肝功能下降。免疫组化显示α-SMA,CXCR4,ERK1 / 2,NF-κBp65和β-catenin的表达上调。用YGD治疗后,整体健康,肝功能和病理状况得到改善。 CXCR4和ERK1 / 2的mRNA和蛋白表达水平上调,而α-SMA,NF-κBp65和β-catenin水平下调。结果表明,YGD可能诱导骨髓间充质干细胞向HLCs分化,从而逆转DMN引起的肝硬化。这可以通过上调SDF-1 / CXCR4轴来激活有丝分裂原激活的蛋白激酶/ ERK1 / 2信号通路来实现。

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