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Differential expression of PTEN in hepatic tissue and hepatic stellate cells during rat liver fibrosis and its reversal

机译:大鼠肝纤维化过程中肝组织和肝星状细胞中PTEN的差异表达及其逆转

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To evaluate the change in phosphatase and tensin homology deleted on chromosome ten (PTEN) expression in liver fibrogenesis, particularly the reversal of fibrogenic liver tissues, and to investigate the relation with the proliferation and apoptosis of hepatic stellate cells (HSCs) in?vivo, a rat model of hepatic fibrosis was established by hypodermic injection of carbon tetrachloride (CCl4) mixed with olive oil at the concentration of 40% for 5?weeks (2?ml/kg, twice a week). Reversal of fibrosis was achieved with normal feedings for 4?weeks after CCl4 injection for 5?weeks. The expression of PTEN was measured by immunofluorescence, western blot analysis and real-time PCR. Co-expression of α-smooth muscle actin (α-SMA) with PTEN and α-SMA with terminal deoxynucleotidyltransferase-mediated dUTP nick end labelling (TUNEL) were assessed by confocal laser scanning microscopy. The results displayed that the expression of PTEN was reduced with fibrosis in both rat liver tissues and activated HSCs. By contrast, PTEN expression was increased with the reversal of liver fibrosis. Compared to the fibrogenic state, there were increased numbers of apoptotic activated HSCs during reversal of fibrosis. These data suggest that the dynamic expression of PTEN in rat liver tissues is negatively correlated with liver fibrosis and activated HSCs and is positively correlated with reversal of fibrosis and apoptotic activated HSCs. Modulation of PTEN expression may be an effective and novel method for the treatment of liver fibrosis.
机译:为了评估肝纤维化特别是肝纤维化肝组织逆转时,十号染色体(PTEN)表达上缺失的磷酸酶和张力蛋白同源性的变化,并研究其与肝星状细胞(HSC)增殖和凋亡的关系,通过皮下注射浓度为40%的橄榄油与四氯化碳(CCl4)混合皮下注射5?周(2?ml / kg,每周两次),建立了大鼠肝纤维化模型。注射CCl4 5周后,正常喂养4周可逆转纤维化。通过免疫荧光,蛋白质印迹分析和实时PCR测量PTEN的表达。通过共聚焦激光扫描显微镜评估了α-平滑肌肌动蛋白(α-SMA)与PTEN和α-SMA与末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)的共表达。结果表明,在肝组织和活化的HSCs中,PTEN的表达均随纤维化而降低。相比之下,PTEN表达随着肝纤维化的逆转而增加。与纤维化状态相比,在纤维化逆转期间凋亡激活的HSC数量增加。这些数据表明,PTEN在大鼠肝组织中的动态表达与肝纤维化和激活的HSC呈负相关,与与纤维化和凋亡激活的HSC的逆转呈正相关。 PTEN表达的调节可能是治疗肝纤维化的有效和新颖的方法。

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