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Insulin-like growth factor-1 isoforms in rat hepatocytes and cholangiocytes and their involvement in protection against cholestatic injury

机译:大鼠肝细胞和胆管细胞中胰岛素样生长因子-1同工型及其参与胆汁淤积性损伤的保护作用

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摘要

A ‘locally acting’ IGF1 (insulin-like growth factor 1) isoform has been recently identified in the skeletal muscle and neural tissues where it accelerates injury repair. No information exist on the expression and function of IGF1 isoforms in the liver. We investigated IGF1 isoforms in rat hepatocytes and cholangiocytes and evaluated their involvement in cell proliferation or damage induced by experimental cholestasis (bile duct ligation, BDL) or hydrophobic bile salts. IGF1 isoforms were analyzed by real-time PCR by using β-actin as internal reference. In both hepatocytes and cholangiocytes, the ‘locally acting’ IGF1 isoform (XO6108) and ‘circulating’ IGF1 isoform () represented respectively 44 and 52% of the total IGF1. Basal mRNAs for both ‘locally acting’ and ‘circulating’ IGF1 isoforms were higher (P < 0.05) in hepatocytes than cholangiocytes. After BDL for 3 h, the ‘locally acting’ IGF1 isoform decreased threefold (P < 0.05) in hepatocytes but remained stable in cholangiocytes with respect to sham-controls. After 1 week of BDL, hepatocytes displayed a further fivefold decrease of ‘locally acting’ IGF1 mRNA. In contrast, cholangiocytes showed an eightfold increase of the ‘locally acting’ IGF1 mRNA. The effect of 3 h of BDL on IGF1 isoforms was reproduced in vitro by incubation with glycochenodeoxycholate (GCDC). The cytotoxic effects (inhibition of proliferation and induction of apoptosis) of GCDC on isolated cholangiocytes were more pronounced after selective silencing (SiRNA) of ‘locally acting’ than ‘circulating’ IGF1 isoform. Rat hepatocytes and cholangiocytes express the ‘locally acting’ IGF1 isoform, which decreased during cell damage and increased during cell proliferation. The ‘locally acting’ IGF1 was more active than the ‘circulating’ isoform in protecting cholangiocytes from GCDC-induced cytotoxicity. These findings indicate that, besides muscle and neural tissues, also in liver cells the ‘locally acting’ IGF1 isoform is important in modulating response to damage.
机译:最近在骨骼肌和神经组织中发现了一种“局部作用”的IGF1(胰岛素样生长因子1)同工型,可促进损伤修复。没有关于IGF1亚型在肝脏中表达和功能的信息。我们研究了大鼠肝细胞和胆管细胞中的IGF1亚型,并评估了它们参与实验性胆汁淤积症(胆管结扎,BDL)或疏水性胆汁盐诱导的细胞增殖或损伤。使用β-肌动蛋白作为内部参考,通过实时PCR分析IGF1亚型。在肝细胞和胆管细胞中,“局部作用” IGF1亚型(XO6108)和“循环” IGF1亚型()分别占总IGF1的44%和52%。肝细胞中“局部作用”和“循环” IGF1亚型的基础mRNA均高于胆管细胞(P <0.05)。 BDL 3 h后,相对于假对照组,“局部作用” IGF1亚型在肝细胞中下降了三倍(P <0.05),但在胆管细胞中保持稳定。 BDL 1周后,肝细胞的“局部作用” IGF1 mRNA进一步降低了五倍。相反,胆管细胞显示“局部作用” IGF1 mRNA增加了八倍。通过与糖去氧胆酸(GCDC)孵育,在体外重现了3小时的BDL对IGF1亚型的影响。在选择性沉默(SiRNA)为“局部作用”后,GCDC对分离的胆管细胞的细胞毒性作用(抑制增殖和诱导凋亡)比“循环” IGF1亚型更为明显。大鼠肝细胞和胆管细胞表达“局部作用” IGF1亚型,该亚型在细胞损伤期间减少而在细胞增殖期间增加。在保护胆管细胞免受GCDC诱导的细胞毒性作用方面,“局部作用” IGF1比“循环”同工型更具活性。这些发现表明,除了肌肉和神经组织外,在肝细胞中,“局部作用” IGF1亚型在调节对损伤的反应中也很重要。

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