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首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >Parathyroid hormone-related protein activates HSCs via hedgehog signalling during liver fibrosis development
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Parathyroid hormone-related protein activates HSCs via hedgehog signalling during liver fibrosis development

机译:甲状旁腺激素相关蛋白在肝纤维化发展过程中通过刺猬信号激活HSC

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摘要

Recently, we showed that parathyroid hormone-like hormone (PTHLH), a cytokine-like polyprotein, is critical for extracellular matrix (ECM) deposition through the activation of hepatic stellate cells (HSCs). Here, we show that N-terminal PTHLH is secreted into the supernatant of injured hepatocytes, its expression is positively correlated with liver fibrosis severity based on mice liver biopsies, and it is primarily expressed in the cytoplasm of hepatocytes along the fibrous septa of fibrotic livers. PTHLH overexpression in mice was achieved through adeno-associated virus-mediated gene delivery (AAV9-PTHLH), and liver fibrosis was induced with carbon tetrachloride (CCl 4 ). We observed that AAV9-PTHLH induced spontaneous development of liver fibrosis and increased sensitivity to CCl 4 . PTHLH increased Hedgehog (Hh) pathway activation in a PTH1R-dependent manner, and the effect of PTHLH was primarily mediated by protein kinase C (PKC) θ . PTHLH-mediated PTH1R-PKC θ pathway activation is a key event in the profibrotic Hh-dependent activation of HSCs.
机译:最近,我们发现甲状旁腺激素样激素(PTHLH)是一种细胞因子样多蛋白,通过激活肝星状细胞(HSC)对于细胞外基质(ECM)沉积至关重要。在这里,我们显示N末端PTHLH分泌到受损肝细胞的上清液中,其表达与小鼠肝活检的肝纤维化严重程度呈正相关,并且主要在沿肝纤维化纤维膜的肝细胞的细胞质中表达。 。通过腺相关病毒介导的基因传递(AAV9-PTHLH)实现了小鼠PTHLH的过表达,并用四氯化碳(CCl 4)诱导了肝纤维化。我们观察到AAV9-PTHLH诱导肝纤维化的自发发展,并增加了对CCl 4的敏感性。 PTHLH以PTH1R依赖性方式增加了Hedgehog(Hh)通路的激活,并且PTHLH的作用主要由蛋白激酶C(PKC)θ介导。 PTHLH介导的PTH1R-PKCθ途径激活是HSC的纤维化Hh依赖性激活中的关键事件。

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