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首页> 外文期刊>FEBS letters. >Hypoxia induces the activation of human hepatic stellate cells LX-2 through TGF-beta signaling pathway.
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Hypoxia induces the activation of human hepatic stellate cells LX-2 through TGF-beta signaling pathway.

机译:缺氧通过TGF-β信号传导途径诱导人肝星状细胞LX-2活化。

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摘要

Hypoxia is a common environmental stress factor and is also associated with various physiological and pathological conditions such as fibrogenesis. The activation of hepatic stellate cells (HSCs) is the key event in the liver fibrogenesis. In this study, the behavior of human HSCs LX-2 in low oxygen tension (1% O2) was analyzed. Upon hypoxia, the expression of HIF-1alpha and VEGF gene was induced. The result of Western blotting showed that the expression of alpha-SMA was increased by hypoxic stimulation. Furthermore, the expression of MMP-2 and TIMP-1 genes was increased. Hypoxia also elevated the protein expression of the collagen type I in LX-2 cells. The analysis of TGF-beta/Smad signaling pathway showed that hypoxia potentiated the expression of TGF-beta1 and the phosphorylation status of Smad2. Gene expression profiles of LX-2 cells induced by hypoxia were obtained by using cDNA microarray technique.
机译:缺氧是一种常见的环境压力因素,还与各种生理和病理状况(如纤维生成)有关。肝星状细胞(HSC)的激活是肝纤维化的关键事件。在这项研究中,分析了人类HSC LX-2在低氧张力(1%O2)下的行为。缺氧时,诱导HIF-1α和VEGF基因的表达。 Western印迹的结果表明,低氧刺激增加了α-SMA的表达。此外,MMP-2和TIMP-1基因的表达增加。缺氧还提高了LX-2细胞中I型胶原蛋白的蛋白表达。 TGF-β/ Smad信号通路的分析表明,低氧增强了TGF-β1的表达和Smad2的磷酸化状态。利用cDNA微阵列技术获得了缺氧诱导的LX-2细胞的基因表达谱。

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