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Hypoxia induces the activation of human hepatic stellate cells LX-2 through TGF-beta signaling pathway
Authors:Shi Yue-Feng  Fong Chi-Chun  Zhang Qi  Cheung Pik-Yuen  Tzang Chi-Hung  Wu Rudolf S S  Yang Mengsu
Institution:Department of Biology and Chemistry, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong, China.
Abstract: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.
Keywords:HSCs  hepatic stellate cells  TGF-β1  transforming growth factor-β1  ECM  extracellular matrix  MMP  metalloproteinase  TIMP  tissue inhibitor of metalloproteinase
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