首页> 外文期刊>Cytokine >Glutathione depletion is involved in the inhibition of procollagen alpha1(I) mRNA levels caused by TNF-alpha on hepatic stellate cells.
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Glutathione depletion is involved in the inhibition of procollagen alpha1(I) mRNA levels caused by TNF-alpha on hepatic stellate cells.

机译:谷胱甘肽耗竭参与抑制肝星状细胞上由TNF-α引起的原胶原α1(I)mRNA水平。

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摘要

TNF-alpha has been shown to inhibit procollagen alpha1(I) expression in hepatic stellate cells (HSC), although the molecular mechanisms involved have not been fully established. In the present work, we studied the possible role played by oxidative stress and NFkappaB on the antifibrogenic action of TNF-alpha on a cell line of rat HSC. Treatment of HSC with TNF-alpha did not affect either intracellular levels of reactive oxygen species or lipid peroxidation, but caused a decrease on reduced glutathione (GSH) levels. Restoration of intracellular GSH by incubation with exogenous GSH prevented the inhibition of procollagen alpha1(I) levels caused by TNF-alpha. The effect of GSH was not mimicked by antioxidants like deferoxamine, tempol or trolox. Activation of NFkappaB by TNF-alpha was also abolished by preincubation of HSC with GSH, but not by deferoxamine, tempol or trolox. These results point to GSH depletion as a mediator of TNF-alpha action in HSC.
机译:TNF-α已显示抑制肝星状细胞(HSC)中的原胶原α1(I)表达,尽管所涉及的分子机制尚未完全确立。在本工作中,我们研究了氧化应激和NFkappaB对TNF-α对大鼠HSC细胞系的抗纤维化作用的可能作用。用TNF-α治疗HSC不会影响细胞内活性氧水平或脂质过氧化作用,但会导致降低的谷胱甘肽(GSH)水平降低。通过与外源GSH孵育来恢复细胞内GSH可以防止抑制由TNF-α引起的原胶原α1(I)水平。抗氧化剂如去铁胺,tempol或trolox不能模仿GSH的作用。 HSC与GSH的预温育也消除了TNF-α对NFkappaB的激活,但去铁敏,tempol或trolox却没有。这些结果表明,GSH耗竭是HSC中TNF-α作用的介质。

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