首页> 外文期刊>FEBS Letters >p38 MAPK mediates the regulation of α1(I) procollagen mRNA levels by TNF‐α and TGF‐β in a cell line of rat hepatic stellate cells
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p38 MAPK mediates the regulation of α1(I) procollagen mRNA levels by TNF‐α and TGF‐β in a cell line of rat hepatic stellate cells

机译:p38 MAPK介导大鼠肝星状细胞细胞系中TNF-α和TGF-β对α1(I)胶原蛋白mRNA水平的调节

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>The role of members of the mitogen-activated protein kinase (MAPK) family on tumor necrosis factor α (TNF-α)-mediated down-regulation of col1a1 gene was studied. TNF-α increased extracellular-regulated kinase and Jun-N-terminal kinase phosphorylation, but these effects were not related to its inhibitory effect on α1(I) procollagen (col1a1) mRNA levels. Phosphorylation of p38 MAPK was decreased in response to TNF-α, and the specific p38 MAPK inhibitor SB203580 mimicked the effect of TNF-α on col1a1 mRNA levels. Transforming growth factor β (TGF-β) increased p38 MAPK phosphorylation and SB203580 prevented the induction of col1a1 mRNA levels by TGF-β. These results suggest that p38 MAPK plays an important role in regulating the expression of col1a1 in hepatic stellate cells in response to cytokines.
机译:>研究了丝裂原活化蛋白激酶(MAPK)家族成员在肿瘤坏死因子α(TNF-α)介导的col1a1基因下调中的作用。 TNF-α增加了细胞外调节激酶和Jun-N-末端激酶的磷酸化,但这些作用与其对α1(I)前胶原(col1a1)mRNA水平的抑制作用无关。 p38 MAPK的磷酸化响应TNF-α而降低,并且特定的p38 MAPK抑制剂SB203580模仿了TNF-α对col1a1 mRNA水平的影响。转化生长因子β(TGF-β)增加p38 MAPK磷酸化,SB203580阻止TGF-β诱导col1a1 mRNA水平。这些结果表明,p38 MAPK在调节肝星状细胞对细胞因子的应答中对col1a1表达的调节中起着重要作用。

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