首页> 外文期刊>Clinical immunology: The official journal of the Clinical Immunology Society >Activation of the human RANTES gene promoter in a macrophage cell line by lipopolysaccharide is dependent on stress-activated protein kinases and the IkappaB kinase cascade: implications for exacerbation of allergic inflammation by environmental poll
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Activation of the human RANTES gene promoter in a macrophage cell line by lipopolysaccharide is dependent on stress-activated protein kinases and the IkappaB kinase cascade: implications for exacerbation of allergic inflammation by environmental poll

机译:脂多糖对巨噬细胞系中人RANTES基因启动子的激活取决于应激激活的蛋白激酶和IkappaB激酶级联反应:环境调查加剧过敏性炎症的影响

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摘要

Macrophages are targeted by environmental pollutants and play a role in allergic inflammation. We explored the molecular basis for induction of RANTES (regulated upon activation, normal T-cells expressed and secreted) mRNA by lipopolysaccharide (LPS) and the redox-active quinone, tert-butylhydroxyquinone (tBHQ). We demonstrate that transcriptional activation of the human RANTES promoter by LPS is dependent on specific AP-1 and NF-kappaB response elements, which are regulated by c-Jun N-terminal kinase (JNK) and NF-kappaB kinase cascades, respectively. The transcriptional activation of the TRE3/4 site is mediated through the transcriptional activation of c-Jun by JNK. A c-Jun mutant which lacks a transcriptional activation domain interfered in the activation of the RANTES promoter. Similarly, kinase-inactive NF-kappaB inducing kinase interfered in the activation of the RANTES promoter. While activation of the RANTES promoter could also be blocked by the downstream kinase-inactive IkappaB kinases, only IKKalpha appears to be LPS-inducible. tBHQ also exerted subtle effects on the human RANTES promoter and induced mRNA expression in parallel with generating NF-kappaB shift complexes. Copyright 1999 Academic Press.
机译:巨噬细胞受到环境污染物的攻击,并在过敏性炎症中发挥作用。我们探索了通过脂多糖(LPS)和氧化还原活性醌,叔丁基羟基醌(tBHQ)诱导RANTES(受激活,正常T细胞表达和分泌的调节)mRNA诱导的分子基础。我们证明LPS的人RANTES启动子的转录激活取决于特定的AP-1和NF-kappaB反应元件,分别由c-Jun N末端激酶(JNK)和NF-kappaB激酶级联调节。 TRE3 / 4位点的转录激活是通过JNK对c-Jun的转录激活介导的。缺少转录激活域的c-Jun突变体会干扰RANTES启动子的激活。同样,激酶失活的NF-κB诱导激酶会干扰RANTES启动子的激活。虽然RANTES启动子的激活也可以被下游激酶失活的IkappaB激酶阻断,但只有IKKalpha似乎是LPS诱导的。 tBHQ还对人类RANTES启动子产生微妙的影响,并与生成NF-κB移位复合物同时诱导mRNA表达。版权所有1999,学术出版社。

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