...
首页> 外文期刊>The international journal of biochemistry and cell biology >Changes of hepatic lactoferrin gene expression in two mouse models of the acute phase reaction.
【24h】

Changes of hepatic lactoferrin gene expression in two mouse models of the acute phase reaction.

机译:两种小鼠急性期反应模型中肝乳铁蛋白基因表达的变化。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Lactoferrin (Ltf), an iron binding glycoprotein, is a pleiotropic molecule whose serum concentration increases under acute phase conditions. The physiological roles of this protein have been well elucidated, but the source and serum regulation of Ltf gene expression have not been investigated in detail as part of the acute phase reaction (APR). In the current work, the changes in hepatic Ltf-gene-expression during turpentine oil- (TO-) or LPS-induced APR were investigated. Ltf was upregulated at both the mRNA and protein levels in the liver of TO- and LPS-treated wild type (WT) mice. The pattern of induction however was different in both animal models indicating distinctive signalling patterns resulting in an acute phase reaction. Cytokines are the core regulators of APR. Among the major cytokines, IL-6 is an important signalling molecule, which also regulates iron homeostasis in response to an inflammatory situation. In this study, the administration of IL-6 induced Ltf gene expression in the liver of WT mice, in murine hepatocytes and in hepa 1-6 cells. Ltf-gene-expression was upregulated also in the liver of TO- and LPS-treated IL-6 knockout (KO) mice. The increase in serum Ltf after LPS injection was greater than after TO-injection both in WT and IL-6-KO mice. To evaluate the contribution of other acute phase cytokines in the regulation of Ltf-gene-expression in the liver, both in vitro and in vivo studies with IL-1beta, TNF-alpha, or IFN-gamma were performed. The results demonstrate that TNF-alpha and IFN-gamma also upregulated Ltf-gene-expression, while IL-1beta has no role in the regulation of Ltf-gene-expression.
机译:乳铁蛋白(Ltf)是一种铁结合糖蛋白,是一种多效性分子,在急性期条件下其血清浓度会增加。这种蛋白质的生理作用已得到很好的阐明,但是作为急性期反应(APR)的一部分,尚未详细研究Ltf基因表达的来源和血清调节。在当前的工作中,研究了松节油(TO-)或LPS诱导的APR期间肝Ltf基因表达的变化。在接受TO和LPS处理的野生型(WT)小鼠肝脏中,Ltf在mRNA和蛋白水平上均上调。然而,两种动物模型的诱导模式不同,表明独特的信号传导模式导致了急性期反应。细胞因子是APR的核心调节因子。在主要的细胞因子中,IL-6是重要的信号分子,它也可响应炎症情况调节铁稳态。在这项研究中,IL-6的施用在野生型小鼠肝脏,鼠肝细胞和肝1-6细胞中诱导了Ltf基因表达。在接受TO和LPS治疗的IL-6基因敲除(KO)小鼠的肝脏中,Ltf基因的表达也被上调。在WT和IL-6-KO小鼠中,LPS注射后血清Ltf的增加大于TO注射后。为了评估其他急性期细胞因子在调节肝脏Ltf基因表达中的作用,进行了使用IL-1beta,TNF-α或IFN-γ的体外和体内研究。结果表明,TNF-α和IFN-γ也上调了Ltf基因的表达,而IL-1beta在调节Ltf基因的表达中没有作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号