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首页> 外文期刊>Journal of Lipid Research >25-Hydroxycholesterol activates the expression of cholesterol 25-hydroxylase in an LXR-dependent mechanism
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25-Hydroxycholesterol activates the expression of cholesterol 25-hydroxylase in an LXR-dependent mechanism

机译:25-羟基胆固醇在LXR依赖性机制中激活胆固醇25-羟化酶的表达

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摘要

Cholesterol 25-hydroxylase (CH25H) catalyzes the production of 25-hydroxycholesterol (25-HC), an oxysterol that can play an important role in different biological processes. However, the mechanisms regulating CH25H expression have not been fully elucidated. In this study, we determined that CH25H is highly expressed in mouse liver and peritoneal macrophages. We identified several liver X receptor (LXR) response elements (LXREs) in the human CH25H promoter. In HepG2 cells, activation of LXR by 25-HC or other oxysterols and synthetic ligands [T0901317 (T317) and GW3965] induced CH25H protein expression, which was associated with increased CH25H mRNA expression. 25-HC or T317 activated CH25H transcription in an LXRE-dependent manner. Thus, high-expressing LXR alpha or LXR beta activated CH25H expression, and the activation was further enhanced by LXR ligands. In contrast, inhibition of LXR alpha/beta expression attenuated 25-HC or T317-induced CH25H expression. Deficiency of interferon gamma expression reduced, but did not block, LXR ligand-induced hepatic CH25H expression. Activation of LXR also substantially induced macrophage CH25H expression. In vivo, administration of GW3965 to mice increased CH25H expression in both liver and peritoneal macrophages. Taken together, our study demonstrates that 25-HC can activate CH25H expression in an LXR-dependent manner, which may be an important mechanism to exert the biological actions of 25-HC.
机译:胆固醇25-羟化酶(CH25H)催化生产25-羟基胆固醇(25-HC),氧毒剂可以在不同的生物过程中发挥重要作用。然而,调节CH25H表达的机制尚未完全阐明。在这项研究中,我们确定CH25H在小鼠肝脏和腹膜巨噬细胞中高度表达。我们在人CH25H启动子中鉴定了几种肝X受体(LXR)反应元素(LXRES)。在HepG2细胞中,通过25-HC或其他氧胆酚和合成配体的LXR激活[T0901317(T317)和GW3965]诱导的CH25H蛋白表达,其与增加的CH25H mRNA表达相关。以依赖依赖性方式,25-HC或T317活化CH25H转录。因此,通过LXR配体进一步增强了高表达的LXRα或LXRβ活化的CH25H表达,并进一步增强了活化。相反,抑制LXRα/β表达衰减25-HC或T317诱导的CH25H表达。干扰素γ表达的缺乏减少,但没有阻断LXR配体诱导的肝CH25H表达。 LXR的激活还大致诱导了巨噬细胞CH25H表达。体内,给予肝脏和腹膜巨噬细胞的小鼠GW3965给小鼠增加CH25H表达。我们的研究表明,25-HC可以以LXR依赖性方式激活CH25H表达,这可能是施加25-HC的生物学作用的重要机制。

著录项

  • 来源
    《Journal of Lipid Research 》 |2018年第3期| 共13页
  • 作者单位

    Nankai Univ Coll Life Sci Dept Biochem &

    Mol Biol Tianjin Peoples R China;

    Nankai Univ Coll Life Sci Dept Biochem &

    Mol Biol Tianjin Peoples R China;

    Cleveland Clin Lerner Res Inst Dept Immunol Cleveland OH 44106 USA;

    Hefei Univ Technol Coll Biomed Engn Dept Biomed Sci Hefei Anhui Peoples R China;

    Nankai Univ Coll Life Sci Dept Biochem &

    Mol Biol Tianjin Peoples R China;

    Nankai Univ Coll Life Sci Dept Biochem &

    Mol Biol Tianjin Peoples R China;

    Nankai Univ Coll Life Sci Dept Biochem &

    Mol Biol Tianjin Peoples R China;

    Med Coll Wisconsin Dept Surg Milwaukee WI 53226 USA;

    Cornell Univ Weill Cornell Med Coll Dept Pathol New York NY 10021 USA;

    Hefei Univ Technol Coll Biomed Engn Dept Biomed Sci Hefei Anhui Peoples R China;

    Hefei Univ Technol Coll Biomed Engn Dept Biomed Sci Hefei Anhui Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学 ;
  • 关键词

    hepatocytes; 25-hydroxycholesterol; interferon-gamma; liver X receptor;

    机译:肝细胞;25-羟基胆固醇;干扰素-γ;肝X受体;

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