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Expression and regulation of proton-coupled oligopeptide transporters in colonic tissue and immune cells of mice

机译:小鼠结肠组织和免疫细胞中质子偶联寡肽转运蛋白的表达和调节

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摘要

A number of studies have implicated proton-coupled oligopeptide transporters (POTs) in the initiation and/or progression of inflammatory bowel disease and immune cell signaling. With this in mind, the aim of this study was to delineate the expression of POTs in mouse colonic tissues and immune cells, and characterize the potential role of these transporters in nucleotide-binding oligomerization domain (NOD) signaling. Using a dextran sodium sulfate (DSS)-induced colitis mouse model, we found that DSS down regulated Phtl gene expression and up regulated Pht2 gene expression in colonic tissue and immune cells. In contrast, PEPT1 protein was absent from the colonic tissue and immune cells of normal and DSS-treated mice. NOD ligands, muramyl dipeptide (MDP) and L-Ala-gamma-D-Glu-meso-diaminopimelic acid (tri-DAP), were shown to be substrates of PHT2 in MDCK-hPHT2(19,20AA) cells. Subsequent studies revealed that the immune response of lamina propia mononuclear cells may be regulated by PHT1 and PHT2, and that PHT2 facilitated the NOD-dependent immune response in RAW264.7 macrophages. These results clarified the expression of POTs in mouse colonic segments, cells and subtypes, and the role of increased Pht2 expression during chemically-induced colitis in facilitating NOD-dependent immune response. The findings further suggest that intestinal PHT2 may serve as a therapeutic target for IBD therapy. (C) 2018 Elsevier Inc. All rights reserved.
机译:许多研究使质子偶联的寡肽转运蛋白(盆)掺杂在炎症性肠疾病和免疫细胞信号传导的起始和/或进展中。考虑到这项研究,本研究的目的是描绘小鼠结肠组织和免疫细胞中的盆的表达,并表征这些转运蛋白在核苷酸结合寡聚化结构域(NOD)信号传导中的潜在作用。使用葡聚糖硫酸钠(DSS) - 诱导的结肠炎小鼠模型,发现DSS下调ChTL基因表达及抑制结肠组织和免疫细胞的调节pHT2基因表达。相反,来自正常和DSS处理的小鼠的结肠组织和免疫细胞不存在Pept1蛋白。 NOD配体,蛋白二肽(MDP)和L-ALA-Gamma-D-Glu-Meso-二氨基丙酸(三-DAP)被显示为MDCK-HPHT2(19,20AA)细胞中pHT2的基材。随后的研究表明,薄层预核细胞的免疫应答可以通过PHT1和PHT2调节,并且PHT2促进Raw264.7巨噬细胞中的Nod依赖性免疫应答。这些结果阐明了小鼠结肠链段,细胞和亚型中的盆的表达,以及在化学诱导的结肠炎期间增加了PHT2表达的作用,促进了NOD依赖性免疫应答。结果进一步表明肠PHT2可以用作IBD治疗的治疗靶标。 (c)2018年Elsevier Inc.保留所有权利。

著录项

  • 来源
    《Biochemical Pharmacology》 |2018年第2018期|共11页
  • 作者单位

    Univ Michigan Coll Pharm Dept Pharmaceut Sci 428 Church St Ann Arbor MI 48109 USA;

    Univ Michigan Coll Pharm Dept Pharmaceut Sci 428 Church St Ann Arbor MI 48109 USA;

    Zhejiang Univ Lab Pharmaceut Anal &

    Drug Metab Zhejiang Prov Key Lab Anticanc Drug Res Coll;

    Zhejiang Univ Lab Pharmaceut Anal &

    Drug Metab Zhejiang Prov Key Lab Anticanc Drug Res Coll;

    Univ Michigan Sch Med Dept Internal Med Ann Arbor MI 48109 USA;

    Zhejiang Univ Lab Pharmaceut Anal &

    Drug Metab Zhejiang Prov Key Lab Anticanc Drug Res Coll;

    Univ Michigan Coll Pharm Dept Pharmaceut Sci 428 Church St Ann Arbor MI 48109 USA;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药理学;
  • 关键词

    Colon; Immune cells; Proton-coupled oligopeptide transporters; NOD1/2; Immune response;

    机译:结肠;免疫细胞;质子偶联的寡肽转运蛋白;NOD1 / 2;免疫应答;
  • 入库时间 2022-08-19 22:54:19

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