首页> 外文期刊>Journal of orthopaedic research >Macrophage‐derived inflammatory cytokines regulate growth factors and pain‐related molecules in mice with intervertebral disc injury
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Macrophage‐derived inflammatory cytokines regulate growth factors and pain‐related molecules in mice with intervertebral disc injury

机译:巨噬细胞源性炎症细胞因子调节小鼠中的生长因子和疼痛相关分子,椎间盘损伤

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摘要

ABSTRACT Upregulation of inflammatory cytokines and various growth factors is a significant contributor to discogenic low back pain. The aim of this study was to investigate possible regulation of pain‐related molecules by macrophages and the role of macrophage‐derived molecules in injured intervertebral disc (IVD)s. C57BL/6J mice were used in this study. We characterized the expression profiles of genes for tumor necrosis factor (TNF)‐alpha, interleukin (IL)‐1beta, nerve growth factor (NGF), and vascular endothelial growth factor (VEGF) in both intact and injured IVDs. We examined whether macrophage depletion, induced by systemic injection of clodronate‐laden liposomes, affected the expression of these molecules in injured IVDs. The effect of TNF‐alpha on cultured F4/80‐CD11b‐cells in injured IVDs was investigated. Expression of TNF‐alpha and IL‐1beta was significantly increased in injured IVDs, but decreased by macrophage depletion. Expression of NGF and VEGF was also significantly increased, but by contrast was not decreased by macrophage depletion. TNF‐alpha treatment of F4/80‐cells from injured IVDs upregulated NGF, VEGF, cyclooxygenase (COX)‐2, and microsomal prostaglandin E synthase‐1 (mPGES1). IVD injury upregulated inflammatory cytokines and various growth factors. Macrophages in the injured IVDs produced inflammatory cytokines, but not growth factors. Macrophage‐derived inflammatory cytokines regulate growth factors and pain‐related molecules. These findings demonstrate further complexity in the pathogenesis of discogenic pain. ? 2018 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 36:2274–2279, 2018.
机译:摘要炎症细胞因子的上调和各种生长因子是一种致病腰痛的重要因素。本研究的目的是通过巨噬细胞调查疼痛相关分子的可能调节,以及巨噬细胞衍生分子在受伤的椎间盘(IVD)S中的作用。在本研究中使用了C57BL / 6J小鼠。我们在完整和受伤的IVDS中表征了肿瘤坏死因子(TNF),白细胞介素(IL)-1beta,神经介素(IL)-1beta,神经生长因子(NGF)和血管内皮生长因子(VEGF)的表达谱。我们检查了通过全身注射氯氰酸盐脂质脂质体引起的巨噬细胞耗尽是否影响了这些分子在受伤的IVD中的表达。研究了TNF-α对受伤IVDS中培养的F4 / 80-CD11B细胞的影响。受损IVDS的表达明显增加,但通过巨噬细胞耗尽降低。 NGF和VEGF的表达也显着增加,但通过巨噬细胞耗尽不会降低。 TNF-α从受损IVDS上调NGF,VEGF,环氧化酶(COX)-2和微粒体前列腺素E合酶-1(MPGES1)的TNF-α处理F4 / 80细胞。 IVD损伤上调炎症细胞因子和各种生长因子。受伤的IVDS中的巨噬细胞产生炎症细胞因子,但不是生长因素。巨噬细胞衍生的炎症细胞因子调节生长因子和疼痛相关分子。这些研究结果表明了致畸疼痛的发病机制的进一步复杂性。还2018骨科研究会。由Wiley Hearygers,Inc.J orthop Res 36:2274-2279,2018。

著录项

  • 来源
    《Journal of orthopaedic research》 |2018年第8期|共6页
  • 作者单位

    Department of Orthopedic SurgeryKitasato University School of Medicine1‐15‐1 Minami‐ku Kitasato;

    Department of Orthopedic SurgeryKitasato University School of Medicine1‐15‐1 Minami‐ku Kitasato;

    Department of Orthopedic SurgeryKitasato University School of Medicine1‐15‐1 Minami‐ku Kitasato;

    Department of Orthopedic SurgeryKitasato University School of Medicine1‐15‐1 Minami‐ku Kitasato;

    Department of Orthopedic SurgeryKitasato University School of Medicine1‐15‐1 Minami‐ku Kitasato;

    Department of Orthopedic SurgeryKitasato University School of Medicine1‐15‐1 Minami‐ku Kitasato;

    Department of Orthopedic SurgeryKitasato University School of Medicine1‐15‐1 Minami‐ku Kitasato;

    Department of Orthopaedic SurgeryChiba University1‐8‐1 Inohana Chuo‐ku Chiba 260‐8670 Japan;

    Department of Orthopedic SurgeryKitasato University School of Medicine1‐15‐1 Minami‐ku Kitasato;

    Department of Orthopedic SurgeryKitasato University School of Medicine1‐15‐1 Minami‐ku Kitasato;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 骨科学(运动系疾病、矫形外科学);
  • 关键词

    disc biology; spine;

    机译:圆盘生物学;脊柱;

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