Interleukin-18 has an Important Role in Differentiation and Maturation of Mucosal Mast Cells.

Journal of mucosal immunology research Pub Date : 2018-01-01 Epub Date: 2018-07-02
Nathan L Sandersa, Sathisha Upparahalli Venkateshaiah, Murli Manohar, Alok K Verma, Hemanth K Kandikattu, Anil Mishra
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Abstract

A significant amount of correlational evidence has linked increased levels of IL-18 with allergic diseases in both human and animal models, and, as mast cells are major mediators of allergies, we hypothesized that IL-18 may have a role in mast cell biology. Rationale for our hypothesis is based on the evidence that IL-3 deficient mice are not devoid of mast cells, even though IL-3 is a major differentiation and growth factor for mast cells. Accordingly, we cultured IL-18 responsive bone marrow CD34+ cells in vitro under a variety of conditions and cytokine combinations to examine mast cell differentiation and maturation using flow cytometry, quantitative PCR,and immunostaining techniques. Additionally, in vivo mast cell transformation and maturation were also analysed using endogenous IL-18 gene-deficient or Fabpi-IL-18 overexpressed mice. Our data indicate that both IL-3 and IL-18 exposed CD34+ bone marrow precursors differentiate and mature into mast cells. Further, we observed that IL-18 differentiates mast cells independent of IL-3, as pharmacologic blockade of IL-3 does not prevent in vitro IL-18-driven mast cell differentiation. Further, we found that endogenous IL-18 deficiency restricts maturation of IL-3 generated mast cells and IL-18 derived mast cells require IL-3 for their survival. Additionally, we observed IL-18 intestinal overexpression promotes tissue mast cell proliferation and mucosal mast cell development. Taken together, we provide the evidence that IL-18 has an important contributory role in mast cell differentiation, maturation and in vivo development of mucosal mast cells. Therefore, IL-18 may represent a future pharmacologic target for treating mast cell-mediated allergic diseases.

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白细胞介素-18在粘膜肥大细胞的分化和成熟过程中起重要作用。
大量相关证据表明,人类和动物模型中IL-18水平升高与过敏性疾病有关,并且,由于肥大细胞是过敏的主要介质,我们假设IL-18可能在肥大细胞生物学中起作用。我们假设的基本原理是基于IL-3缺陷小鼠并非缺乏肥大细胞的证据,尽管IL-3是肥大细胞的主要分化和生长因子。因此,我们在多种条件和细胞因子组合下体外培养IL-18应答骨髓CD34+细胞,使用流式细胞术、定量PCR和免疫染色技术检测肥大细胞的分化和成熟。此外,还使用内源性IL-18基因缺陷或Fabpi-IL-18过表达的小鼠分析了体内肥大细胞的转化和成熟。我们的数据表明IL-3和IL-18暴露于CD34+骨髓前体细胞分化并成熟为肥大细胞。此外,我们观察到IL-18独立于IL-3分化肥大细胞,因为IL-3的药物阻断不会阻止IL-18驱动的体外肥大细胞分化。此外,我们发现内源性IL-18缺乏限制了IL-3生成的肥大细胞的成熟,而IL-18衍生的肥大细胞需要IL-3才能存活。此外,我们观察到IL-18肠道过表达促进组织肥大细胞增殖和粘膜肥大细胞发育。综上所述,我们提供的证据表明IL-18在肥大细胞分化、成熟和粘膜肥大细胞的体内发育中起着重要的促进作用。因此,IL-18可能是治疗肥大细胞介导的过敏性疾病的未来药理学靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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