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Alveolar macrophages modulate allergic inflammation in a murine model of asthma

机译:肺泡巨噬细胞调节哮喘小鼠模型的过敏性炎症

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摘要

The role of alveolar macrophages (AMs) in the pathogenesis of asthma is still unknown. The aim of the present study was to investigate the effects of AM in the murine model of asthma. AMs were selectively depleted by liposomes containing clodronate just before allergen challenges, and changes in inflammatory cells and cytokine concentrations in bronchoalveolar lavage (BAL) fluid were measured. AMs were then adoptively transferred to AM-depleted sensitized mice and changes were measured. Phenotypic changes in AMs were evaluated after in vitro allergen stimulation. AM-depletion after sensitization significantly increased the number of eosinophils and lymphocytes and the concentrations of IL-4, IL-5 and GM-CSF in BAL fluid. These changes were significantly ameliorated only by adoptive transfer of unsensitized AMs, not by sensitized AMs. In addition, in vitro allergen stimulation of AMs resulted in their gaining the ability to produce inflammatory cytokines, such as IL-1β, IL-6 and TNF-α, and losing the ability to suppress GM-CSF concentrations in BAL fluid. These findings suggested that AMs worked probably through GM-CSF-dependent mechanisms, although further confirmatory experiments are needed. Our results indicate that the role of AMs in the context of airway inflammation should be re-examined.
机译:肺泡巨噬细胞(AMs)在哮喘发病机理中的作用仍然未知。本研究的目的是研究AM在哮喘小鼠模型中的作用。在过敏原激发之前,通过含氯膦酸盐的脂质体选择性清除AMs,并测量支气管肺泡灌洗液(BAL)中炎症细胞和细胞因子浓度的变化。然后将AMs过继转移到AM缺失的致敏小鼠中,并测量变化。体外变应原刺激后评估AMs的表型变化。致敏后AM耗竭显着增加BAL液中嗜酸性粒细胞和淋巴细胞的数量以及IL-4,IL-5和GM-CSF的浓度。仅通过未敏化AM的过继转移,而不是通过敏化AM,显着改善了这些变化。另外,AM的体外变应原刺激导致它们获得产生炎性细胞因子如IL-1β,IL-6和TNF-α的能力,而失去抑制BAL液中GM-CSF浓度的能力。这些发现表明,尽管可能需要进一步的验证性实验,但AM可能是通过依赖GM-CSF的机制起作用的。我们的结果表明,应重新检查AMs在气道炎症中的作用。

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