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Chronic allergen challenge induces bronchial mast cell accumulation in BALB/c but not C57BL/6 mice and is independent of IL-9

机译:慢性过敏原激发可诱导BALB / c小鼠支气管肥大细胞蓄积但不引起C57BL / 6小鼠蓄积且独立于IL-9

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摘要

As genetically engineered mutant mice deficient in single genes are usually generated on a C57BL/6 background, to study mast cell trafficking in mutant mice, we initially investigated whether mast cells accumulated in bronchi in C57BL/6 mice challenged with OVA allergen acutely or chronically for 1 to 3 months. The total number of bronchial mast cells were quantitated using toluidine blue staining in airways of different sizes, i.e. , small (<90 µm), medium (90–155 µm), or large (>150 µm) airways. Non-OVA challenged and acute OVA challenged mice (C57BL/6 and BALB/c) had no detectable bronchial mast cells. Chronic OVA challenge in BALB/c mice for 1 or 3 months induced a significant increase in the number of bronchial mast cells in small-, medium-, and large-sized airways but minimal change in the number of bronchial mast cells in C57BL/6 mice. Both BALB/c and C57BL/6 mice developed significant lung eosinophilia following acute or chronic OVA challenge. Studies of IL-9-deficient mice on a BALB/c background demonstrated a significant increase in the number of bronchial mast cells in IL-9-deficient mice suggesting that IL-9 was not required for the bronchial accumulation of mast cells. Overall, these studies demonstrate that the chronic OVA challenge protocol we have utilized in BALB/c mice provides a model to study the mechanism of bronchial mast cell accumulation and that bronchial mast cell accumulation in chronic OVA challenged mice is independent of IL-9 in this model.
机译:由于通常在C57BL / 6背景上产生缺乏单个基因的基因工程突变小鼠,为了研究突变小鼠中的肥大细胞贩运,我们最初调查了急性或慢性OVA过敏原攻击的C57BL / 6小鼠支气管中是否积聚了肥大细胞。 1至3个月。在不同大小的气道中使用甲苯胺蓝染色对支气管肥大细胞的总数进行定量,即小(<90 µm),中(90-155 µm)或大(> 150 µm)气道。非OVA攻击和急性OVA攻击的小鼠(C57BL / 6和BALB / c)没有可检测的支气管肥大细胞。 BALB / c小鼠进行1或3个月的慢性OVA攻击后,小,中和大型气道的支气管肥大细胞数量显着增加,但C57BL / 6的支气管肥大细胞数量变化很小老鼠。在急性或慢性OVA攻击后,BALB / c和C57BL / 6小鼠均出现明显的肺嗜酸性粒细胞增多。在BALB / c背景上对IL-9缺陷型小鼠的研究表明,IL-9缺陷型小鼠中支气管肥大细胞的数量显着增加,这表明肥大细胞的支气管积聚不需要IL-9。总体而言,这些研究表明我们在BALB / c小鼠中使用的慢性OVA攻击方案为研究支气管肥大细胞积累的机制提供了模型,并且在这种情况下,在慢性OVA攻击小鼠中支气管肥大细胞的积累独立于IL-9模型。

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