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慢性变应原刺激诱导 BALB/c 而非 C57BL/6 小鼠支气管肥大细胞积聚,且不依赖于白细胞介素-9。

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

机构信息

Department of Medicine, University of California San Diego, San Diego, CA, USA.

出版信息

Immunogenetics. 2010 Aug;62(8):499-506. doi: 10.1007/s00251-010-0452-1. Epub 2010 May 18.

DOI:10.1007/s00251-010-0452-1
PMID:20480160
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2910299/
Abstract

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 microm), medium (90-155 microm), or large (>150 microm) 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.

摘要

由于通常在 C57BL/6 背景下生成缺乏单个基因的基因工程突变小鼠,因此为了研究肥大细胞在突变小鼠中的迁移,我们最初研究了 C57BL/6 小鼠在急性或慢性 1 至 3 个月内用 OVA 变应原挑战时,支气管中是否积累了肥大细胞。使用甲苯胺蓝染色法对不同大小的气道中的支气管肥大细胞总数进行定量,即小气道(<90 微米)、中气道(90-155 微米)或大气道(>150 微米)。未接受 OVA 挑战和急性 OVA 挑战的 C57BL/6 和 BALB/c 小鼠没有检测到支气管肥大细胞。慢性 OVA 挑战 BALB/c 小鼠 1 或 3 个月可显著增加小、中、大气道中支气管肥大细胞的数量,但 C57BL/6 小鼠中支气管肥大细胞的数量变化很小。急性或慢性 OVA 挑战后,BALB/c 和 C57BL/6 小鼠均发生明显的肺嗜酸性粒细胞增多。在 BALB/c 背景下研究 IL-9 缺陷型小鼠表明,IL-9 缺陷型小鼠中支气管肥大细胞的数量显著增加,表明 IL-9 不是支气管肥大细胞积聚所必需的。总的来说,这些研究表明,我们在 BALB/c 小鼠中使用的慢性 OVA 挑战方案为研究支气管肥大细胞积聚的机制提供了模型,并且在该模型中,慢性 OVA 挑战小鼠中支气管肥大细胞的积聚不依赖于 IL-9。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a223/2910299/229c7e3aa1bd/251_2010_452_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a223/2910299/42ed08820cf4/251_2010_452_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a223/2910299/8d6f08b822b6/251_2010_452_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a223/2910299/4b938316586d/251_2010_452_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a223/2910299/229c7e3aa1bd/251_2010_452_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a223/2910299/42ed08820cf4/251_2010_452_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a223/2910299/8d6f08b822b6/251_2010_452_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a223/2910299/4b938316586d/251_2010_452_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a223/2910299/229c7e3aa1bd/251_2010_452_Fig4_HTML.jpg

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2
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Immunity. 2009 Sep 18;31(3):425-37. doi: 10.1016/j.immuni.2009.08.014.
3
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World Allergy Organ J. 2019 Apr 20;12(4):100028. doi: 10.1016/j.waojou.2019.100028. eCollection 2019.
4
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5
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