MicroRNA-21 Inhibition Suppresses Alveolar M2 Macrophages in an Ovalbumin-Induced Allergic Asthma Mice Model

被引:34
作者
Lee, Hwa Young [1 ]
Hur, Jung [1 ]
Kang, Ji Young [1 ]
Rhee, Chin Kook [1 ]
Lee, Sook Young [1 ]
机构
[1] Catholic Univ Korea, Coll Med, Seoul St Marys Hosp, Dept Internal Med,Div Allergy Pulm & Crit Care Me, 222 Banpo Daero, Seoul 06591, South Korea
基金
新加坡国家研究基金会;
关键词
Asthma; microRNAs; macrophages; miR-21; antagomir; AHR; MURINE MODEL; MOUSE MODEL; POLARIZATION; INFLAMMATION; ACTIVATION; DYSFUNCTION; CHALLENGE; MONOCYTES;
D O I
10.4168/aair.2021.13.2.312
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Purpose: MicroRNA-21 (miR-21) influences the Th2 immune pathway by suppressing the expressions of interleukin (IL)-12 and interferon (IFN)-gamma. The effects of miR-21 suppression on alveolar macrophage polarization and airway inflammation are not known. Methods: BALB/c and miR-21 knockout (KO) mice were sensitized and challenged with ovalbumin (OVA). The anti-miR-21 antagomir was administered to BALB/c mice by intranasal inhalation from the day of OVA sensitization. Changes in cell counts, cytokine levels in bronchoalveolar lavage fluid (BALF), and airway hyperresponsiveness (AHR) were examined. Total, M1, and M2 macrophages were examined in the lung tissues by immunohistochemistry (IHC). M2 macrophages from the OVA mice lung were inhaled into the anti-miR-21 antagomir-treated asthmatic mice. Moreover, the polarization of M0 to M2 macrophages upon IL-4 stimulation was analyzed after anti-miR-21 antagomir transfection. Results: The miR-21 KO mice showed decreases in AHR, total cell and eosinophil counts in BALF, and in the levels of IL-4, IL-5, IL-10, and IL-13. Expression of IL-12 and IFN-gamma were increased in the miR-21 KO mice. Peribronchial inflammation and goblet cell dysplasia were significantly decreased in the lung tissues of miR-21 KO OVA mice compared to the wild type OVA mice. IHC for Ml, M2, and total macrophage in the lung tissues showed that miR-21 inhalation suppressed alveolar M2 macrophages in KO mice. M2 macrophage inhalation restored AHR and eosinophilic airway inflammation in the miR-21 antagomir-treated mice. Moreover, anti-miR-21 antagomir transfection decreased the expression of M2 markers and increased the expression of M1 markers in M0 macrophages after IL-4 stimulation. Conclusions: The results suggest that miR-21 antagonism could suppress alveolar M2 macrophage polarization, decreasing not only the Th2 eosinophilic airway inflammation but also AHR and airway remodeling process.
引用
收藏
页码:312 / 329
页数:18
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