Abstract | PURPOSE: METHODS: MIF knockdown in the lung tissues of C57BL/6 mice was conducted by instilling intratracheally adeno-associated virus (AAV) vectors (MIF-mutant AAV9) into mouse lung tissues. Mice genetically deficient in the autophagy marker ATG5 (ATG5+/-) was used to detect the role of autophagy in ovalbumin (OVA)-asthmatic murine models. Moreover, to block the expression of MIF and CD74 in vitro models, inhibitors, antibodies and lentivirus transfection techniques were employed. RESULTS: First, MIF knockdown in the lung tissues of mice showed markedly reduced airway remodeling in OVA murine mice models. Secondly, ASMC autophagy was increased in the OVA-challenged models. Mice genetically deficient in the autophagy marker ATG5 (ATG5+/-) that were primed and challenged with OVA showed lower airway remodeling than genetically wild-type asthmatic mice. Thirdly, MIF can induce ASMC autophagy in vitro. Moreover, the cellular source of MIF which promoted ASMC autophagy was macrophages. Finally, MIF promoted ASMC autophagy in a CD74-dependent manner. CONCLUSIONS: MIF can increase asthmatic airway remodeling by enhancing ASMC autophagy. Macrophage-derived MIF can promote ASMC autophagy by targeting CD74.
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Authors | Ruyi Li, Feiyun Wang, Jianghong Wei, Yun Lin, Guofang Tang, Lizong Rao, Libing Ma, Qing Xu, Jingjie Wu, Qian Lv, Rui Zhou, Huiren Lei, Xueqiang Zhao, Dong Yao, Bo Xiao, Haiming Huang, Jiange Zhang, Biwen Mo |
Journal | Allergy, asthma & immunology research
(Allergy Asthma Immunol Res)
Vol. 13
Issue 1
Pg. 88-105
(Jan 2021)
ISSN: 2092-7355 [Print] Korea (South) |
PMID | 33191679
(Publication Type: Journal Article)
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Copyright | Copyright © 2021 The Korean Academy of Asthma, Allergy and Clinical Immunology · The Korean Academy of Pediatric Allergy and Respiratory Disease. |