miR-146a regulates emphysema formation and abnormal inflammation in the lungs of two mouse models

miR-146a, a microRNA (miRNA) that regulates inflammatory responses, plays an important role in many inflammatory diseases. Although an in vitro study had suggested that miR-146a is involved in abnormal inflammatory response, being a critical factor in the pathogenesis of chronic obstructive pulmonar...

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Veröffentlicht in:American journal of physiology. Lung cellular and molecular physiology 2024-01, Vol.326 (1), p.L98-L110
Hauptverfasser: Yoshikawa, Hitomi, Sato, Tadashi, Horikoshi, Kimiko, Komura, Moegi, Nitta, Naoko Arano, Mitsui, Aki, Koike, Kengo, Kodama, Yuzo, Takahashi, Kazuhisa
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Sprache:eng
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Zusammenfassung:miR-146a, a microRNA (miRNA) that regulates inflammatory responses, plays an important role in many inflammatory diseases. Although an in vitro study had suggested that miR-146a is involved in abnormal inflammatory response, being a critical factor in the pathogenesis of chronic obstructive pulmonary disease (COPD), in vivo evidence of its pathogenic role in COPD remains limited. Eight-week-old male B6(FVB)-Mir146tm1.1Bal/J [miR-146a knockout (KO)] and C57BL/6J mice were intratracheally administered elastase and evaluated after 28 days or exposed to cigarette smoke (CS) and evaluated after 5 mo. miR-146a expression was significantly increased in C57BL/6J mouse lungs due to elastase administration ( = 0.027) or CS exposure ( = 0.019) compared with that in the control group. Compared with C57BL/6J mice, elastase-administered miR-146a-KO mice had lower average computed tomography (CT) values ( = 0.017) and increased lung volume-to-weight ratio ( = 0.016), mean linear intercept ( < 0.001), and destructive index ( < 0.001). Moreover, total cell ( = 0.006), macrophage ( = 0.001), neutrophil ( = 0.026), chemokine (C-X-C motif) ligand 2/macrophage inflammatory protein-2 [ = 0.045; in bronchoalveolar lavage fluid (BALF)], , and levels were all increased (in the lungs). Following long-term CS exposure, miR-146a-KO mice showed a greater degree of emphysema formation in their lungs and inflammatory response in the BALF and lungs than C57BL/6J mice. Collectively, miR-146a protected against emphysema formation and the associated abnormal inflammatory response in two murine models. This study demonstrates that miR-146a expression is upregulated in mouse lungs because of elastase- and CS-induced emphysema and that the inflammatory response by elastase or CS is enhanced in the lungs of miR-146a-KO mice than in those of control mice, resulting in the promotion of emphysema. This is the first study to evaluate the protective role of miR-146a in emphysema formation and the associated abnormal inflammatory response in different in vivo models.
ISSN:1040-0605
1522-1504
DOI:10.1152/ajplung.00080.2023