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 |
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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. |
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ISSN: | 1040-0605 1522-1504 |
DOI: | 10.1152/ajplung.00080.2023 |