microRNA‐145‐5p attenuates acute lung injury via targeting ETS2

Autor: Liang Qiao, Rong‐Xia Li, Shan‐Gang Hu, Yu Liu, Hong‐Qiang Liu, Hong‐Jun Wu
Jazyk: angličtina
Rok vydání: 2022
Předmět:
Zdroj: Kaohsiung Journal of Medical Sciences, Vol 38, Iss 6, Pp 565-573 (2022)
Druh dokumentu: article
ISSN: 2410-8650
1607-551X
DOI: 10.1002/kjm2.12556
Popis: Abstract The protective effect of microRNA (miR)‐145‐5p in acute lung injury (ALI) has been discovered previously. Thus, in this study, we attempted to further investigate the mechanism of miR‐145‐5p in ALI through the downstream E26 transformation‐specific proto‐oncogene 2 (ETS2)/transforming growth factor β1 (TGF‐β1)/Smad pathway. A lipopolysaccharide (LPS)‐induced ALI rat model was established. The expression of miR‐145‐5p in ALI rat lung tissues was up‐regulated. Afterward, pathological damage in the lung tissue, the wet/dry (W/D) ratio, apoptosis, and serum inflammatory factor contents were observed. miR‐145‐5p, ETS2, TGF‐β1, Smad2/3, and phosphorylated Smad2/3 levels were measured in rats. miR‐145‐5p expression was down‐regulated, ETS2 expression was up‐regulated, and the TGF‐β1/Smad pathway was activated in LPS‐exposed rats. Overexpression of miR‐145‐5p inactivated the TGF‐β1/Smad pathway and attenuated ALI, as reflected by relieved pathological damage, a decreased W/D ratio, reduced apoptosis, and suppressed inflammatory response. In contrast, loss of miR‐145‐5p or elevated ETS2 levels worsened ALI and activated the TGF‐β1/Smad pathway. Moreover, elevation of ETS2 diminished miR‐145‐5p‐mediated protection against ALI. Evidently, miR‐145‐5p negatively regulates ETS2 expression and inactivates the TGF‐β1/Smad pathway to ameliorate ALI in rats.
Databáze: Directory of Open Access Journals
Externí odkaz: