Targeting circNCLN/miR-291a-3p/TSLP signaling axis alleviates lipopolysaccharide-induced acute lung injury

被引:9
|
作者
Cao, Jianwei [1 ]
Kuang, Daibin [2 ]
Luo, Ming [2 ]
Wang, Shanzhong [2 ]
Fu, Chunlai [1 ,2 ,3 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Resp & Crit Care Med, Chron Airways Dis Lab, Guangzhou, Guangdong, Peoples R China
[2] Southern Med Univ, Affiliated Dongguan Hosp, Dongguan Peoples Hosp, Dept Emergency Intens Care Unit, Dongguan, Guangdong, Peoples R China
[3] 78 Wandao Rd,Wanjiang St, Dongguan 523058, Guangdong, Peoples R China
关键词
Acute lung injury; LPS; TSLP; circRNA; microRNA; ASO;
D O I
10.1016/j.bbrc.2022.05.095
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Acute lung injury (ALI) is a life-threatening disease caused by the severe and acute response of the lungs to a variety of direct and indirect insults. Patients with ALI are currently treated mainly with respiratory support due to inadequate understanding of ALI progression. Alveolar epithelial cells produced thymic stromal lymphopoietin (TSLP) has been proved to worsen ALI by triggering airway inflammation. However, the regulation mechanism of TSLP expression remains unclear. In this study, we identified the crucial role played by circNCLN in lipopolysaccharide (LPS)-induced ALI. We demonstrated for the first time that miR-291a-3p could directly bind to the 30UTR of TSLP and suppress TSLP expression in alveolar epithelial cells. Mechanistically, our data identified that circNCLN acts as a molecular sponge to antagonize miR-291a-3p and thereby maintaining the expression of TSLP in alveolar epithelial cells. Importantly, targeting circNCLN by its antisense oligonucleotide (ASO) markedly alleviated LPS-induced ALI. Therefore, our results suggested that circNCLN/miR-291a-3p/TSLP axis may be an important signaling in LPS-induced ALI and circNCLN inhibition may serve as a potential treatment of ALI. (C) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:60 / 67
页数:8
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