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The circular RNA circTXNRD1 promoted ambient particulate matter-induced inflammation in human bronchial epithelial cells by regulating miR-892a/COX-2 axis.

Authors :
Wang, Jian
Zhu, Mengchan
Song, Juan
Zeng, Yingying
Xia, Shijin
Chen, Cuicui
Jin, Meiling
Song, Yuanlin
Source :
Chemosphere. Jan2022:Part 1, Vol. 286, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

Particulate matter (PM)-induced airway inflammation contributes to the development and exacerbation of chronic airway diseases. Circular RNA (circRNA) is a new class of non-coding RNA that participates in gene regulation in various respiratory diseases, but the regulatory role of circRNA in PM-induced airway inflammation has not been fully elucidated. In this study, we performed the human circRNA microarray to reveal differentially expressed circRNAs in PM-induced human bronchial epithelial cells (HBECs). A total of 176 upregulated and 15 downregulated circRNAs were identified. Of these, a new circRNA termed circTXNRD1 was upregulated by PM exposure in a dose- and time-dependent manner. Knockdown of circTXNRD1 significantly attenuated PM-induced expression of proinflammatory cytokine interleukin 6 (IL-6). CircRNA pull-down, dual-luciferase reporter assay and fluorescence in situ hybridization showed that circTXNRD1 acted as an endogenous sponge to decrease miR-892a levels in HBECs. Downregulation of miR-892a could increase cyclooxygenase-2 (COX-2) expression and eventually promote IL-6 secretion in PM-induced HBECs. Taken together, our findings reveal circTXNRD1 as a novel inflammatory mediator in PM-induced inflammation in HBECs via regulating miR-892a/COX-2 axis. These results provide new insight into the biological mechanism underlying PM-induced inflammation in chronic airway diseases. [Display omitted] • The differential circRNAs expression profile was identified in PM-exposed HBECs. • The circTXNRD1 was significantly upregulated by PM in HBECs. • The circTXNRD1 promoted PM-induced inflammation via miR-892a/COX-2 axis in HBECs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00456535
Volume :
286
Database :
Academic Search Index
Journal :
Chemosphere
Publication Type :
Academic Journal
Accession number :
153374067
Full Text :
https://doi.org/10.1016/j.chemosphere.2021.131614