LincRNA Cox-2 Regulates Lipopolysaccharide-Induced Inflammatory Response of Human Peritoneal Mesothelial Cells via Modulating miR-21/NF-κB Axis

Postoperative peritoneal adhesion (PPA) is a common postoperative complication caused by any peritoneal inflammatory process. This study aimed to identify the biological function of large intergenic non-coding RNAs (lincRNAs) Cox-2 in the inflammation reaction of adhesion formation. The Cox-2 expres...

Full description

Saved in:
Bibliographic Details
Main Authors: Yaoyao Bian, Lili Yang, Bin Zhang, Wen Li, Sen Wang, Shuling Jiang, Xi Chen, Wenlin Li, Li Zeng
Format: Article
Language:English
Published: Wiley 2019-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2019/8626703
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832564828261056512
author Yaoyao Bian
Lili Yang
Bin Zhang
Wen Li
Sen Wang
Shuling Jiang
Xi Chen
Wenlin Li
Li Zeng
author_facet Yaoyao Bian
Lili Yang
Bin Zhang
Wen Li
Sen Wang
Shuling Jiang
Xi Chen
Wenlin Li
Li Zeng
author_sort Yaoyao Bian
collection DOAJ
description Postoperative peritoneal adhesion (PPA) is a common postoperative complication caused by any peritoneal inflammatory process. This study aimed to identify the biological function of large intergenic non-coding RNAs (lincRNAs) Cox-2 in the inflammation reaction of adhesion formation. The Cox-2 expression in peritoneal adhesion tissues and normal tissues was detected. The human peritoneal mesothelium cells (HPMCs) were treated with lipopolysaccharide (LPS) to induce inflammatory injury. The effect of Cox-2 suppression on cell viability, apoptosis and inflammatory factors of LPS induced HPMCs injury were explored. The regulatory correlation between Cox-2 and miR-21, as well as the targeted genes of miR-21 were identified. Meanwhile, the regulatory mechanism of Cox-2/miR-21 axis on NF-κB pathway was explored. It indicated that Cox-2 was highly expressed in peritoneal adhesion tissues compared with that in normal tissues. Suppression of Cox-2 ameliorated LPS induced HMPCs injury as cell viability was promoted, and cell apoptosis and the production of inflammatory factors were inhibited. And suppression of Cox-2 reversed the LPS induced HPMCs injury by regulation of miR-21 negatively. miR-21 was negatively correlated with TLR4, and TLR4 was predicted as target gene of miR-21. Furthermore, the suppression of miR-21 on LPS induced HPMCs injury was reversed by knockdown of TLR4, which could inhibited the activation of NF-κB pathway axis. It suggested that the effect of Cox-2 on LPS induced HPMCs injury was achieved by negatively regulation of miR-21 and targeted TLR4 through NF-κB pathway axis. The findings may provide a new insight into preventing postoperative peritoneal adhesion.
format Article
id doaj-art-7b7bfc2d429344ddacb6698d194e0710
institution Kabale University
issn 0962-9351
1466-1861
language English
publishDate 2019-01-01
publisher Wiley
record_format Article
series Mediators of Inflammation
spelling doaj-art-7b7bfc2d429344ddacb6698d194e07102025-02-03T01:10:06ZengWileyMediators of Inflammation0962-93511466-18612019-01-01201910.1155/2019/86267038626703LincRNA Cox-2 Regulates Lipopolysaccharide-Induced Inflammatory Response of Human Peritoneal Mesothelial Cells via Modulating miR-21/NF-κB AxisYaoyao Bian0Lili Yang1Bin Zhang2Wen Li3Sen Wang4Shuling Jiang5Xi Chen6Wenlin Li7Li Zeng8School of Nursing, Nanjing University of Chinese Medicine, Nanjing, ChinaSchool of First Clinical Medicine, Nanjing University of Chinese Medicine, Nanjing, ChinaDigestive Department, Ningbo Hospital of traditional Chinese Medicine, Ningbo, ChinaSchool of Preclinical Medicine, Guiyang University of Chinese Medicine, Guiyang, ChinaDepartment of Anorectal, Huainan Second People's Hospital, Huainan, ChinaSchool of Nursing, Nanjing University of Chinese Medicine, Nanjing, ChinaSchool of Nursing, Nanjing University of Chinese Medicine, Nanjing, ChinaJingwen Library, Nanjing University of Chinese Medicine, Nanjing, ChinaSchool of First Clinical Medicine, Nanjing University of Chinese Medicine, Nanjing, ChinaPostoperative peritoneal adhesion (PPA) is a common postoperative complication caused by any peritoneal inflammatory process. This study aimed to identify the biological function of large intergenic non-coding RNAs (lincRNAs) Cox-2 in the inflammation reaction of adhesion formation. The Cox-2 expression in peritoneal adhesion tissues and normal tissues was detected. The human peritoneal mesothelium cells (HPMCs) were treated with lipopolysaccharide (LPS) to induce inflammatory injury. The effect of Cox-2 suppression on cell viability, apoptosis and inflammatory factors of LPS induced HPMCs injury were explored. The regulatory correlation between Cox-2 and miR-21, as well as the targeted genes of miR-21 were identified. Meanwhile, the regulatory mechanism of Cox-2/miR-21 axis on NF-κB pathway was explored. It indicated that Cox-2 was highly expressed in peritoneal adhesion tissues compared with that in normal tissues. Suppression of Cox-2 ameliorated LPS induced HMPCs injury as cell viability was promoted, and cell apoptosis and the production of inflammatory factors were inhibited. And suppression of Cox-2 reversed the LPS induced HPMCs injury by regulation of miR-21 negatively. miR-21 was negatively correlated with TLR4, and TLR4 was predicted as target gene of miR-21. Furthermore, the suppression of miR-21 on LPS induced HPMCs injury was reversed by knockdown of TLR4, which could inhibited the activation of NF-κB pathway axis. It suggested that the effect of Cox-2 on LPS induced HPMCs injury was achieved by negatively regulation of miR-21 and targeted TLR4 through NF-κB pathway axis. The findings may provide a new insight into preventing postoperative peritoneal adhesion.http://dx.doi.org/10.1155/2019/8626703
spellingShingle Yaoyao Bian
Lili Yang
Bin Zhang
Wen Li
Sen Wang
Shuling Jiang
Xi Chen
Wenlin Li
Li Zeng
LincRNA Cox-2 Regulates Lipopolysaccharide-Induced Inflammatory Response of Human Peritoneal Mesothelial Cells via Modulating miR-21/NF-κB Axis
Mediators of Inflammation
title LincRNA Cox-2 Regulates Lipopolysaccharide-Induced Inflammatory Response of Human Peritoneal Mesothelial Cells via Modulating miR-21/NF-κB Axis
title_full LincRNA Cox-2 Regulates Lipopolysaccharide-Induced Inflammatory Response of Human Peritoneal Mesothelial Cells via Modulating miR-21/NF-κB Axis
title_fullStr LincRNA Cox-2 Regulates Lipopolysaccharide-Induced Inflammatory Response of Human Peritoneal Mesothelial Cells via Modulating miR-21/NF-κB Axis
title_full_unstemmed LincRNA Cox-2 Regulates Lipopolysaccharide-Induced Inflammatory Response of Human Peritoneal Mesothelial Cells via Modulating miR-21/NF-κB Axis
title_short LincRNA Cox-2 Regulates Lipopolysaccharide-Induced Inflammatory Response of Human Peritoneal Mesothelial Cells via Modulating miR-21/NF-κB Axis
title_sort lincrna cox 2 regulates lipopolysaccharide induced inflammatory response of human peritoneal mesothelial cells via modulating mir 21 nf κb axis
url http://dx.doi.org/10.1155/2019/8626703
work_keys_str_mv AT yaoyaobian lincrnacox2regulateslipopolysaccharideinducedinflammatoryresponseofhumanperitonealmesothelialcellsviamodulatingmir21nfkbaxis
AT liliyang lincrnacox2regulateslipopolysaccharideinducedinflammatoryresponseofhumanperitonealmesothelialcellsviamodulatingmir21nfkbaxis
AT binzhang lincrnacox2regulateslipopolysaccharideinducedinflammatoryresponseofhumanperitonealmesothelialcellsviamodulatingmir21nfkbaxis
AT wenli lincrnacox2regulateslipopolysaccharideinducedinflammatoryresponseofhumanperitonealmesothelialcellsviamodulatingmir21nfkbaxis
AT senwang lincrnacox2regulateslipopolysaccharideinducedinflammatoryresponseofhumanperitonealmesothelialcellsviamodulatingmir21nfkbaxis
AT shulingjiang lincrnacox2regulateslipopolysaccharideinducedinflammatoryresponseofhumanperitonealmesothelialcellsviamodulatingmir21nfkbaxis
AT xichen lincrnacox2regulateslipopolysaccharideinducedinflammatoryresponseofhumanperitonealmesothelialcellsviamodulatingmir21nfkbaxis
AT wenlinli lincrnacox2regulateslipopolysaccharideinducedinflammatoryresponseofhumanperitonealmesothelialcellsviamodulatingmir21nfkbaxis
AT lizeng lincrnacox2regulateslipopolysaccharideinducedinflammatoryresponseofhumanperitonealmesothelialcellsviamodulatingmir21nfkbaxis