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The IL1β-HER2-CLDN18/CLDN4 axis mediates lung barrier damage in ARDS

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成果类型:
期刊论文
作者:
Ma, Xinhua;Yu, Xin;Zhou, Qi
通讯作者:
Ma, XH
作者机构:
[Ma, Xinhua] Cent South Univ, Xiangya Hosp, Dept Intens Care Unit, Changsha, Peoples R China.
[Yu, Xin] China Japan Friendship Hosp, Ctr Resp Dis, Natl Clin Res Ctr Resp Dis, Dept Pulm & Crit Care Med, Beijing, Peoples R China.
[Zhou, Qi] Hunan Univ Tradit Chinese Med, Dept Anesthesiol, Affiliated Hosp 1, Changsha, Peoples R China.
通讯机构:
[Ma, XH ] C
Cent South Univ, Xiangya Hosp, Dept Intens Care Unit, Changsha, Peoples R China.
语种:
英文
关键词:
HER2;IL-1beta;acute respiratory distress syndrome;claudin18;lung barrier injury
期刊:
AGING-US
ISSN:
1945-4589
年:
2020
卷:
12
期:
4
页码:
3249-3265
基金类别:
The authors would like to thank the Life-Ontology Biological Technology Co., Ltd for assisting with bioinformatics analysis. This work was supported by Hunan Natural Science Foundation (Grant number: 2017JJ2375).
机构署名:
本校为其他机构
院系归属:
第一中医临床学院
摘要:
Objective: The high mortality rate associated with acute respiratory distress syndrome (ARDS) is a major challenge for intensive care units. In the present study, we applied bioinformatics and animal models to identify core genes and potential corresponding pathways in ARDS. Results: Using bioinformatics analysis, IL-1 beta was identified as the core gene of ARDS. Cell experiments showed that up-regulation of IL-1 beta downregulates claudin18 to promote lung barrier function damage by regulating the IL-1 beta-HER2/HER3 axis, further promoting the development of ARDS. This was validated in the ...

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