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Lef1 is transcriptionally activated by Klf4 and suppresses hyperoxia-induced alveolar epithelial cell injury

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成果类型:
期刊论文
作者:
Yang, Min;Huang, Xueshan;Shen, Fang;Yi, Juanjuan;Meng, Yanni;...
通讯作者:
Yanping Chen
作者机构:
[Yang, Min; Meng, Yanni; Chen, Yanping] Hunan Childrens Hosp, Dept Resp, 86 Ziyuan Rd, Changsha 410007, Hunan, Peoples R China.
[Huang, Xueshan] Univ South China, Hengyang, Peoples R China.
[Shen, Fang] Hunan Childrens Hosp, Res Inst Children, Changsha, Peoples R China.
[Yi, Juanjuan] Hunan Childrens Hosp, Dept Neonate, Changsha, Peoples R China.
通讯机构:
[Yanping Chen] D
Department of Respiratory, Hunan Children’s Hospital, No. 86 Ziyuan Road, Hunan Province, Changsha, China
语种:
英文
关键词:
Alveolar epithelial cell injury;Bronchopulmonary dysplasia;hyperoxia;Klf4;Lef1
期刊:
Experimental Lung Research
ISSN:
0190-2148
年:
2022
卷:
48
期:
7-8
页码:
213-223
基金类别:
This work was supported by Youth Fund of Hunan Natural Science Foundation (2019JJ50293) and Hunan Health Commission (B2019012). Thanks to the members of our laboratory for their contributions.
机构署名:
本校为其他机构
摘要:
Purpose: Bronchopulmonary dysplasia (BPD) is a long-term respiratory condition. More than a quarter of extremely premature newborns are harmed by BPD. At present, there are no apparent effective drugs or treatments for the condition. In this study, we aimed to investigate the functional role and mechanism of lymphoid enhancer-binding factor 1 (Lef1) in BPD in vitro. Materials and Methods: Blood samples from BPD patients and healthy volunteers were gathered, and an in vitro model of BPD was developed in alveolar epithelial cells (AECs) MLE-12 in...

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