RNA干扰
缺氧(环境)
生物
肺动脉
细胞凋亡
癌症研究
分子生物学
核糖核酸
基因
医学
化学
内科学
生物化学
有机化学
氧气
作者
Peng Wen,Weile Fang,Xiaona Gao,Xiaoquan Guo,Guyue Li,Fengping Guo,Guoliang Hu,Yu Zhuang,Lin Li,Chenxi Jiang,Ping Liu
出处
期刊:Poultry Science
[Elsevier BV]
日期:2023-12-18
卷期号:103 (5): 103388-103388
被引量:1
标识
DOI:10.1016/j.psj.2023.103388
摘要
Pulmonary artery remodeling is a characteristic feature of broiler ascites syndrome(BAS). Pulmonary artery endothelial cells (PAECs) regulated by HIF-1α play a critical role in pulmonary artery remodeling, but the underlying mechanisms of HIF-1α in BAS remain unclear. In this experiment, primary PAECs were cultured in vitro and were identified by coagulation factor VIII. After hypoxia and RNA interference, The mRNA and protein expression levels of HIF-1α and VEGF were determined by qPCR and Western blotting. The transcriptome profiles of PAECs were obtained by RNA sequencing. Our results showed that the positive rate of PAECs was more than 90%, hypoxia-induced promoted the proliferation and apoptosis of PAECs, and RNA interference significantly downregulated the expression of HIF-1α, inhibited the proliferation of PAECs, and promoted the apoptosis of PAECs. In addition, transcriptome sequencing analysis indicated that HIF-1α may regulate broiler ascites syndrome by mediating COL4A, vitronectin, vWF, ITGα8, and MKP-5 in the ECM, CAMs and MAPK pathways in PAECs. These studies lay the foundation for further exploration of the mechanisms of pulmonary artery remodeling, and HIF-1α may be a potentially effective gene for the prevention and treatment of BAS.
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