安普克
医学
基因敲除
炎症体
吡喃结构域
下调和上调
强直性脊柱炎
信号转导
调节器
蛋白激酶A
细胞生物学
癌症研究
激酶
免疫学
基因
生物
炎症
遗传学
作者
Ruiyang Fu,Xiaoqing Guo,Zhongqiang Pan,Yaling Wang,Jing Xu,Lei Zhang,Jinxia Li
标识
DOI:10.1186/s13018-023-04200-x
摘要
Investigate the AMPK (protein kinase AMP-activated catalytic subunit alpha 1)/YAP (Yes1 associated transcriptional regulator)/NLRP3 (NLR family pyrin domain containing 3) signaling pathway's role in ankylosing spondylitis (AS) development using public database analysis, in vitro and in vivo experiments.Retrieve AS dataset, analyze differential gene expression in R, conduct functional enrichment analysis, collect 30 AS patient and 30 normal control samples, and construct a mouse model. ELISA, IP, and knockdown experiments were performed to detect expression changes.NLRP3 was identified as a significant AS-related gene. Caspase-1, IL-1β, IL-17A, IL-18, IL-23, YAP, and NLRP3 were upregulated in AS patients. Overexpressing AMPK inhibited YAP's blockade on NLRP3 ubiquitination, reducing ossification in fibroblasts. Inhibiting AMPK exacerbated AS symptoms in AS mice.AMPK may suppress YAP expression, leading to NLRP3 inflammasome inhibition and AS alleviation.
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