一氧化氮合酶
基因沉默
小RNA
化学
荧光素酶
转染
下调和上调
NF-κB
调节器
发病机制
细胞生物学
三素数非翻译区
分子生物学
一氧化氮
信号转导
非翻译区
信使核糖核酸
生物
基因
生物化学
免疫学
有机化学
作者
Zafar Rasheed,Hani A. Al‐Shobaili,Naila Rasheed,Amer Mahmood,Michael A. Khan
标识
DOI:10.1016/j.abb.2016.02.003
摘要
Inducible nitric oxide synthase (iNOS) expression is associated with the pathogenesis of osteoarthritis (OA). This study was undertaken to investigate whether interleukin-1β (IL-1β)-mediated induction of iNOS can be regulated by microRNA-26a-5p (hsa-miR-26a-5p) in OA. Bioinformatics approaches show that 3′UTR of iNOS mRNA contained the ‘seed-matched-sequence’ for hsa-miR-26a-5p. IL-1β-induced expression of iNOS correlated with the down-regulation of miR-26a-5p in human OA chondrocytes. hsa-miR-26a-5p directly suppressed the luciferase activity of 3′UTR-iNOS reporter clone. Transfection with pre-miR-26a-5p induced marked silencing of iNOS expression. Activation of NF-κB pathway down-regulated the expression of hsa-miR-26a-5p and induced iNOS expression. In short, this is the first report that shows hsa-miR-26a-5p is a direct regulator of iNOS expression in human chondrocytes. hsa-miR-26a-5p may be an important regulator of human cartilage homeostasis and a new target for OA therapy.
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