小胶质细胞
缺血性损伤
缺血性中风
微阵列
冲程(发动机)
炎症体
微阵列分析技术
调节器
脑卒中
细胞生物学
神经科学
生物
基因表达
癌症研究
医学
缺血
基因
炎症
免疫学
内科学
生物化学
工程类
机械工程
作者
Yunhua Zang,Xiyan Zhou,Qun Wang,Xia Li,Hailiang Huang
标识
DOI:10.1016/j.bbrc.2018.04.194
摘要
Stroke is one of the leading causes for serious long-term neurological disability. LncRNAs have been investigated to be dysregulated in ischemic stroke. However, the underlying mechanisms of some specific lncRNAs have not been clearly clarified. To determine lncRNA-mediated regulatory mechanism in ischemic stroke, we constructed OGD/R injury model of cerebral microglial cells. Microarray analysis was carried out and analyzed that lncRNA functional intergenic repeating RNA element (FIRRE) was associated with OGD/R injury. Based on the molecular biotechnology, we demonstrated that FIRRE could activate NF-kB signal pathway. Meanwhile, the activated NF-kB promoted FIRRE expression in OGD/R-treated cerebral microglial cells. Therefore, FIRRE and NF-kB formed a positive feedback loop to promote the transcription of NLRP3 inflammasome, thus contributed to the OGD/R injury of cerebral microglial cells. All findings in this study may help to explore novel and specific therapeutic target for ischemic stroke.
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