LINC00665/miR-132-5p Reduces Inflammation in Epileptic Cells by Targeting MAPK3.

IF 1.6 3区 医学 Q3 GENETICS & HEREDITY
Qi-Ming Pang, Cui Wang, Bang-Tao Li, Su-Li Zhang, Jiao-Yang Li, Shuo Gu
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引用次数: 0

Abstract

To investigate the role of miR-132-5p in the inflammatory response in epilepsy. Peripheral blood was collected from epileptic and healthy children, and the expression of LINC00665 and miR-132-5p was detected by q-PCR. Epilepsy cell models were constructed with microglia, transfected with miR-132-5p inhibitor and NC, and the expression of LINC00665 and miR-132-5p was detected by q-PCR, the expression of TNF-α, IL-1β, and IL-6 in the cell supernatant was detected by ELISA, and the protein levels of NLRP3 and MAPK3 were detected by WB. Finally, the targeting relationship between LINC00665 and miR-132-5p was verified by dual luciferase assay. The expression levels of both LINC00665 and miR-132-5p in the peripheral blood of children with epilepsy were significantly higher than those of healthy children. After transfection of epileptic cells with miR-132-5p inhibitor, the expression levels of LINC00665 and miR-132-5p were increased, and the expression levels of TNF-α, IL-1β, IL-6, NLRP3, and MAPK3 were decreased. Dual luciferase assay showed targeted binding of LINC00665 and miR-132-5p. LINC00665/miR-132-5p attenuates inflammatory responses in epileptic cells by targeting MAPK3.

LINC00665/miR-132-5p通过靶向MAPK3减少癫痫细胞的炎症
探讨miR-132-5p在癫痫患者炎症反应中的作用。采集癫痫患儿和健康患儿外周血,采用q-PCR检测LINC00665和miR-132-5p的表达。用小胶质细胞构建癫痫细胞模型,转染miR-132-5p抑制剂和NC,采用q-PCR检测LINC00665和miR-132-5p的表达,ELISA检测细胞上清中TNF-α、IL-1β和IL-6的表达,WB检测NLRP3和MAPK3蛋白水平。最后,通过双荧光素酶实验验证LINC00665与miR-132-5p的靶向关系。癫痫患儿外周血中LINC00665和miR-132-5p的表达水平均显著高于健康儿童。转染miR-132-5p抑制剂后,癫痫细胞中LINC00665、miR-132-5p表达水平升高,TNF-α、IL-1β、IL-6、NLRP3、MAPK3表达水平降低。双荧光素酶检测显示LINC00665与miR-132-5p靶向结合。LINC00665/miR-132-5p通过靶向MAPK3减轻癫痫细胞的炎症反应。
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来源期刊
CiteScore
5.90
自引率
7.10%
发文量
40
审稿时长
4-8 weeks
期刊介绍: Neuropsychiatric Genetics, Part B of the American Journal of Medical Genetics (AJMG) , provides a forum for experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. It is a resource for novel genetics studies of the heritable nature of psychiatric and other nervous system disorders, characterized at the molecular, cellular or behavior levels. Neuropsychiatric Genetics publishes eight times per year.
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