MiR-21 involve in ERK-mediated upregulation of MMP9 in the rat hippocampus following cerebral ischemia

被引:48
作者
Deng, XiaHeng [1 ,2 ]
Zhong, Yun [2 ]
Gu, LiZe [2 ,3 ]
Shen, Wei [1 ]
Guo, Jun [2 ,3 ]
机构
[1] Huazhong Univ Sci & Technol, Dept Neurol, Puai Hosp, Tongji Med Coll, Wuhan 430033, Peoples R China
[2] Nanjing Med Univ, Lab Ctr Basic Med Sci, Nanjing 210029, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Dept Biochem & Mol Biol, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Cerebral ischemia; miRNA; MMP9; ERIC; HEPATOCELLULAR-CARCINOMA; EXPRESSION; MATRIX-METALLOPROTEINASE-9; ACTIVATION; INVASION; CANCER; IDENTIFICATION; INHIBITION; MICRORNAS; KINASES;
D O I
10.1016/j.brainresbull.2013.02.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Matrix metallinoprotease-9 (MMP9) plays a key role in the pathogenesis of post-ischemic blood brain barrier (BBB) disruption and the formation of lesions after cerebral ischemia. In this study we investigate the effect of brain-specific miRNAs on MMP-9 protein level in the rat hippocampus following cerebral ischemia and its underlying mechanism. Cerebral ischemia significantly upregulated miR-21 and -224 in the hippocampus; however, expression of miR-122 and -338-3p was not significantly affected by ischemia. Silencing of miR-21, but not -224, reduced MMP9 protein level after cerebral ischemia. Downregulation of extracellular signal-regulated kinase (ERK) signaling using the ERK inhibitor U0126 and the calcium-channel blocker ketamine inhibited the upregulation of miR-21 expression and MMP9 protein level after cerebral ischemia. The study suggests that cerebral ischemia up-regulates expression level of miR-21, which is involved in ERIC-stimulated upregulation of MMP9 following cerebral ischemia via a calcium-dependent mechanism. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:56 / 62
页数:7
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