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miR-146a 在重症肌无力中的表达改变。

Altered expression of miR-146a in myasthenia gravis.

机构信息

Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410078, China; Department of Biochemistry and Molecular Biology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.

出版信息

Neurosci Lett. 2013 Oct 25;555:85-90. doi: 10.1016/j.neulet.2013.09.014. Epub 2013 Sep 13.

Abstract

The purpose of this study was to analyze the expression of miR-146a in PBMCs obtained from patients with myasthenia gravis (MG) and healthy controls and to investigate the effect of the inhibition of miR-146a on the activation of AchR specific B cells obtained from mice. The expression of miR-146a levels in PBMCs obtained from patients with MG and healthy controls were determined by qRT-PCR. MiR-146a's complementary fragment, AntagomiR-146a, was synthesized as inhibitor, and the nonfunctional fragment, which has similar construction to AntagomiR-146a, was synthesized as negative control inhibitor. The expression of miR-146a, CD40, CD80 and CD86 on AchR specific B cells were analyzed by qRT-PCR and flow cytometry. Western blotting was used to detect the expression of TLR4, NF-κB and Bcl-2 .The expression of miRNA-146a in PBMCs obtained from patients with MG was significantly upregulated compared to healthy controls (P<0.01). Transfection with miR-146a inhibitor dramatically decreased expression of miR-146a, CD40, CD80, TLR4 and NF-κB on AchR specific B cells compared to mock transfected cells. We conclude that abnormal expression/regulation of miR-146a may play an important role in the regulation of AchR specific B cells and contribute to the pathogenesis of MG.

摘要

本研究旨在分析重症肌无力(MG)患者和健康对照者外周血单个核细胞(PBMCs)中 miR-146a 的表达,并探讨抑制 miR-146a 对从小鼠中获得的乙酰胆碱受体(AchR)特异性 B 细胞激活的影响。通过 qRT-PCR 测定 MG 患者和健康对照者 PBMCs 中 miR-146a 水平的表达。合成 miR-146a 的互补片段 AntagomiR-146a 作为抑制剂,合成具有与 AntagomiR-146a 相似结构的非功能片段作为阴性对照抑制剂。通过 qRT-PCR 和流式细胞术分析 AchR 特异性 B 细胞中 miR-146a、CD40、CD80 和 CD86 的表达。Western blot 检测 TLR4、NF-κB 和 Bcl-2 的表达。与健康对照组相比,MG 患者 PBMCs 中 miR-146a 的表达明显上调(P<0.01)。与 mock 转染细胞相比,转染 miR-146a 抑制剂后,AchR 特异性 B 细胞中 miR-146a、CD40、CD80、TLR4 和 NF-κB 的表达显著降低。我们得出结论,miR-146a 的异常表达/调节可能在调节 AchR 特异性 B 细胞中发挥重要作用,并有助于 MG 的发病机制。

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