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本文引用的文献

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Evidence for selective microRNAs and their effectors as common long-term targets for the actions of mood stabilizers.选择性微小RNA及其效应分子作为心境稳定剂作用的常见长期靶点的证据。
Neuropsychopharmacology. 2009 May;34(6):1395-405. doi: 10.1038/npp.2008.131. Epub 2008 Aug 13.
2
Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein.FGF20的miRNA - 433结合位点变异通过α-突触核蛋白的过表达赋予帕金森病风险。
Am J Hum Genet. 2008 Feb;82(2):283-9. doi: 10.1016/j.ajhg.2007.09.021. Epub 2008 Jan 31.
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Discriminating single-base difference miRNA expressions using microarray Probe Design Guru (ProDeG).使用微阵列探针设计专家系统(ProDeG)区分单碱基差异的miRNA表达。
Nucleic Acids Res. 2008 Mar;36(5):e27. doi: 10.1093/nar/gkm1165. Epub 2008 Jan 21.
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microRNAs: small molecules with big roles - C. elegans to human cancer.微小RNA:作用重大的小分子——从秀丽隐杆线虫到人类癌症
Biol Cell. 2008 Feb;100(2):71-81. doi: 10.1042/BC20070078.
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Mechanisms of post-transcriptional regulation by microRNAs: are the answers in sight?微小RNA介导的转录后调控机制:答案近在眼前了吗?
Nat Rev Genet. 2008 Feb;9(2):102-14. doi: 10.1038/nrg2290.
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Getting to the root of miRNA-mediated gene silencing.探寻miRNA介导的基因沉默的根源。
Cell. 2008 Jan 11;132(1):9-14. doi: 10.1016/j.cell.2007.12.024.
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Dysregulation of miRNA 181b in the temporal cortex in schizophrenia.精神分裂症患者颞叶皮质中miRNA 181b的失调
Hum Mol Genet. 2008 Apr 15;17(8):1156-68. doi: 10.1093/hmg/ddn005. Epub 2008 Jan 9.
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Lithium salts in the treatment of psychotic excitement.锂盐治疗精神病性兴奋。
Med J Aust. 1949 Sep 3;2(10):349-52. doi: 10.1080/j.1440-1614.1999.06241.x.
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miRBase: tools for microRNA genomics.miRBase:用于微小RNA基因组学的工具。
Nucleic Acids Res. 2008 Jan;36(Database issue):D154-8. doi: 10.1093/nar/gkm952. Epub 2007 Nov 8.
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Brain expressed microRNAs implicated in schizophrenia etiology.大脑表达的 microRNAs 与精神分裂症的病因有关。
PLoS One. 2007 Sep 12;2(9):e873. doi: 10.1371/journal.pone.0000873.

锂处理对淋巴母细胞系中 microRNA 表达的变化。

MicroRNA expression changes in lymphoblastoid cell lines in response to lithium treatment.

机构信息

Department of Psychiatry, University of Michigan Medical School, Ann Arbor, MI 48109, USA.

出版信息

Int J Neuropsychopharmacol. 2009 Aug;12(7):975-81. doi: 10.1017/S1461145709000029. Epub 2009 Mar 2.

DOI:10.1017/S1461145709000029
PMID:19254429
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3216398/
Abstract

Lithium (Li) is commonly used in the treatment of bipolar disorder (BD). However, the molecular mechanism of its action is not completely understood. MicroRNAs (miRNAs), a class of small RNA species are recognized as important regulators in post-transcription gene expression. To explore the role of miRNAs in Li's action, we quantitatively analysed the expression patterns of 13 miRNAs in 20 lymphoblastoid cell lines (LCLs) with or without Li treatment in culture. Using paired t statistics in the analysis, we identified significant changes in seven of the 13 miRNAs tested in LCLs sampled at treatment day 4 (p<0.05). Four of the seven significant miRNAs, miR-34a, miR-152, miR-155, and miR-221 consistently changed expression in the same LCLs at a longer treatment time-point, day 16 (Bonferroni p<0.05). Interestingly, miR-221 and miR-34a also changed expression in rat hippocampus in response to Li treatment (Zhou et al. 2008), although in the opposite direction. We focused on the predicted target mRNAs of miR-221 and miR-34a, and identified 29 and ten targets that were strongly and inversely correlated to expression with the two miRNAs, respectively. Our results suggest that miRNAs are excellent candidates for the study of the molecular basis of Li's treatment action in cell systems such as lymphocytes given limited access to the human brain.

摘要

锂(Li)常用于治疗双相情感障碍(BD)。然而,其作用的分子机制尚不完全清楚。微小 RNA(miRNAs)是一类小 RNA 物种,被认为是转录后基因表达的重要调节因子。为了探讨 miRNAs 在 Li 作用中的作用,我们定量分析了培养过程中有或没有 Li 处理的 20 个淋巴母细胞系(LCL)中 13 种 miRNAs 的表达模式。在分析中使用配对 t 检验,我们在处理第 4 天(p<0.05)的 LCL 中鉴定出 13 种测试 miRNA 中有 7 种的表达发生了显著变化。在更长的处理时间点,第 16 天(Bonferroni p<0.05),这 7 个显著 miRNA 中的 4 个,miR-34a、miR-152、miR-155 和 miR-221,在相同的 LCL 中表现出一致的表达变化。有趣的是,miR-221 和 miR-34a 在大鼠海马体中也对 Li 处理有反应(Zhou 等人,2008),尽管表达方向相反。我们关注 miR-221 和 miR-34a 的预测靶 mRNAs,并确定了 29 和 10 个靶基因,它们与这两个 miRNA 的表达呈强烈的负相关。我们的结果表明,miRNAs 是研究 Li 治疗作用在淋巴细胞等细胞系统中分子基础的优秀候选者,因为这些细胞系统对人脑的接触有限。