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关于RNA结合基序(RNP1、RRM)蛋白3(RBM3)作为双相情感障碍患者锂反应潜在生物标志物的证据。

Evidence towards RNA Binding Motif (RNP1, RRM) Protein 3 (RBM3) as a Potential Biomarker of Lithium Response in Bipolar Disorder Patients.

作者信息

Papadima Eleni Merkouri, Niola Paola, Melis Carla, Pisanu Claudia, Congiu Donatella, Cruceanu Cristiana, Lopez Juan Pablo, Turecki Gustavo, Ardau Raffaella, Severino Giovanni, Chillotti Caterina, Del Zompo Maria, Squassina Alessio

机构信息

Department of Biomedical Sciences, Section of Neuroscience and Clinical Pharmacology, School of Medicine, University of Cagliari, sp 6, 09042, Cagliari, Italy.

McGill Group for Suicide Studies, Douglas Mental Health University Institute, McGill University, Montreal, QC, Canada.

出版信息

J Mol Neurosci. 2017 Aug;62(3-4):304-308. doi: 10.1007/s12031-017-0938-5. Epub 2017 Jun 14.

Abstract

Lithium has been used for more than six decades for the management of bipolar disorder (BD). In a previous transcriptomic study, we showed that patients affected by either BD or cluster headache, both disorders characterized by circadian disturbances and response to lithium in a subgroup of patients, have higher expression of the RNA binding motif (RNP1, RRM) protein 3 (RBM3) gene compared to controls. To investigate whether RBM3 could represent a biomarker of lithium response, we screened raw microarray expression data from lymphoblastoid cell lines (LCLs) derived from 20 BD patients, responders or non-responders to lithium. RBM3 was the most significantly differentially expressed gene in the list, being overexpressed in responders compared to non-responders (fold change = 2.0; p = 1.5 × 10). We therefore sought to validate the microarray finding by quantitative reverse transcription polymerase chain reaction (RT-qPCR) and explore whether RBM3 expression was modulated by lithium treatment in vitro in LCLs as well as in human-derived neural progenitor cells (NPCs). Our findings confirmed the higher expression of RBM3 in responders compared to non-responders (fold change = 3.78; p = 0.0002). Lithium did not change RBM3 expression in LCLs in any of the groups, but it increased its expression in NPCs. While preliminary, our data suggest that higher levels of RBM3 might be required for better lithium response and that the expression of this gene could be modulated by lithium in a tissue-specific manner.

摘要

锂用于双相情感障碍(BD)的治疗已有六十多年。在之前的一项转录组学研究中,我们发现,双相情感障碍或丛集性头痛患者(这两种疾病均以昼夜节律紊乱为特征,且部分患者对锂有反应)的RNA结合基序(RNP1,RRM)蛋白3(RBM3)基因表达高于对照组。为了研究RBM3是否可作为锂反应的生物标志物,我们筛选了来自20例双相情感障碍患者的淋巴母细胞系(LCL)的原始微阵列表达数据,这些患者对锂治疗有反应或无反应。RBM3是列表中差异表达最显著的基因,与无反应者相比,反应者中该基因过度表达(倍数变化=2.0;p=1.5×10)。因此,我们试图通过定量逆转录聚合酶链反应(RT-qPCR)验证微阵列研究结果,并探讨锂处理是否在体外对LCL以及人源神经祖细胞(NPC)中的RBM3表达有调节作用。我们的研究结果证实,与无反应者相比,反应者中RBM3表达更高(倍数变化=3.78;p=0.0002)。在任何组中,锂均未改变LCL中RBM3的表达,但增加了NPC中RBM3的表达。虽然是初步研究,但我们的数据表明,更好的锂反应可能需要更高水平的RBM3,且该基因的表达可能受锂以组织特异性方式调节。

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