Department of Biological Sciences, National Sun Yat-sen University, No. 70, Lienhai Rd., Gushan Dist., Kaohsiung City, 80424, Taiwan.
Department of Anesthesiology, E-Da Hospital/I-Shou University, Kaohsiung City, Taiwan.
Eur J Neurosci. 2017 Dec;46(11):2713-2728. doi: 10.1111/ejn.13745. Epub 2017 Nov 6.
Recent studies using microarray-based approaches have demonstrated that microRNAs (miRNAs) are involved in pain processing pathways. However, a significant proportion of computational predictions of miRNA targets are false-positive interactions. To increase the chance of identifying biologically relevant targets, we performed an integrated analysis of both miRNA and mRNA expression profiles in the rat spinal cord during complete Freund's adjuvant (CFA)-induced inflammatory pain. We generated miRNA and mRNA arrays from the same corresponding samples on days 5 and 14 after CFA injection. Five miRNAs and 1096 mRNAs in the CFA 5d group and 16 miRNAs and 647 mRNAs in the CFA 14d group were differentially expressed based on a filter of at least a 1.5-fold change in either direction. An integrated analysis revealed 54 mRNA targets with an inverse correlation to the expression patterns of three miRNAs in the CFA 5d group. Seventy-five targets were inversely correlated to six miRNAs in the CFA 14d group. The miRNA-mRNA interaction networks revealed significant changes in miR-124, miR-149, miR-3584 and their target genes, IL-6R, ADAM19, LAMC1 and CERS2, in the CFA 5d group. In the CFA 14d group, significant changes were noted in miR-124, miR-29, miR-34, miR-30, miR-338 and their target genes, TIMP2, CREB5 and EFNB1. We also investigated an interaction pair, miR-124-3p and IL-6R, and the results showed that miR-124-3p could attenuate inflammatory pain and decrease IL-6R expression in the spinal cord. These specific miRNAs and their target genes provide possible avenues for the diagnosis and treatment of inflammatory pain.
最近使用基于微阵列的方法的研究表明,microRNAs (miRNAs) 参与疼痛处理途径。然而,计算预测的 miRNA 靶标的很大一部分是假阳性相互作用。为了增加识别具有生物学相关性的靶标的机会,我们对完全弗氏佐剂 (CFA) 诱导的炎症性疼痛大鼠脊髓中的 miRNA 和 mRNA 表达谱进行了综合分析。我们在 CFA 注射后第 5 天和第 14 天从相同的对应样本中生成 miRNA 和 mRNA 阵列。CFA 5d 组中有 5 个 miRNA 和 1096 个 mRNA,CFA 14d 组中有 16 个 miRNA 和 647 个 mRNA 根据至少 1.5 倍变化的过滤器显示差异表达。综合分析显示,CFA 5d 组中有 54 个 mRNA 靶标与三个 miRNA 的表达模式呈负相关。CFA 14d 组中有 75 个靶标与六个 miRNA 呈负相关。miRNA-mRNA 相互作用网络显示,在 CFA 5d 组中,miR-124、miR-149、miR-3584 及其靶基因 IL-6R、ADAM19、LAMC1 和 CERS2 的表达发生了显著变化。在 CFA 14d 组中,miR-124、miR-29、miR-34、miR-30、miR-338 和其靶基因 TIMP2、CREB5 和 EFNB1 也发生了显著变化。我们还研究了一个相互作用对,miR-124-3p 和 IL-6R,结果表明 miR-124-3p 可以减轻炎症性疼痛并降低脊髓中的 IL-6R 表达。这些特定的 miRNA 和它们的靶基因为炎症性疼痛的诊断和治疗提供了可能的途径。