Neumann Elena, Hermanns Henning, Barthel Franziska, Werdehausen Robert, Brandenburger Timo
Department of Anesthesiology, Medical Faculty, Heinrich-Heine-University Düsseldorf, Moorenstr. 5, 40225, Düsseldorf, Germany.
Department of Anesthesiology, Academic Medical Center, Meibergdreef 9, 1100 DD, Amsterdam, The Netherlands.
Mol Pain. 2015 Jun 26;11:39. doi: 10.1186/s12990-015-0045-y.
MicroRNAs (miRNAs) are involved in the neuroplastic changes which induce and maintain neuropathic pain. However, it is unknown whether nerve injury leads to altered miRNA expression and modulation of pain relevant target gene expression within peripheral nerves. In the present study, expression profiles of miR-1 and the pain-relevant targets, brain derived neurotrophic factor (BDNF) and Connexin 43 (Cx43), were studied in peripheral neuropathic pain, which was induced by chronic constriction injury (CCI) of the sciatic nerve in rats. The expression of miR-1 was investigated in the sciatic nerve, dorsal root ganglion (DRG) and the ipsilateral spinal cord by qPCR. Changes of BDNF and Cx43 expression patterns were studied using qPCR, Western blot analysis, ELISA and immunohistochemistry.
In sciatic nerves of naïve rats, expression levels of miR-1 were more than twice as high as in DRG and spinal cord. In neuropathic rats, CCI lead to a time-dependent downregulation of miR-1 in the sciatic nerve but not in DRG and spinal cord. Likewise, protein expression of the miR-1 targets BDNF and Cx43 was upregulated in the sciatic nerve and DRG after CCI. Immunohistochemical staining revealed an endoneural abundancy of Cx43 in injured sciatic nerves which was absent after Sham operation.
This study demonstrates that CCI leads to a regulation of miRNAs (miR-1) in the peripheral nervous system. This regulation is associated with alterations in the expression and localization of the miR-1 dependent pain-relevant proteins BDNF and Cx43. Further studies will have to explore the function of miRNAs in the context of neuropathic pain in the peripheral nervous system.
微小RNA(miRNA)参与诱导和维持神经性疼痛的神经可塑性变化。然而,神经损伤是否会导致外周神经内miRNA表达改变以及疼痛相关靶基因表达的调节尚不清楚。在本研究中,我们研究了miR-1以及疼痛相关靶点脑源性神经营养因子(BDNF)和连接蛋白43(Cx43)在大鼠坐骨神经慢性压迫损伤(CCI)诱导的外周神经性疼痛中的表达谱。通过qPCR检测坐骨神经、背根神经节(DRG)和同侧脊髓中miR-1的表达。使用qPCR、蛋白质免疫印迹分析、酶联免疫吸附测定(ELISA)和免疫组织化学研究BDNF和Cx43表达模式的变化。
在未处理大鼠的坐骨神经中,miR-1的表达水平比DRG和脊髓中的高两倍以上。在神经性疼痛大鼠中,CCI导致坐骨神经中miR-1随时间依赖性下调,但在DRG和脊髓中未出现这种情况。同样,CCI后坐骨神经和DRG中miR-1靶点BDNF和Cx43的蛋白质表达上调。免疫组织化学染色显示,损伤的坐骨神经中有丰富的神经内膜Cx43,假手术组则没有。
本研究表明,CCI导致外周神经系统中miRNA(miR-1)的调节。这种调节与miR-1依赖性疼痛相关蛋白BDNF和Cx43的表达及定位改变有关。进一步的研究将不得不探索miRNA在周围神经系统神经性疼痛背景下的功能。