Department of Neurobiology and Anatomy, Drexel University College of Medicine Philadelphia, PA, USA.
Front Mol Neurosci. 2013 Oct 24;6:35. doi: 10.3389/fnmol.2013.00035. eCollection 2013.
MicroRNAs (miRNAs) are small, non-coding RNAs that function as key post-transcriptional regulators in neural development, brain function, and neurological diseases. Growing evidence indicates that miRNAs are also important mediators of nerve regeneration, however, the affected signaling mechanisms are not clearly understood. In the present study, we show that nerve injury-induced miR-431 stimulates regenerative axon growth by silencing Kremen1, an antagonist of Wnt/beta-catenin signaling. Both the gain-of-function of miR-431 and knockdown of Kremen1 significantly enhance axon outgrowth in murine dorsal root ganglion neuronal cultures. Using cross-linking with AGO-2 immunoprecipitation, and 3'-untranslated region (UTR) luciferase reporter assay we demonstrate miR-431 direct interaction on the 3'-UTR of Kremen1 mRNA. Together, our results identify miR-431 as an important regulator of axonal regeneration and a promising therapeutic target.
微小 RNA(miRNAs)是小的非编码 RNA,作为神经发育、大脑功能和神经疾病的关键转录后调节剂发挥作用。越来越多的证据表明,miRNAs 也是神经再生的重要介质,然而,受影响的信号机制尚不清楚。在本研究中,我们表明,神经损伤诱导的 miR-431 通过沉默 Wnt/β-连环蛋白信号的拮抗剂 Kremen1 来刺激再生轴突的生长。miR-431 的功能获得和 Kremen1 的敲低均显著增强了鼠背根神经节神经元培养物中的轴突生长。通过 AGO-2 免疫沉淀交联和 3'非翻译区(UTR)荧光素酶报告基因测定,我们证明了 miR-431 对 Kremen1 mRNA 的 3'UTR 的直接作用。总之,我们的结果表明 miR-431 是轴突再生的重要调节因子,也是有前途的治疗靶点。