Caggiu Elisa, Paulus Kai, Mameli Giuseppe, Arru Giannina, Sechi Gian Pietro, Sechi Leonardo A
Department of Biomedical Sciences, Section of Microbiology and Virology, University of Sassari, Viale San Pietro 43b, 07100 Sassari, Italy.
UOC Neurologia, Azienda-Ospedaliero Universitaria di Sassari, Italy.
eNeurologicalSci. 2018 Sep 14;13:1-4. doi: 10.1016/j.ensci.2018.09.002. eCollection 2018 Dec.
Parkinson's disease is a neurodegenerative disorder and its etiology is unknown, numerous studies show how different environmental factors can influence the development of disease. miRNAs are involved in several pathologies and their dysregulation contribute to different pathologies, also in neurodegenerative such as Parkinson's disease, Alzheimer's disease, Huntington's disease and Amyotrophic lateral sclerosis. In this study, we profiled the expression of different candidate miRNAs: miR-155, miR-26a, miR-146a, and miR132, in PBMCs of L-dopa treated Parkinson patients and unaffected controls (HCs).We investigated the expression of miRNAs by RT-real time PCR, the results were subjected to statistical analysis. miRNA-155-5p was generally up-regulated in PD patients compared to HCs whereas miRNA-146a-5p was down-regulated in PD patients in comparison to HCs. It is interesting to point out that the expression of miR-155-5p was modified by levodopa treatment, in fact a down-regulation of miR-155-5p in PD patients with the highest dosage was observed. In conclusion, miRNA 155 could not only be a promising target for the anti-inflammatory therapy in PD but also a good candidate as a disease progression biomarker. The role of levodopa in modulating the levels of miRNA 155 requires further studies.
帕金森病是一种神经退行性疾病,其病因尚不清楚,众多研究表明不同环境因素如何影响该疾病的发展。微小RNA(miRNA)参与多种病理过程,其失调也会导致不同的病理状况,在神经退行性疾病如帕金森病、阿尔茨海默病、亨廷顿病和肌萎缩侧索硬化症中亦是如此。在本研究中,我们分析了不同候选miRNA:miR-155、miR-26a、miR-146a和miR-132在接受左旋多巴治疗的帕金森病患者及未受影响的对照者(健康对照)外周血单核细胞(PBMC)中的表达情况。我们通过逆转录实时定量聚合酶链反应(RT-实时PCR)研究了miRNA的表达,并对结果进行了统计分析。与健康对照相比,帕金森病患者中miRNA-155-5p总体上调,而miRNA-146a-5p在帕金森病患者中下调。值得指出的是,左旋多巴治疗改变了miR-155-5p的表达,事实上,在服用最高剂量左旋多巴的帕金森病患者中观察到miR-155-5p下调。总之,miRNA 155不仅可能是帕金森病抗炎治疗的一个有前景的靶点,也是疾病进展生物标志物的一个良好候选者。左旋多巴在调节miRNA 155水平方面的作用需要进一步研究。