首页 | 本学科首页   官方微博 | 高级检索  
     


Expression and genetic analysis of miRNAs involved in CD4+ cell activation in patients with multiple sclerosis
Authors:Fenoglio Chiara  Cantoni Claudia  De Riz Milena  Ridolfi Elisa  Cortini Francesca  Serpente Maria  Villa Chiara  Comi Cristoforo  Monaco Francesco  Mellesi Luisa  Valzelli Stefano  Bresolin Nereo  Galimberti Daniela  Scarpini Elio
Affiliation:a Department of Neurological Sciences, “Dino Ferrari” Center, University of Milan, Fondazione Cà Granda, IRCCS Ospedale Maggiore Policlinico, Milan, Italy
b Department of Neurology, Ospedale Maggiore, Novara, Italy
c Department of Neurology and Interdisciplinary Research Centre of Autoimmune Diseases (IRCAD), Amedeo Avogadro University, Novara, Italy
d Neurorehabilitation Institute, M.L. Novarese, Moncrivello (VC), Italy
e Bayer ScheringPharma, Italy
Abstract:MicroRNA (miRNA)-mediate RNA interference has been identified as a novel mechanism that regulates protein expression. It is recognised that miRNAs play essential roles in the immune system and for correct function in the brain. Moreover, it is now clear that abnormal miRNA expression is a common feature of several diseases involving the immune system including multiple sclerosis (MS). Expression analysis for miR-21, miR-146a and -b, miR-150, miR-155 was carried out in peripheral mononuclear cells (PBMC) from a cohort of 29 MS patients and 19 controls. Subsequently, a case control study for miR-146 rs2910164 variant was performed in an overall population of 346 MS cases and 339 controls. A statistically significant increased expression of miR-21, miR-146a and -b was observed in relapsing remitting (RR)MS patients as compared with controls (1.44 ± 0.13 vs 0.79 ± 0.06, P = 0.036; 1.50 ± 0.12 vs 0.84 ± 0.08, P = 0.039; 1.54 ± 0.15 vs 0.72 ± 0.08, P = 0.001 respectively). On the contrary, no differences were found in the expression levels of both miR-150 and miR-155 in patients as compared with controls (P > 0.05). The genetic association study failed to find any differences in the frequencies of rs2910164 between patients and controls. miRNA dysregulation may contribute to the pathogenesis of MS and highlights the possibility to define different disease entities with specific miRNAs profile.
Keywords:CD4+   Multiple sclerosis   Risk factor   Immune system   miRNA   Gene expression
本文献已被 ScienceDirect PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号