Expression and genetic analysis of miRNAs involved in CD4+cell activation in patients with multiple sclerosis

被引:150
作者
Fenoglio, Chiara [1 ]
Cantoni, Claudia [1 ]
De Riz, Milena [1 ]
Ridolfi, Elisa [1 ]
Cortini, Francesca [1 ]
Serpente, Maria [1 ]
Villa, Chiara [1 ]
Comi, Cristoforo [2 ,3 ,4 ,5 ]
Monaco, Francesco [2 ,3 ,4 ]
Mellesi, Luisa
Valzelli, Stefano
Bresolin, Nereo [1 ]
Galimberti, Daniela [1 ]
Scarpini, Elio [1 ]
机构
[1] Univ Milan, Dept Neurol Sci, Dino Ferrari Ctr, Fdn Ca Granda,IRCCS Osped Maggiore Policlin, Milan, Italy
[2] Osped Maggiore Novara, Dept Neurol, Novara, Italy
[3] Amedeo Avogadro Univ, Dept Neurol, Novara, Italy
[4] Amedeo Avogadro Univ, IRCAD, Novara, Italy
[5] ML Novarese, Neurorehabil Inst, Moncrivello, VC, Italy
关键词
CD4+; Multiple sclerosis; Risk factor; Immune system; miRNA; Gene expression; IMMUNE-RESPONSE; AUTOIMMUNE-DISEASES; MICRORNAS; DIFFERENTIATION; PATHOGENESIS; INFLAMMATION; REGULATORS; MIR-150; SYSTEM;
D O I
10.1016/j.neulet.2011.08.021
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:9 / 12
页数:4
相关论文
共 32 条
[1]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[2]   MicroRNAs: Novel Regulators During the Immune Response [J].
Bi, Yujing ;
Liu, Guangwei ;
Yang, Ruifu .
JOURNAL OF CELLULAR PHYSIOLOGY, 2009, 218 (03) :467-472
[3]   A role for Dicer in immune regulation [J].
Cobb, Bradley S. ;
Hertweck, Arnulf ;
Smith, James ;
O'Connor, Eric ;
Graf, Daniel ;
Cook, Terence ;
Smale, Stephen T. ;
Sakaguchi, Shimon ;
Livesey, Frederick J. ;
Fisher, Amanda G. ;
Merkenschlager, Matthias .
JOURNAL OF EXPERIMENTAL MEDICINE, 2006, 203 (11) :2519-2527
[4]  
Cox MB, 2010, PLOS ONE, V5, DOI [10.1371/journal.pone.0012132, 10.1371/journal.pone.0011044]
[5]   MicroRNA, a new paradigm for understanding immunoregulation, inflammation, and autoimmune diseases [J].
Dai, Rujuan ;
Ahmed, S. Ansar .
TRANSLATIONAL RESEARCH, 2011, 157 (04) :163-179
[6]   Altered miRNA expression in T regulatory cells in course of multiple sclerosis [J].
De Santis, Giuseppe ;
Ferracin, Manuela ;
Biondani, Andrea ;
Caniatti, Luisa ;
Tola, Maria Rosaria ;
Castellazzi, Massimiliano ;
Zagatti, Barbara ;
Battistini, Luca ;
Borsellino, Giovanna ;
Fainardi, Enrico ;
Gavioli, Riccardo ;
Negrini, Massimo ;
Furlan, Roberto ;
Granieri, Enrico .
JOURNAL OF NEUROIMMUNOLOGY, 2010, 226 (1-2) :165-171
[7]   MicroRNA miR-326 regulates TH-17 differentiation and is associated with the pathogenesis of multiple sclerosis [J].
Du, Changsheng ;
Liu, Chang ;
Kang, Jiuhong ;
Zhao, Guixian ;
Ye, Zhiqiang ;
Huang, Shichao ;
Li, Zhenxin ;
Wu, Zhiying ;
Pei, Gang .
NATURE IMMUNOLOGY, 2009, 10 (12) :1252-U4
[8]   Single nucleotide polymorphism associated with mature miR-125a alters the processing of pri-miRNA [J].
Duan, Ranhui ;
Pak, ChangHui ;
Jin, Peng .
HUMAN MOLECULAR GENETICS, 2007, 16 (09) :1124-1131
[9]   miR-155 gene: A typical multifunctional microRNA [J].
Faraoni, Isabella ;
Antonetti, Francesca Romana ;
Cardone, John ;
Bonmassar, Enzo .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2009, 1792 (06) :497-505
[10]   Progranulin gene variability increases the risk for primary progressive multiple sclerosis in males [J].
Fenoglio, C. ;
Scalabrini, D. ;
Esposito, F. ;
Comi, C. ;
Cavalla, P. ;
De Riz, M. ;
Martinelli, V. ;
Piccio, L. M. ;
Venturelli, E. ;
Fumagalli, G. ;
Capra, R. ;
Collimedaglia, L. ;
Ghezzi, A. ;
Rodegher, M. E. ;
Vercellino, M. ;
Leone, M. ;
Giordana, M. T. ;
Bresolin, N. ;
Monaco, F. ;
Comi, G. ;
Scarpini, E. ;
Martinelli-Boneschi, F. ;
Galimberti, D. .
GENES AND IMMUNITY, 2010, 11 (06) :497-503