Expression of T cell-related lncRNAs in multiple sclerosis

被引:9
作者
Dadyar, Maryam [1 ]
Hussen, Bashdar Mahmud [2 ,3 ]
Eslami, Solat [4 ,5 ]
Taheri, Mohammad [6 ]
Emadi, Farhad [7 ]
Ghafouri-Fard, Soudeh [1 ]
Sayad, Arezou [1 ]
机构
[1] Shahid Beheshti Univ Med Sci, Sch Med, Dept Med Genet, Tehran, Iran
[2] Hawler Med Univ, Coll Pharm, Dept Pharmacognosy, Erbil, Kurdistan Regio, Iraq
[3] Lebanese French Univ, Ctr Res Strateg Studies, Erbil, Kurdistan Regio, Iraq
[4] Alborz Univ Med Sci, Sch Med, Dept Med Biotechnol, Karaj, Iran
[5] Alborz Univ Med Sci, Dietary Supplements & Probiot Res Ctr, Karaj, Iran
[6] Jena Univ Hosp, Inst Human Genet, Jena, Germany
[7] Shahid Beheshti Univ Med Sci, Skull Base Res Ctr, Tehran, Iran
关键词
FLICR; NEST; RMRP; TH2-LCR; lncRNA; multiple sclerosis; T cell; FOXP3; EXPRESSION; SUSCEPTIBILITY; SUPPRESSION;
D O I
10.3389/fgene.2022.967157
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Long non-coding RNAs (lncRNAs) have been demonstrated to in the pathophysiology of multiple sclerosis (MS). In order to appraise the role of T cell-related lncRNAs in this disorder, we assessed expressions of NEST, RMRP, TH2-LCR, MAFTRR and FLICR in MS patients and healthy individuals. We detected significant difference in the expression of RMRP and FLICR between cases and controls. There were substantial correlations between expressions of NEST, RMRP, TH2-LCR, MAFTRR and FLICR lncRNAs among patients, but not controls. The strongest correlations were found between RMRP and TH2-LCR, and between MAFTRR and RMRP with correlation coefficients of 0.69 and 0.59, respectively. ROC curve analysis revealed appropriate power of FLICR in differentiating between MS patients and healthy controls (AUC value = 0.84). Expression of NEST lncRNA was positively correlated with disease duration in MS patients, but negatively correlated with age at onset. In brief, we reported dysregulation of two T cell-related lncRNAs in MS patients and proposed FLICR as a putative marker for this disorder.
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页数:7
相关论文
共 23 条
[1]   Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 [J].
Bahlo, Melanie ;
Booth, David R. ;
Broadley, Simon A. ;
Brown, Matthew A. ;
Foote, Simon J. ;
Griffiths, Lyn R. ;
Kilpatrick, Trevor J. ;
Lechner-Scott, Jeanette ;
Moscato, Pablo ;
Perreau, Victoria M. ;
Rubio, Justin P. ;
Scott, Rodney J. ;
Stankovich, Jim ;
Stewart, Graeme J. ;
Taylor, Bruce V. ;
Wiley, James ;
Clarke, Glynnis ;
Cox, Mathew B. ;
Csurhes, Peter A. ;
Danoy, Patrick ;
Drysdale, Karen ;
Field, Judith ;
Foote, Simon J. ;
Greer, Judith M. ;
Guru, Preethi ;
Hadler, Johanna ;
McMorran, Brendan J. ;
Jensen, Cathy J. ;
Johnson, Laura J. ;
McCallum, Ruth ;
Merriman, Marilyn ;
Merriman, Tony ;
Pryce, Karen ;
Tajouri, Lotfi ;
Wilkins, Ella J. ;
Browning, Brian L. ;
Browning, Sharon R. ;
Perera, Devindri ;
Butzkueven, Helmut ;
Carroll, William M. ;
Chapman, Caron ;
Kermode, Allan G. ;
Marriott, Mark ;
Mason, Deborah ;
Heard, Robert N. ;
Pender, Michael P. ;
Slee, Mark ;
Tubridy, Niall ;
Willoughby, Ernest .
NATURE GENETICS, 2009, 41 (07) :824-U84
[2]   Regulatory T cells fail to suppress CD4+ T-bet+ T cells in relapsing multiple sclerosis patients [J].
Frisullo, Giovanni ;
Nociti, Viviana ;
Iorio, Raffaele ;
Patanella, Agata K. ;
Caggiula, Marcella ;
Marti, Alessandro ;
Sancricca, Cristina ;
Angelucci, Francesco ;
Mirabella, Massimiliano ;
Tonali, Pietro A. ;
Batocchi, Anna P. .
IMMUNOLOGY, 2009, 127 (03) :418-428
[3]   Intracerebral Human Regulatory T Cells: Analysis of CD4+CD25+FOXP3+ T Cells in Brain Lesions and Cerebrospinal Fluid of Multiple Sclerosis Patients [J].
Fritzsching, Benedikt ;
Haas, Juergen ;
Koenig, Fatima ;
Kunz, Pierre ;
Fritzsching, Eva ;
Poeschl, Johannes ;
Krammer, Peter H. ;
Brueck, Wolfgang ;
Suri-Payer, Elisabeth ;
Wildemann, Brigitte .
PLOS ONE, 2011, 6 (03)
[4]   A comprehensive review of non-coding RNAs functions in multiple sclerosis [J].
Ghafouri-Fard, Soudeh ;
Taheri, Mohammad .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2020, 879
[5]   The NeST Long ncRNA Controls Microbial Susceptibility and Epigenetic Activation of the Interferon-γ Locus [J].
Gomez, J. Antonio ;
Wapinski, Orly L. ;
Yang, Yul W. ;
Bureau, Jean-Francois ;
Gopinath, Smita ;
Monack, Denise M. ;
Chang, Howard Y. ;
Brahic, Michel ;
Kirkegaard, Karla .
CELL, 2013, 152 (04) :743-754
[6]   Reduced suppressive effect of CD4+CD25high regulatory T cells on the T cell immune response against myelin oligodendrocyte glycoprotein in patients with multiple sclerosis [J].
Haas, J ;
Hug, A ;
Viehöver, A ;
Fritzsching, B ;
Falk, CS ;
Filser, A ;
Vetter, T ;
Milkova, L ;
Korporal, M ;
Fritz, B ;
Storch-Hagenlocher, B ;
Krammer, PH ;
Suri-Payer, E ;
Wildemann, B .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2005, 35 (11) :3343-3352
[7]   Long Non-Coding RNAs, Novel Offenders or Guardians in Multiple Sclerosis: A Scoping Review [J].
Jalaiei, Abbas ;
Asadi, Mohammad Reza ;
Sabaie, Hani ;
Dehghani, Hossein ;
Gharesouran, Jalal ;
Hussen, Bashdar Mahmud ;
Taheri, Mohammad ;
Ghafouri-Fard, Soudeh ;
Rezazadeh, Maryam .
FRONTIERS IN IMMUNOLOGY, 2021, 12
[8]  
Kimura K., 2020, CLIN EXP NEUROIMMUNO, V11, P148, DOI [10.1111/cen3.12591, DOI 10.1111/CEN3.12591]
[9]   T Regulatory Cells Are Markers of Disease Activity in Multiple Sclerosis Patients [J].
Libera, Dacia Dalla ;
Di Mitri, Diletta ;
Bergami, Alessandra ;
Centonze, Diego ;
Gasperini, Claudio ;
Grasso, Maria Grazia ;
Galgani, Simona ;
Martinelli, Vittorio ;
Comi, Giancarlo ;
Avolio, Carlo ;
Martino, Gianvito ;
Borsellino, Giovanna ;
Sallusto, Federica ;
Battistini, Luca ;
Furlan, Roberto .
PLOS ONE, 2011, 6 (06)
[10]   TH1 AND TH2 CD4(+) T-CELLS IN THE PATHOGENESIS OF ORGAN-SPECIFIC AUTOIMMUNE-DISEASES [J].
LIBLAU, RS ;
SINGER, SM ;
MCDEVITT, HO .
IMMUNOLOGY TODAY, 1995, 16 (01) :34-38