MicroRNA-146a in autoimmunity and innate immune responses

被引:82
作者
Chan, Edward K. L. [1 ,2 ]
Ceribelli, Angela [1 ]
Satoh, Minoru [3 ,4 ]
机构
[1] Univ Florida, Dept Oral Biol, Gainesville, FL 32610 USA
[2] Univ Florida, Dept Anat & Cell Biol, Gainesville, FL 32610 USA
[3] Univ Florida, Dept Med, Div Rheumatol & Clin Immunol, Gainesville, FL 32610 USA
[4] Univ Florida, Dept Pathol Immunol & Lab Med, Gainesville, FL 32610 USA
基金
美国国家卫生研究院;
关键词
TUMOR-NECROSIS-FACTOR; RHEUMATOID-ARTHRITIS PATIENTS; MESSENGER-RNA DECAY; NF-KAPPA-B; GW BODIES; IN-VIVO; ENDOTOXIN TOLERANCE; MIR-146A EXPRESSION; MEDIATED REGULATION; MONONUCLEAR-CELLS;
D O I
10.1136/annrheumdis-2012-202203
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
MicroRNA (miRNA) are approximately 22 nucleotide single-stranded RNA that regulate the stability of target messenger RNA by selective binding to specific sites at the 3'-untranslated regions (UTR). This triggers repression in translation and mRNA degradation. It has been estimated that approximately 60% of all mRNA are under the control of miRNA. Among the known hundreds of miRNA, some are considered master regulators controlling either a single or multiple cellular pathways. Some miRNA are known to affect development and cell differentiation, while others are implicated in immunity and autoimmune diseases. A very interesting example is miR-146a, which has been reported to be downregulated in systemic lupus erythematosus and upregulated in rheumatoid arthritis (RA). Several groups have recently focused their attention on miRNA in the pathogenesis of RA. Interestingly, the expression of miR-146a is upregulated in different cell types and tissues in RA patients. miRNA in RA could also be considered as possible future targets for new therapeutic approaches. This discussion will focus on the current understanding in the function of miR-146a in endotoxin tolerance and cross-tolerance, and how it may contribute to modulate the overproduction of known pathogenic cytokines, such as tumour necrosis factor alpha.
引用
收藏
页码:90 / 95
页数:6
相关论文
共 64 条
[1]
MicroRNA 146a Expression in Rheumatoid Arthritis: Association with Tumor Necrosis Factor-Alpha and Disease Activity [J].
Abou-Zeid, Abla ;
Saad, Mowaffak ;
Soliman, Eiman .
GENETIC TESTING AND MOLECULAR BIOMARKERS, 2011, 15 (11) :807-812
[2]
Compensatory anti-inflammatory response syndrome [J].
Adib-Conquy, Minou ;
Cavaillon, Jean-Marc .
THROMBOSIS AND HAEMOSTASIS, 2009, 101 (01) :36-47
[4]
SHIP, TGF-β, and endotoxin tolerance [J].
Beutler, B .
IMMUNITY, 2004, 21 (02) :134-135
[5]
BEUTLER B, 1987, NEW ENGL J MED, V316, P379
[6]
Clinical and serological features of patients with autoantibodies to GW/P bodies [J].
Bhanji, Rahima A. ;
Eystathioy, Theophany ;
Chan, Edward K. L. ;
Bloch, Donald B. ;
Fritzler, Marvin J. .
CLINICAL IMMUNOLOGY, 2007, 125 (03) :247-256
[7]
Role for MyD88-independent, TRIF pathway in lipid A TLR4-induced endotoxin tolerance [J].
Biswas, Subhra K. ;
Bist, Pradeep ;
Dhillon, Manprit Kaur ;
Kajiji, Tasneem ;
del Fresno, Carlos ;
Yamamoto, Masahiro ;
Lopez-Collazo, Eduardo ;
Akira, Shizuo ;
Tergaonkar, Vinay .
JOURNAL OF IMMUNOLOGY, 2007, 179 (06) :4083-4092
[8]
miR-146a is a significant brake on autoimmunity, myeloproliferation, and cancer in mice [J].
Boldin, Mark P. ;
Taganov, Konstantin D. ;
Rao, Dinesh S. ;
Yang, Lili ;
Zhao, Jimmy L. ;
Kalwani, Manorama ;
Garcia-Flores, Yvette ;
Luong, Mui ;
Devrekanli, Asli ;
Xu, Jessica ;
Sun, Guizhen ;
Tay, Jia ;
Linsley, Peter S. ;
Baltimore, David .
JOURNAL OF EXPERIMENTAL MEDICINE, 2011, 208 (06) :1189-1201
[9]
Human TLRs and IL-1Rs in Host Defense: Natural Insights from Evolutionary, Epidemiological, and Clinical Genetics [J].
Casanova, Jean-Laurent ;
Abel, Laurent ;
Quintana-Murci, Lluis .
ANNUAL REVIEW OF IMMUNOLOGY, VOL 29, 2011, 29 :447-491
[10]
Contrast in Aberrant MicroRNA Expression in Systemic Lupus Erythematosus and Rheumatoid Arthritis: Is MicroRNA-146 All We Need? [J].
Chan, Edward K. L. ;
Satoh, Minoru ;
Pauley, Kaleb M. .
ARTHRITIS AND RHEUMATISM, 2009, 60 (04) :912-915