Role of microRNA-155 in autoimmunity

被引:167
作者
Leng, Rui-Xue [1 ]
Pan, Hai-Feng [1 ]
Qin, Wei-Zi [1 ]
Chen, Gui-Mei [1 ]
Ye, Dong-Qing [1 ]
机构
[1] Anhui Med Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, Hefei 230032, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
MicroRNA-155; Immune cells; Autoimmune diseases; SYSTEMIC-LUPUS-ERYTHEMATOSUS; REGULATORY T-CELLS; RHEUMATOID-ARTHRITIS PATIENTS; INOSITOL PHOSPHATASE SHIP; MULTIPLE-SCLEROSIS; NEGATIVE REGULATOR; DENDRITIC CELLS; HIGH EXPRESSION; NONCODING RNA; MIR-155;
D O I
10.1016/j.cytogfr.2011.05.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
MicroRNAs (miRNAs) have recently emerged as a major class of gene expression regulators linked to most biological functions. MiR-155 is encoded within a region known as B cell integration cluster (Bic) gene, identified originally as a frequent integration site for the avian leukosis virus. Disregulation of endogenous miR-155 has been implicated in the pathogenesis of human cancers. Recently, aberrant expression of miR-155 was observed in many autoimmune conditions, including rheumatoid arthritis (RA), multiple sclerosis (MS), and systemic lupus erythematosus (SLE). Moreover, functional analysis demonstrated that miR-155 has powerful regulatory potential in a wide variety of immune cells through targeting specific mRNAs. Since pathogenic immune cells play a pivotal role in pathogenesis of human autoimmune diseases, miR-155 might be a versatile therapeutic target. This review will discuss the current understandings for the role of miR-155 in autoimmunity. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:141 / 147
页数:7
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