miR-155: an ancient regulator of the immune system

被引:255
作者
Vigorito, Elena [1 ]
Kohlhaas, Susan [1 ]
Lu, Dong [1 ]
Leyland, Rebecca [1 ]
机构
[1] Babraham Inst, Lab Lymphocyte Signalling & Dev, Cambridge CB22 3AT, England
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
miR-155; miRNAs; immune system; B cells; therapeutics; INDUCED CYTIDINE DEAMINASE; B-CELL LYMPHOMAS; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; VIRUS-INDUCED LYMPHOMAS; PEPTIDE NUCLEIC-ACIDS; T-CELL; SALMONELLA-TYPHIMURIUM; IFN-GAMMA; DENDRITIC CELLS; MESSENGER-RNAS;
D O I
10.1111/imr.12057
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
MicroRNAs (miRNAs) are a newly recognized class of regulatory genes which repress the expression of protein-coding genes. Numerous studies have uncovered a complex role for miRNAs regulating many aspects of a variety of cellular processes including cell growth, differentiation, and lineage commitment. In the immune system, miR-155 is unique in its ability to shape the transcriptome of activated myeloid and lymphoid cells controlling diverse biological functions ranging from inflammation to immunological memory. Not surprisingly, a tight control of miR-155 expression is required to avoid malignant transformation, as evidenced by miR-155 overexpression in many cancers of B-cell origin. In this review, we discuss the potential of miR-155 as a molecular target for therapeutic intervention and discuss the function of miR-155 in the context of protective immunity. We first look back into the emergence of miR-155 in evolution, which is coincidental with the emergence of the ancestors of the antigen receptors. We then summarize what we have learned about the role of miR-155 in the regulation of lymphoid subsets at the cellular and molecular level in the context of recent progress in this field.
引用
收藏
页码:146 / 157
页数:12
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