MicroRNA regulation of lymphocyte tolerance and autoimmunity

被引:120
作者
Simpson, Laura J. [1 ]
Ansel, K. Mark [1 ]
机构
[1] Univ Calif San Francisco, Dept Microbiol & Immunol, Sandler Asthma Basic Res Ctr, San Francisco, CA 94143 USA
基金
美国国家科学基金会;
关键词
CD4(+) T-CELLS; MULTIPLE-SCLEROSIS; CUTTING EDGE; B-CELLS; MIR-17-SIMILAR-TO-92; FAMILY; TH17; DIFFERENTIATION; MEDIATED REGULATION; NEGATIVE REGULATION; MIRNA EXPRESSION; FOXP3; EXPRESSION;
D O I
10.1172/JCI78090
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Understanding the cell-intrinsic cues that permit self-reactivity in lymphocytes, and therefore autoimmunity, requires an understanding of the transcriptional and posttranscriptional regulation of gene expression in these cells. In this Review, we address seminal and recent research on microRNA (mIRNA) regulation of central and peripheral tolerance. Human and mouse studies demonstrate that the PI3K pathway is a critical point of miRNA regulation of immune cell development and function that affects the development of autoimmunity. We also discuss how miRNA expression profiling in human autoimmune diseases has inspired mechanistic studies of miRNA function in the pathogenesis of multiple sclerosis, rheumatoid arthritis, systemic lupus erythematosus, type 1 diabetes, and asthma.
引用
收藏
页码:2242 / 2249
页数:8
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