Small RNA Regulators of T Cell-Mediated Autoimmunity

被引:22
作者
Jeker, Lukas T. [1 ,2 ]
Bluestone, Jeffrey A. [1 ]
机构
[1] Univ Calif San Francisco, Ctr Diabet, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
基金
瑞士国家科学基金会;
关键词
MicroRNA; autoimmunity; dicer; immune homeostasis; regulatory T cells (Treg); GENE-EXPRESSION; MICRORNA BIOGENESIS; AFFINITY THRESHOLD; THYMIC SELECTION; FOXP3; EXPRESSION; MESSENGER-RNAS; LINEAGE CHOICE; SIRNA DELIVERY; ENZYME DICER; DIFFERENTIATION;
D O I
10.1007/s10875-010-9392-7
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 short single-stranded RNA molecules that regulate gene expression post-transcriptionally. Several hundred miRNAs exist in the mammalian genome and regulate developmental processes, cell cycle, and survival. In this review, we highlight general modes of miRNA function and relate them to how such regulation can be beneficial for immune homeostasis and the prevention of autoimmune diseases. We highlight examples of experimentally verified miRNA function and their target genes in the immune system and place them in context of concepts relevant to an understanding of autoimmune pathogenesis. Where available, we refer to clinical correlations. Finally, we speculate how emerging knowledge about miRNA function in the immune system might be used diagnostically and therapeutically.
引用
收藏
页码:347 / 357
页数:11
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