microRNAs and the immune response

被引:625
作者
Tsitsiou, Eleni [1 ]
Lindsay, Mark A. [1 ]
机构
[1] Univ Manchester, Wythenshawe Hosp, NIHR Resp Translat Res Facil, Manchester M23 9LT, Lancs, England
基金
英国惠康基金;
关键词
INDUCED CYTIDINE DEAMINASE; REGULATORY T-CELLS; INFLAMMATORY RESPONSE; RAPID CHANGES; EXPRESSION; DICER; DIFFERENTIATION; LINEAGE; AUTOIMMUNITY; BIOGENESIS;
D O I
10.1016/j.coph.2009.05.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although the immune response is predominantly controlled at the transcriptional level, microRNA-mediated RNA interference is emerging as an important regulatory mechanism that operates at the translation level. Specifically, recent studies indicate that those miRNAs that are selectively and/or highly expressed in immune cells including the miR-17-92 cluster, miR-150, miR-155, miR-181 and miR-223 have a 'permissive' function in the maturation, proliferation and differentiation of myeloid and lymphoid cells. Importantly, these actions of miRNAs often involve interactions with transcription factors. In contrast, the rapid and transient induction of miR-9, miR-146a and miR-155 has been speculated to negatively regulate the acute responses following activation of innate immune through down-regulation of proteins involved in the receptor-induced signalling pathways.
引用
收藏
页码:514 / 520
页数:7
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