作者
Riccardo L Rossi, Grazisa Rossetti, Lynn Wenandy, Serena Curti, Anna Ripamonti, Raoul JP Bonnal, Roberto Sciarretta Birolo, Monica Moro, Maria C Crosti, Paola Gruarin, Stefano Maglie, Francesco Marabita, Debora Mascheroni, Valeria Parente, Mario Comelli, Emilio Trabucchi, Raffaele De Francesco, Jens Geginat, Sergio Abrignani, Massimiliano Pagani
发表日期
2011/8
期刊
Nature immunology
卷号
12
期号
8
页码范围
796-803
出版商
Nature Publishing Group US
简介
MicroRNAs are small noncoding RNAs that regulate gene expression post-transcriptionally. Here we applied microRNA profiling to 17 human lymphocyte subsets to identify microRNA signatures that were distinct among various subsets and different from those of mouse lymphocytes. One of the signature microRNAs of naive CD4+ T cells, miR-125b, regulated the expression of genes encoding molecules involved in T cell differentiation, including IFNG, IL2RB, IL10RA and PRDM1. The expression of synthetic miR-125b and lentiviral vectors encoding the precursor to miR-125b in naive lymphocytes inhibited differentiation to effector cells. Our data provide an 'atlas' of microRNA expression in human lymphocytes, define subset-specific signatures and their target genes and indicate that the naive state of T cells is enforced by microRNA.
引用总数
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