<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>Molecular Immunology, MR, NIMR</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA259433</full_dataset_link><scientific_name>Mus musculus</scientific_name><tag>xref:PubMed:25035954</tag><long_description>Foxp3+ regulatory T (Treg) cells prevent inflammatory disease but the mechanistic basis of suppression is not understood completely . Gene silencing by RNA interference can act in a cell-autonomous and non-cell-autonomous manner, providing mechanisms of inter-cellular regulation. Here, we demonstrate that non-cell-autonomous gene silencing, mediated by miRNA-containing exosomes, is a mechanism employed by Treg cells to suppress T cell-mediated disease. Treg cells transferred microRNAs (miRNA) to various immune cells, including T helper 1 (Th1) cells, suppressing Th1 cell proliferation and cytokine secretion. Use of Dicer-deficient or Rab27a and Rab27b double-deficient Treg cells to disrupt miRNA-biogenesis or the exosomal pathway, respectively, established a requirement for miRNAs and exosomes for Treg cell-mediated suppression. Transcriptional analysis and miRNA inhibitor studies showed that exosome-mediated transfer of Let-7d from Treg cell to Th1 cells contributed to suppression and prevention of systemic disease. These studies reveal a mechanism of Treg cell-mediated suppression mediated by miRNA-containing exosomes. Overall design: Regulatory T cells (CD4+CD25hiFoxp3rfp+, Treg) were isolated from naive mice. RNA as extracted form some Treg cells, while others were cultured in complete IMDM media for 3 days, stimulated with anti-CD3 anti-CD3 (1ug/ml) and anti-CD28 (10ug/ml). Exosomes were recovered from Treg cell supernatant, as described, and RNA was extracted form the purified exosomes. To identify which miRNAs were transferred to Dicer-deficient (KO) cells from Treg cells, we cultured Dicer KO cells alone, or co-cultured Dicer KO cells with Treg cells. RNA was extracted form Dicer KO cells cultured alone or from Dicer KO cells cultured in the presence of Treg cells. 3 x biological replicates were used. Each biological replicate was derived from a pool of 3-5 samples.</long_description><repository>ENA</repository><description_synonyms>alpha-beta regulatory T-lymphocyte, suppressor T-cell, suppressor T cell., regulatory T lymphocyte, suppressor T-lymphocyte, Treg, suppressor T lymphocyte, alpha-beta regulatory T-cell, regulatory T-lymphocyte, alpha-beta regulatory T lymphocyte, CD4-positive, CD25-positive, regulatory T-cell</description_synonyms><name_synonyms>Mus musculus, Laboratory Mice., House, Mus, Laboratory, Swiss, Mus domesticus, mouse, Mus musculus domesticus, Swiss Mouse, mouse &lt;Mus musculus>, Mouse, House Mice, Swiss Mice, house mouse, Mice, Laboratory Mouse, House Mouse, mice C57BL/6xCBA/CaJ hybrid, domesticus, Mus muscaris</name_synonyms></additional><is_claimable>false</is_claimable><name>Mus musculus</name><description>miRNAs in Treg-derived Exosomes</description><dates><last_updated>2025-09-24</last_updated><first_public>2014-08-27</first_public></dates><accession>PRJNA259433</accession><cross_references><GEO>GSE60615</GEO><taxon>10090</taxon><PubMed>25035954</PubMed></cross_references></HashMap>