microRNA-342, microRNA-191 and microRNA-510 are differentially expressed in T regulatory cells of type 1 diabetic patients
Language English Country Netherlands Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19954774
DOI
10.1016/j.cellimm.2009.10.012
PII: S0008-8749(09)00193-2
Knihovny.cz E-resources
- MeSH
- Diabetes Mellitus, Type 1 blood genetics MeSH
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- MicroRNAs genetics MeSH
- Young Adult MeSH
- T-Lymphocytes, Regulatory metabolism MeSH
- Oligonucleotide Array Sequence Analysis methods MeSH
- Cluster Analysis MeSH
- Gene Expression Profiling * MeSH
- T-Lymphocytes metabolism MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- MicroRNAs MeSH
- MIRN191 microRNA, human MeSH Browser
- MIRN342 microRNA, human MeSH Browser
- MIRN510 microRNA, human MeSH Browser
Regulatory T cells (Tregs) are critical regulators of autoimmune diseases, including type 1 diabetes mellitus. It is hypothesised that Tregs' function can be influenced by changes in the expression of specific microRNAs (miRNAs). Thus, we performed miRNAs profiling in a population of Tregs separated from peripheral blood of five type 1 diabetic patients and six healthy donors. For more detailed molecular characterisation of Tregs, we additionally compared miRNAs expression profiles of Tregs and conventional T cells. Tregs were isolated according to CD3+, CD4+, CD25(hi)+ and CD127- by flow cytometry, and miRNA expression profiling was performed using TaqMan Array Human MicroRNA Panel-1 (384-well low density array). In Tregs of diabetic patients we found significantly increased expression of miRNA-510 (p=0.05) and decreased expression of both miRNA-342 (p<0.0001) and miRNA-191 (p=0.0079). When comparing Tregs and T cells, we revealed that Tregs had significant higher expression of miRNA-146a and lower expression of eight specific miRNAs (20b, 31, 99a, 100, 125b, 151, 335, and 365). To our knowledge, this is the first study demonstrating changes in miRNA expression profiles occurring in Tregs of T1D patients and a miRNAs signature of adult Tregs.
References provided by Crossref.org
Epigenetic Regulation in Etiology of Type 1 Diabetes Mellitus