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Circulating microRNA Expression Profiling Identifies miR-125a-5p Promoting T Helper 1 Cells Response in the
Yingzhao Liu1, Xiangmei Ding1, Si Xiong2
1Department of Endocrinology, The Affiliated People's Hospital of Jiangsu University, Zhenjiang Medical School of Nanjing Medical University, Zhenjiang, China.
Abstract:
MicroRNAs (miRNAs) have emerged as key regulators of cellular processes by suppressing target mRNAs at the posttranscriptional level. However, little is known regarding the expression of miRNAs in peripheral blood mononuclear cells (PBMCs) from Hashimoto's thyroiditis (HT) patients. Therefore, 38 HT patients and 36 healthy volunteers were enrolled in this study to identify HT-mediated changes in miRNA expression. Over 1,000 dysregulated miRNAs and their biological functions in the HT patients were identified. Among them, miR-125a-5p expression was upregulated and inversely correlated with low levels of MAF, a transcription factor that inhibits Th1 cells activity and the production of IFN-γ. Luciferase assay results demonstrated that MAF is a direct target gene of miR-125a-5p. Moreover, the proportion of circulating Th1 cells and the transcript levels of IFN-γ were increased in the HT patients. MiR-125a-5p expression positively correlated with the proportion of circulating Th1 cells and the serum concentrations of anti-thyroperoxidase antibodies in the HT patients. Interestingly, knockdown of miR-125a-5p in CD4+ T cells resulted in an elevated level of MAF but decreased the proportion of Th1 cells and the transcript level of IFN-γ in vitro. Furthermore, upregulated miR-125a-5p and IFN-γ transcript levels and downregulated MAF expression were detected in thyroid tissues from HT patients. Receiver operating characteristic (ROC) curves suggested that miR-125a-5p has a crucial role in the HT. Our results demonstrate that the elevated levels of miR-125a-5p contribute to the Th1 cells response in the HT patients and may be involved in the pathogenesis of HT.
Insights
Elevated miR-125a-5p in Hashimoto's thyroiditis (HT) patients promotes Th1 cell responses. This microRNA targets MAF, potentially driving HT pathogenesis by increasing IFN-γ production.
Area of Science:
- Immunology
- Molecular Biology
- Endocrinology
Background:
- MicroRNAs (miRNAs) regulate gene expression posttranscriptionally.
- The role of miRNAs in Hashimoto's thyroiditis (HT) pathogenesis is largely unknown.
- Peripheral blood mononuclear cells (PBMCs) are crucial in autoimmune responses.
Purpose of the Study:
- To identify miRNA expression changes in PBMCs from HT patients.
- To investigate the functional role of dysregulated miRNAs in HT.
- To explore the relationship between specific miRNAs and immune cell activity in HT.
Main Methods:
- Expression profiling of over 1,000 miRNAs in HT patients and healthy controls.
- Luciferase assays to confirm miRNA-target interactions.
- Analysis of Th1 cell proportions, IFN-γ transcript levels, and MAF expression in patient samples and cell cultures.
- ROC curve analysis for diagnostic potential.
Main Results:
- miR-125a-5p was significantly upregulated in HT patients.
- MAF was identified as a direct target of miR-125a-5p, with its expression inversely correlated with miR-125a-5p.
- Increased Th1 cell proportion and IFN-γ levels were observed in HT patients, correlating with miR-125a-5p levels.
- In vitro experiments confirmed miR-125a-5p knockdown reduced Th1 cells and IFN-γ production.
- Upregulated miR-125a-5p and IFN-γ, and downregulated MAF were found in thyroid tissues.
Conclusions:
- Elevated miR-125a-5p contributes to the Th1 cell-mediated immune response in Hashimoto's thyroiditis.
- miR-125a-5p may play a significant role in the pathogenesis of HT.
- miR-125a-5p shows potential as a biomarker for HT.
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