Upregulation of miR‐9 and miR‐193b over human Th17 cell differentiation

BACKGROUND: Th17 cells are a newly discovered subset of CD4(+) T cells known as key participants in various immune responses and inflammatory conditions including autoimmune diseases. Mi(cro)RNAs are a family of non‐coding RNAs that regulate numerous critical immune functions. Immuno‐miRNAs modulate cell biological processes in T cells, such as differentiation and function of Th17 cells. The aim of the present study is to investigate the expression of miR‐9‐5p, miR‐193b‐3p, and autoimmunity‐related genes during human Th17 cells differentiation. METHODS: Human naïve CD4(+) T cells were purified from peripheral blood mononuclear cells (PBMCs) by magnetic cell sorting system (MACS) and their purity was checked by flow‐cytometric analysis. Naïve CD4(+) T cells were cultured under Th17‐polarizing condition for 6 days. IL‐ 17 secretion was determined by means of enzyme‐linked immunosorbent assay (ELISA). Next, the expression levels of miRNAs and putative targets genes were assessed by qRT‐PCR at different time points of differentiation. RESULTS: Our result showed dramatic downregulation of TCF7, MAP3K1, ENTPD1, and NT5E genes during human Th17 differentiation. Polarization also had a significant inducible effect on the expression of miR‐9 and miR‐193b over differentiation of human Th17 cells. According to our results, miR‐9‐5p and miR‐193b‐3p may contribute to Th17 differentiation probably by inhibiting the expression of negative regulators of Th17 differentiation. CONCLUSION: This study confirmed deregulation of TCF7, MAP3K1, ENTPD1, and NT5E genes in Th17 differentiation process and introduced miR‐9 and miR‐193b as Th17 cell‐associated miRNAs, making them good candidates for further investigations.