OBJECTIVE: The goal of this study was to analyze the role of aryl hydrocarbon receptor in peripheral blood CCR6(+)CD4(+) and CD4(+)CD25(+)T cells of patients with rheumatoid arthritis. METHODS: Flow cytometry was applied to determine the proportion of AhR positive cells in CCR6(+)CD4(+)T, CD4(+)CD25(+)T and peripheral blood peripheral mononuclear cells from each subject. AhR mRNA and CYP1A1 mRNA relative expression levels were tested by real-time PCR. RESULTS: The percentage of AhR positive cells in peripheral blood mononuclear cells was higher in RA group than that in healthy cases [(35.23±10.71)% vs. (18.83±7.32)%, p<0.01]. The expression levels of AhR and CYP1A1 were both increased in patients with RA while compared to controls [(3.71±1.63) vs. (2.00±1.27), p=0.002; (2.62±2.08) vs. (0.62±0.29), p<0.01, respectively]. In RA patients, the percentage of AhR positive cells in CD4(+)CD25(+)T cells was significantly lower than that from controls [17.90 (6.10±80.10)% vs. (52.49±19.18)%, p<0.01]; In healthy controls, the percentage of AhR positive cells in CD4(+)CD25(+)T cells was significantly higher than that in CCR6(+)CD4(+)T cells, and was also significantly higher than that in PBMCs [(52.49±19.18)% vs. (23.18±5.62)% vs. (18.06±7.80)%, X(2)=24.03, p<0.01]; in RA patients, the percentage of AhR positive cells in CCR6(+)CD4(+)T cells was significantly increased than that in CD4(+)CD25(+)T cells and PBMCs [(46.02±14.68)% vs. 17.90 (6.10±80.10)% vs. (34.22±10.33)%, X(2)=38.29, p<0.01]; Nevertheless, no statistically significant relationship was found between clinical data and AhR positive cells in CCR6(+)CD4(+)T and CD4(+)CD25(+)T cells. CONCLUSION: AhR may participate in the pathological progress of RA by controlling the differentiation of Th17 and Treg cells in peripheral blood.
CITATION STYLE
Cheng, L., Qian, L., Tan, Y., Wang, G.-S., Li, X.-M., Li, X.-P., & Luo, C.-Y. (2017). Unbalanced expression of aryl hydrocarbon receptor in peripheral blood CCR6 + CD4 + and CD4 + CD25 + T cells of rheumatoid arthritis. Revista Brasileira de Reumatologia (English Edition), 57(3), 190–196. https://doi.org/10.1016/j.rbre.2016.07.002
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