Altered microRNA Expression and Immunosuppressive Cytokine Production by Regulatory T Cells of Ulcerative Colitis Patients

被引:45
|
作者
Mohammadnia-Afrouzi, Mousa [1 ]
Hosseini, Ahmad Zavaran [1 ]
Khalili, Ali [2 ]
Abediankenari, Saeid [3 ]
Amari, Afshin [4 ]
Aghili, Babak [5 ]
Nataj, Hadi Hossein [2 ]
机构
[1] Tarbiat Modares Univ, Dept Immunol, Fac Med Sci, Tehran, Iran
[2] Mazandaran Univ Med Sci, Dept Immunol, Sari, Iran
[3] Mazandaran Univ Med Sci, Immunogenet Res Ctr, Sari, Iran
[4] Ahvaz Jundishapur Univ Med Sci, Dept Immunol, Fac Med, Ahvaz, Iran
[5] Univ Tehran Med Sci, Sch Med, Dept Immunol, Tehran, Iran
基金
美国国家科学基金会;
关键词
IL-10; IL-35; microRNA; regulatory T cells; ulcerative colitis; SUPPRESSIVE FUNCTION; SELF-TOLERANCE; FOXP3; DICER; AUTOIMMUNITY; INDUCTION; MIR-21; CD127; MICE; CD25;
D O I
10.3109/08820139.2015.1103749
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T (Treg) cells are essential for maintenance of peripheral tolerance and prevention of autoimmune diseases in part by producing immunosuppressive cytokines. Recently, microRNAs (miRNAs) have also been involved in autoimmune disorders, not least for their crucial role in the regulation of Treg biology and function. We simultaneously investigated the concentration of IL-35, IL-10, TGF-, and sCD25 in supernatant of cell culture and the expression patterns of several miRNAs in CD4(+)CD25(+) CD127(-/low) FoxP3(+) Tregs of ulcerative colitis (UC) patients. Significantly lower levels of IL-10 and IL-35 were observed in Treg cultures of UC patients. miR-21, miR-146a, and miR-155 levels were downregulated and miR-31 level was upregulated in Tregs of patients. Our results suggest that microRNAs may serve as a novel regulator in function and homoeostasis of UC Treg cells, providing a key role for them in pathophysiology of UC.
引用
收藏
页码:63 / 74
页数:12
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