4.7 Article

Up-regulation of microRNA-210 induces immune dysfunction via targeting FOXP3 in CD4+ T cells of psoriasis vulgaris

期刊

CLINICAL IMMUNOLOGY
卷 150, 期 1, 页码 22-30

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.clim.2013.10.009

关键词

Psoriasis vulgaris CD4(+) T cells; MicroRNA; FOXP3; Treg cells; miR-210

资金

  1. National Natural Science Foundation of China [81371743, 81270024]
  2. National Basic Research Program of China (973 Plan) [2009CB825605]
  3. Programs of Science-Technology Commission of Hunan province [2010FJ6032, 2011FJ3254, 07JJ3048]
  4. Fundamental Research Funds for the Central Universities

向作者/读者索取更多资源

Psoriasis vulgaris (PV) is a chronic inflammatory and T cell-mediated autoimmune skin disease. An immune dysfunction that is manifested by abnormally activated T cells and defective regulatory T (Treg) cells may play an important role in the pathogenesis of PV. However, the precise mechanism of the immune dysfunction in PV patients still remains unclear. In this study, we found that miR-210 expression is increased significantly in CD4(+) T cells from patients with PV and confirmed that FOXP3 is a target gene of miR-210. We also found that overexpression of miR-210 inhibits FOXP3 expression and impairs the immunosuppressive functions of Treg cells in CD4(+) T cells from healthy controls. In contrast, inhibition of miR-210 increases FOXP3 expression and reverses the immune dysfunction in CD4(+) T cells from patients with PV. Our data demonstrates that increased miR-210 induces immune dysfunction via by FOXP3 in CD4(+) T cells from patients with PV. (C) 2013 Elsevier Inc. All rights reserved.

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