MicroRNA‐126 deficiency enhanced the activation and function of CD4+T cells by elevating IRS‐1 pathway. (30th October 2017)

• Record Type: Journal Article
• Authors: Chu, F.; Hu, Y.; Zhou, Y.; Guo, M.; Lu, J.; Zheng, W.; Xu, H.; Zhao, J.; Xu, L.
• Is Part Of: Clinical and experimental immunology. Volume 191:Number 2(2018:Feb.)
• Page Start: 166
• Page End: 179
• Publication Date: 2017-10-30
• Subjects: CD4+ T cell -- cytokines -- DSS -- IRS‐1 -- miR‐126; Immunopathology -- Periodicals; 616.079
• DOI: 10.1111/cei.13067
• Languages: English
• ISSNs: 0009-9104

Abstract

Summary: Recent evidence has shown that microRNA‐126 (miR‐126) has been involved in the development and function of immune cells, which contributed to the pathogenesis of related clinical diseases. However, the potential role of miR‐126 in the development and function of CD4 + T cells remains largely unknown. Here we first found that the activation and proliferation, as well as the expression of interferon (IFN)‐γ, of CD4 + T cells from miR‐126 knock‐down (KD) mice using the miRNA‐sponge technique were enhanced significantly in vitro, compared with those in CD4 + T cells from wild‐type (WT) mice. To monitor further the possible effect of miR‐126 deficiency on the function of CD4 + T cells in vivo, we used dextran sulphate sodium (DSS)‐induced murine model of acute autoimmune colitis and found that miR‐126 deficiency could elevate the pathology of colitis. Importantly, the proportion of CD4 + T cells in splenocytes increased significantly in miR‐126KD mice. Moreover, the expression levels of CD69 and CD44 on CD4 + T cells increased significantly and the expression level of CD62L decreased significantly. Of note, adoptive cell transfer assay showed that the pathology of colitis was more serious in carboxyfluorescein succinimidyl ester (CFSE)‐labelled miR‐126KD CD4 + T cell‐transferred group, compared with that in the CFSE‐labelled WT CD4 + T cells transferred group. Consistently, the expression levels of CD69 and CD44 on CFSE + cells increased significantly. Furthermore, both the proliferation and IFN‐γ secretion of CFSE + cells also increased significantly in the CFSE‐labelled miR‐126KD CD4 + T cell‐transferred group. Mechanistic evidence showed that the expression of insulin receptor substrate 1 (IRS‐1), as a functional target of miR‐126, was elevated in CD4 + T cells from miR‐126KD mice, accompanied by altered transduction of the extracellular regulated kinase, protein B (AKT) and nuclear factor kappa B (NF‐κB) pathway. Our data revealed a novel role in which miR‐126 was an intrinsic regulator in the function of CD4 + T cells, which provided preliminary basis for exploring further the role of miR‐126 in the development, function of CD4 + T cells and related clinical diseases. Abstract : MiR‐126 deficiency enhanced the activation and function of CD4 + T cells through elevating IRS‐1 pathway. MiR‐126 deficiency promoted the pathology of colitis in dextran sulfate sodium (DSS)‐induced murine model of acute autoimmune colitis, which was related to the altered activation and function of CD4 + T cells. These data revealed that miR‐126 was a novel intrinsic regulator in the activation and function of CD4 + T cells, which provided preliminary basis for further exploring on the role of miR‐126 in the development and function of CD4 + T cells, as well as related clinical diseases.