MicroRNA-146a-5p enhances T helper 17 cell differentiation via decreasing a disintegrin and metalloprotease 17 level in primary sjögren's syndrome

• Published in: Bioengineered Vol. 12; no. 1; pp. 310 - 324
• Main Authors: Wang, Xiaoyan, Xin, Shaojun, Wang, Youqing, Ju, Duo, Wu, Quan, Qiu, Ye, Niu, Xuemin, Liu, Wei, Li, Jianyou, Ji, Pengtian
• Format: Journal Article
• Language: English
• Published: United States Taylor & Francis 01.01.2021
• Subjects: adam17; ADAM17 Protein - genetics; ADAM17 Protein - metabolism; Adult; Cell Differentiation - genetics; Humans; il-23/IL-23R signaling; Interleukin-23 - genetics; Interleukin-23 - metabolism; Leukocytes, Mononuclear - metabolism; MicroRNAs - blood; MicroRNAs - genetics; MicroRNAs - metabolism; Middle Aged; mir-146a-5p; Primary sjögren's syndrome; Receptors, Interleukin - genetics; Receptors, Interleukin - metabolism; Research Paper; Sjogren's Syndrome - genetics; Sjogren's Syndrome - metabolism; th17 cell differentiation; Th17 Cells - cytology; Th17 Cells - metabolism; Young Adult; adam17; Primary sjögren’s syndrome; il-23/IL-23R signaling; mir-146a-5p; th17 cell differentiation
• DOI: 10.1080/21655979.2020.1870321
• ISSN: 2165-5979; 2165-5987

In clinical practice, we found that microRNA (miR)-146a-5p is significantly up-regulated in peripheral blood mononuclear cells (PBMCs) of primary sjögren's syndrome (pSS) patients. In vitro experiments confirmed that miR-146a-5p promotes T helper 17 (Th17) cell differentiation, but the specific mechanism is still unknown. To solve this problem, 20 pSS patients and 20 healthy subjects were enrolled in this study and PBMCs were isolated from their blood. The expression of the membrane IL-23 R (mIL-23 R) in PBMCs was determined. CD3 + T cells were also isolated and used to further analyze the relationship between the ectodomain shedding of mIL-23 R and a disintegrin and metalloprotease 17 (ADAM17). Finally, miR-146a-5p inhibitor and mimics were transfected into PBMCs to evaluate the relationship between ADAM17 and mIL-23 R, and explore the role of mIL-23 R and ADAM17 in Th17 cell differentiation. Our results revealed a significantly increased expression of miR-146a-5p in PBMCs from pSS patients and significantly increased percentage of Th17 cells compared to PBMCs from healthy controls. Under polarization culture conditions, pSS patient-derived PBMCs can more easily differentiate into Th17 cells, which was, to a great extent, attributable to the increased expression of mIL-23 R. Moreover, ADAM17, an ectodomain sheddase of mIL-23 R, was targeted and negatively regulated by miR-146a-5p, which reduced the ectodomain shedding of mIL-23 R. Overall, our results suggested that miR-146a-5p could promote Th17 cell differentiation through targeting and negatively regulating ADAM17. Thus, these results might offer a new approach in the treatment of pSS.