Abstract

Uveitis is a serious eye disease that usually damages young adult's health. MicroRNAs (miRNAs) are a class of small noncoding RNAs which regulate messenger RNA (mRNA) expression. It is predicted that rno-miR-30b-5p can regulate the expressions of interleukin-10 (IL-10) and Toll-like receptor 4 (TLR4). In this study, the regulatory role of rno-miR-30b-5p in IL-10 and TLR4 gene expressions was validated using luciferase activity assay. Further, the inflammatory manifestation of the anterior segment and pathological examination of the eye were explored in experimental autoimmune uveitis (EAU) rats. Meanwhile, the levels of rno-miR-30b-5p in eye tissues, spleen, and lymph nodes were measured using quantitative PCR (Q-PCR). IL-10 and TLR4 in spleen and lymph nodes were further separately determined by using Q-PCR and Enzyme-Linked Immunosorbent Assay (ELISA). Moreover, rno-miR-30b-5p mimic and its inhibitor were separately transfected into purified T cells, and the levels of IL-10 and TLR4 were detected using PCR, flow cytometry, and ELISA techniques. Results indicate that rno-miR-30b-5p was downregulated in spleen, lymph nodes, and eye tissues whereas the expressions of IL-10 and TLR4 at mRNA and protein levels were upregulated. The levels of IL-10 and TLR4 were negatively correlated to rno-miR-30b-5p levels. The result of in vitro cell transfection experiment indicates that IL-10 and TLR4 expressions were inhibited at mRNA and protein levels after T cells incubated with rno-miR-30b-5p mimic. However, the IL-10 and TLR4 mRNA levels were upregulated in purified T cells from spleen and lymph nodes after treatment with miR-30b-5p antagonist. In addition, there was no evident change of IL-10 and TLR4 proteins in spleen and lymph node T cells between EAU control and negative treatment groups. Flow cytometry analysis revealed that rno-miR-30b-5p mimic could reduce the number of both IL-10 and TLR4 positive cells, whereas rno-miR-30b-5p inhibitor could increase the number of IL-10 and TLR4 positive cells. Our study demonstrates that rno-miR-30b-5p influences the development of uveitis by regulating the level of IL-10 and TLR4 positive cells, thereby playing a role in the pathogenesis of uveitis.

Highlights

  • Uveitis is a complicated inflammatory disease of the uvea that is considered to be one of the important causes of blindness in the world [1, 2], which is usually classified according to the anatomical location of inflammation into anterior, intermediate, posterior, and panuveitis

  • All these findings suggest that both Toll-like receptor 4 (TLR4) and interleukin 10 (IL-10) play a critical role in the pathogenesis of uveitis

  • The results show that the levels of rno-miR-30b-5p in eye, spleen, and lymph nodes tissues in experimental autoimmune uveitis (EAU) rats had a marked downregulation (P < 0 01, Figure 2) as compared with those of NC and Complete Freund’s Adjuvant (CFA) + TB groups, respectively, indicating that rno-miR30b-5p plays an important role in the pathogenesis of EAU

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Summary

Introduction

Uveitis is a complicated inflammatory disease of the uvea that is considered to be one of the important causes of blindness in the world [1, 2], which is usually classified according to the anatomical location of inflammation into anterior, intermediate, posterior, and panuveitis. Interleukin 10 (IL-10) plays a protective role in a mouse experimental autoimmune uveoretinitis model and is upregulated in human uveitis patients [13,14,15]. Recent research shows that IL-10 levels were elevated in serum in EAU rats [17], while the IL-10 mRNA levels were increased in spleen and lymph nodes tissue [18]. All these findings suggest that both TLR4 and IL-10 play a critical role in the pathogenesis of uveitis

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