4.6 Article

miR-146a enhances regulatory T-cell differentiation and function in allergic rhinitis by targeting STAT5b

Journal

ALLERGY
Volume 77, Issue 2, Pages 550-558

Publisher

WILEY
DOI: 10.1111/all.15163

Keywords

allergic rhinitis; miR-146a; STAT5b; Treg cells

Funding

  1. National Natural Science Foundation of China [82071021, 81670907]
  2. Key R&D Project of Shandong Province [2020CXGC011302]

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The study found that expression levels of miR-146a and STAT5b were significantly lower in the nasal mucosa or PBMCs of AR patients compared to the control group. There were fewer Tregs in miR-146a knockdown or STAT5b knockdown PBMCs, and miR-146a positively targeted STAT5b to enhance Treg differentiation and function in AR.
Background MicroRNA (miR)-146a, as an important immune regulatory factor with an anti-inflammatory effect, plays a crucial role in regulatory T-cell (Tregs) differentiation and function in allergic rhinitis (AR). The present study aimed to investigate the regulatory mechanism employed by miR-146a to control Treg differentiation and function in AR. Methods Expression of miR-146a and STAT5b in peripheral blood mononuclear cells (PBMCs) and nasal mucosa from patients with AR was detected by qPCR and Western blotting. Tregs were quantified by flow cytometry in miR-146a knockdown or STAT5b knockdown PBMCs. FOXP3, IL-10, and TGF-beta levels were detected by Western blotting or ELISA in miR-146a knockdown or STAT5b overexpressing PBMCs, as well as in STAT5b knockdown PBMCs overexpressing miR-146a. The effect of miR-146a on STAT5b was observed by luciferase assay and knockdown experiments. Results Levels of miR146a and STAT5b in the nasal mucosa or PBMCs were significantly lower in the AR group than in the control group. There were significantly fewer Tregs in miR-146a knockdown or STAT5b knockdown PBMCs compared to control PBMCs. Expression of FOXP3, IL-10, and TGF-beta was decreased in the miR-146a knockdown group but increased in the STAT5b overexpression group. In contrast, miR-146a overexpression increased the levels of these factors, but knockdown of STAT5b significantly inhibited this effect. Luciferase assay and knockdown experiments showed that miR-146a bound directly to STAT5b. Conclusions miR-146a enhances Treg differentiation and function in AR by positively targeting STAT5b.

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