Department of Immunology, Instituto de Investigación Sanitaria Fundación Jiménez Díaz (IIS-FJD, UAM), 28040 Madrid, Spain.
Centro de Investigación Biomédica en Red (CIBER) de Enfermedades Respiratorias (CIBERES), 28029 Madrid, Spain.
Cells. 2022 Sep 2;11(17):2746. doi: 10.3390/cells11172746.
Respiratory diseases such as bronchiolitis, and those with wheezing episodes, are highly important during infancy due to their potential chronicity. Immune response dysregulation is critical in perpetuating lung damage. Epigenetic modifications including microRNA (miRNA) post-transcriptional regulation are among the factors involved in alleviating inflammation. We evaluated the expression of miR-146a-5p, a previously described negative regulator of immunity, in infants with respiratory diseases, in order to study epigenetic regulation of the immune response. Nasopharyngeal aspirate (NPA) was obtained from infants with bronchiolitis (ongoing and post-disease) or with wheezing episodes in addition to healthy controls. Virus presence was determined by nested PCR, while miRNA and gene expression were studied in cells from NPAs using qPCR. Healthy small airway epithelial cells (SAECs) were used as an in vitro model. We observe a reduction in miR-146a-5p expression in infants with either of the two diseases compared to controls, suggesting the potential of this miRNA as a disease biomarker. Post-bronchiolitis, miR-146a-5p expression increases, though without reaching levels of healthy controls. MiR-146a-5p expression correlates inversely with the immune-related gene , while its expression correlates directly with . When heathy donor SAECs are stimulated by poly:IC, we observe an increase in miR-146a-5p, with wounds having a synergistic effect. In conclusion, infants with respiratory diseases present reduced miR-146a-5p expression, possibly affecting immune dysregulation.
呼吸道疾病,如细支气管炎和喘息发作,在婴儿期因其潜在的慢性而非常重要。免疫反应失调在持续肺损伤中起着关键作用。表观遗传修饰,包括 microRNA (miRNA) 转录后调控,是缓解炎症的相关因素之一。我们评估了 miR-146a-5p 的表达,miR-146a-5p 是一种先前描述的免疫负调节剂,在患有呼吸道疾病的婴儿中,以研究免疫反应的表观遗传调节。我们从患有细支气管炎(持续期和疾病后)或喘息发作的婴儿以及健康对照中获得了鼻咽抽吸物(NPA)。通过巢式 PCR 确定病毒存在,同时使用 qPCR 研究 NPA 中的 miRNA 和基因表达。健康的小气道上皮细胞(SAEC)被用作体外模型。我们观察到与对照组相比,两种疾病中的婴儿 miR-146a-5p 的表达降低,表明该 miRNA 作为疾病生物标志物的潜力。细支气管炎后,miR-146a-5p 的表达增加,但仍未达到健康对照组的水平。miR-146a-5p 的表达与免疫相关基因呈负相关,而与呈正相关。当健康供体 SAEC 受到 poly:IC 刺激时,我们观察到 miR-146a-5p 增加,而伤口具有协同作用。总之,患有呼吸道疾病的婴儿存在 miR-146a-5p 表达降低的情况,可能影响免疫失调。