Ueta Mayumi, Nishigaki Hiromi, Komai Seitaro, Mizushima Katsura, Tamagawa-Mineoka Risa, Naito Yuji, Katoh Norito, Sotozono Chie, Kinoshita Shigeru
Department of Ophthalmology, Kyoto, Japan.
Department of Human Immunology and Nutrition Science, Kyoto, Japan.
Front Genet. 2023 Jan 6;13:1025539. doi: 10.3389/fgene.2022.1025539. eCollection 2022.
We have hypothesized that different factors are involved in the severity of ACD and AD because some but not all patients with atopic dermatitis (AD) present with allergic conjunctival disease (ACD) including severe types such as atopic keratoconjunctivitis (AKC) with/without giant papillae. We previously reported that plasma miR-628-3p was up-regulated in AD with severe ACD, but not in severe AD without severe ACD or in our healthy controls. In this study, to investigate the pathogenesis of AD with and without severe ACD, we performed comprehensive plasma miRNA analysis and studied the function of some miRNAs which were significantly up-regulated in ACD. Transcriptomics analysis of miRNA was performed using the microarray platform from the plasma of nine individuals (AD, severe ACD, controls: = 3 each). To confirm up-regulation of the 12 miRNAs of the eight miRNA groups we focused on, we performed quantitative miRNA polymerase chain reaction (PCR) assays using 80 plasma samples (AD: 23, severe ACD: 17, controls: 40). To study the function of the eight miRNAs which were significantly up-regulated in ACD, we transfected their mimic to THP-1 cells, a monocyte cell line, and performed comprehensive gene expression analysis of them. The up-regulation of gene expression of interest in transfected THP-1 cells with the hsa-let-7a-5p miRNA mimic was confirmed by quantitative RT-qPCR assay. Quantitative miRNA PCR assays showed that hsa-let-7a-5p, hsa-let-7days-3p, hsa-let-7e-5p, and hsa-miR-151a-5p were significantly up-regulated in both AD-ACD and AD-ACD as were hsa-miR-130a-3p, hsa-miR-151a-3p, has-miR-27b-3p, and hsa-miR-146a-5p in AD-ACD but not in AD-ACD . The functions of each miRNA were investigated by comprehensive gene expression analysis of THP-1 cells transfected with each miRNA mimic. Of the eight miRNAs, hsa-let-7a-5p, hsa-let-7e-5p, has-miR-27b-3p, and hsa-miR-146a-5p mimic-transfected THP-1 cells showed the up-regulation of CXCL10 (IP-10; interferon gamma-induced protein 10), which might be one of the innate immune-related genes. Quantitative RT-qPCR assays of transfected THP-1 cells with the hsa-let-7a-5p miRNA mimic showed that the 17 genes up-regulated more than 10-fold in the comprehensive gene expression analysis, and TLR3, RIG-I, and MDA5, important innate immune-related genes, were significantly up-regulated. TNFSF13B, AIM2, USP41, STAP1, GBP4, CCL8, and IFI27, reportedly down-regulated by the hsa-miR-628-3p mimic, were also significantly up-regulated in the transfected cells. Hsa-let-7a-5p, which was significantly up-regulated in AD-ACD and AD-ACD , could positively regulate the important innate immune-related genes such as TLR3, RIG-I, and MDA5. It is possible that in an allergic disease such as atopic keratoconjunctivitis and/or dermatitis, innate immune responses might be positively regulated by hsa-let-7a-5p in the plasma.
我们推测,不同因素与变应性接触性皮炎(ACD)和特应性皮炎(AD)的严重程度有关,因为部分但并非所有特应性皮炎(AD)患者会出现变应性结膜疾病(ACD),包括严重类型,如伴有/不伴有巨大乳头的特应性角结膜炎(AKC)。我们之前报道过,血浆miR - 628 - 3p在伴有严重ACD的AD患者中上调,但在不伴有严重ACD的重度AD患者或健康对照中未上调。在本研究中,为了探究伴有和不伴有严重ACD的AD的发病机制,我们进行了全面的血浆miRNA分析,并研究了在ACD中显著上调的一些miRNA的功能。使用来自9名个体(AD、严重ACD、对照:各3名)血浆的微阵列平台进行miRNA的转录组学分析。为了确认我们关注的8个miRNA组中12个miRNA的上调情况,我们使用80份血浆样本(AD:23份,严重ACD:17份,对照:40份)进行了定量miRNA聚合酶链反应(PCR)检测。为了研究在ACD中显著上调的8个miRNA的功能,我们将它们的模拟物转染至单核细胞系THP - 1细胞,并对其进行全面的基因表达分析。通过定量RT - qPCR检测证实了用hsa - let - 7a - 5p miRNA模拟物转染的THP - 1细胞中感兴趣基因的表达上调。定量miRNA PCR检测显示hsa - let - 7a - 5p、hsa - let - 7d - 3p、hsa - let - 7e - 5p和hsa - miR - 151a - 5p在AD - ACD⁺和AD - ACD⁻中均显著上调,hsa - miR - 130a - 3p、hsa - miR - 151a - 3p、has - miR - 27b - 3p和hsa - miR - 146a - 初级5p在AD - ACD⁺中显著上调,但在AD - ACD⁻中未上调。通过对用每个miRNA模拟物转染的THP - 1细胞进行全面的基因表达分析来研究每个miRNA的功能。在这8个miRNA中,用hsa - let - 7a - 5p、hsa - let - 7e - 5p、has - miR - 27b - 3p和hsa - miR - 146a - 5p模拟物转染的THP - 1细胞显示CXCL10(IP - 10;干扰素γ诱导蛋白10)上调,其可能是先天免疫相关基因之一。用hsa - let - 7a - 5p miRNA模拟物转染的THP - 1细胞的定量RT - qPCR检测显示,在全面的基因表达分析中上调超过10倍的17个基因以及重要的先天免疫相关基因TLR3、RIG - I和MDA5均显著上调。据报道被hsa - miR - 628 - 3p模拟物下调的TNFSF13B、AIM2、USP41、STAP1、GBP4、CCL8和IFI27在转染细胞中也显著上调。在AD - ACD⁺和AD - ACD⁻中均显著上调 的hsa - let - 7a - 5p可正向调节重要的先天免疫相关基因,如TLR3、RIG - I和MDA5。在诸如特应性角结膜炎和/或皮炎等变应性疾病中,血浆中的hsa - let - 7a - 5p可能正向调节先天免疫反应。