The Regenerative Medicine Unit, Department of Medical Biochemistry, Oslo University Hospital, Ullevål, 0450 Oslo, Norway.
Blood Cell Research Group, Department of Medical Biochemistry, Oslo University Hospital, Ullevål, 0450 Oslo, Norway.
Int J Mol Sci. 2023 Oct 20;24(20):15390. doi: 10.3390/ijms242015390.
Currently, diagnosing and stratifying dry eye disease (DED) require multiple tests, motivating interest in a single definitive test. The purpose of this study was to investigate the potential for using tear fluid extracellular vesicle (EV)-RNA in DED diagnostics. With a role in intercellular communication, nanosized EVs facilitate the protected transport of diverse bioactive molecules in biofluids, including tears. Schirmer strips were used to collect tears from 10 patients presenting with dry eye-related symptoms at the Norwegian Dry Eye Clinic. The samples comprised two groups, five from patients with a tear film break-up time (TBUT) of 2 s and five from patients with a TBUT of 10 s. Tear fluid EV-RNA was isolated using a Qiagen exoRNeasy Midi Kit, and the RNA was characterized using Affymetrix Clariom D microarrays. The mean signal values of the two groups were compared using a one-way ANOVA. A total of 26,639 different RNA transcripts were identified, comprising both mRNA and ncRNA subtypes. Approximately 6% of transcripts showed statistically significant differential abundance between the two groups. The mRNA sodium channel modifier 1 (SCNM1) was detected at a level 3.8 times lower, and the immature microRNA-130b was detected at a level 1.5 times higher in the group with TBUT 2 s compared to the group with TBUT 10 s. This study demonstrates the potential for using tear fluid EV-RNA in DED diagnostics.
目前,干眼病(DED)的诊断和分层需要多种测试,这促使人们对单一的明确测试产生了兴趣。本研究的目的是探讨使用泪液细胞外囊泡(EV)-RNA 进行 DED 诊断的潜力。EV 作为细胞间通讯的一种方式,纳米级 EV 促进了生物体液中包括眼泪在内的各种生物活性分子的保护运输。Schirmer 条用于从挪威干眼诊所出现干眼相关症状的 10 名患者中收集眼泪。这些样本包括两组,一组来自 TBUT 为 2 秒的患者,一组来自 TBUT 为 10 秒的患者。使用 Qiagen exoRNeasy Midi Kit 分离泪液 EV-RNA,并使用 Affymetrix Clariom D microarrays 对 RNA 进行表征。使用单向 ANOVA 比较两组的平均信号值。共鉴定出 26639 种不同的 RNA 转录本,包括 mRNA 和 ncRNA 亚型。两组之间约有 6%的转录本显示出统计学上的显著差异丰度。与 TBUT 为 10 秒的组相比,TBUT 为 2 秒的组中钠离子通道调节剂 1(SCNM1)的检测水平低 3.8 倍,不成熟 microRNA-130b 的检测水平高 1.5 倍。本研究表明,使用泪液 EV-RNA 进行 DED 诊断具有潜力。