Dr. Rolf M. Schwiete Center for Limbal Stem Cell and Aniridia Research, Homburg (Saar), Germany.
Department of Ophthalmology, Saarland University Medical Center, Homburg (Saar), Germany.
Invest Ophthalmol Vis Sci. 2022 Jul 8;63(8):7. doi: 10.1167/iovs.63.8.7.
Evaluation of mRNA and microRNA (miRNA) expression in epithelium and stroma of patients with keratoconus.
The epithelium and stroma of eight corneas of eight patients with keratoconus and eight corneas of eight non-keratoconus healthy controls were studied separately. RNA was extracted, and mRNA and miRNA analyses were performed using microarrays. Differentially expressed mRNAs and miRNAs in epithelial and stromal keratoconus samples compared to healthy controls were identified. Selected genes and miRNAs were further validated using RT-qPCR.
We discovered 170 epithelial and 1498 stromal deregulated protein-coding mRNAs in KC samples. In addition, in epithelial samples 180 miRNAs and in stromal samples 379 miRNAs were significantly deregulated more than twofold compared to controls. Pathway analysis revealed enrichment of metabolic and axon guidance pathways for epithelial cells and enrichment of metabolic, mitogen-activated protein kinase (MAPK), and focal adhesion pathways for stromal cells.
This study demonstrates significant differences in the expression and regulation of mRNAs and miRNAs in the epithelium and stroma of Patients with KC. Also, in addition to the well-known target candidates, we were able to identify further genes and miRNAs that may be associated with keratoconus. Signaling pathways influencing metabolic changes and cell contacts are affected in epithelial and stromal cells of patients with keratoconus.
评估圆锥角膜患者的上皮和基质中 mRNA 和 microRNA(miRNA)的表达。
分别研究了 8 例圆锥角膜患者和 8 例非圆锥角膜健康对照者的 8 个角膜的上皮和基质。提取 RNA,并使用微阵列进行 mRNA 和 miRNA 分析。与健康对照组相比,鉴定上皮和基质圆锥角膜样本中差异表达的 mRNA 和 miRNA。使用 RT-qPCR 进一步验证选定的基因和 miRNA。
我们在 KC 样本中发现了 170 个上皮和 1498 个基质下调的蛋白编码 mRNA。此外,在上皮样本中,有 180 个 miRNA,在基质样本中有 379 个 miRNA 与对照相比,差异表达超过两倍。通路分析显示,上皮细胞中代谢和轴突导向通路富集,而基质细胞中代谢、丝裂原活化蛋白激酶(MAPK)和焦点黏附通路富集。
本研究表明,在 KC 患者的上皮和基质中,mRNA 和 miRNA 的表达和调控存在显著差异。此外,除了众所周知的靶候选物外,我们还能够鉴定与圆锥角膜相关的其他基因和 miRNA。影响代谢变化和细胞接触的信号通路在上皮和基质细胞中受到影响。