Suppr超能文献

比较正常人眼角膜前基质层中高度近视和中度近视的蛋白表达。

Comparisons of the protein expressions between high myopia and moderate myopia on the anterior corneal stroma in human.

机构信息

Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, No. 1, Dongjiaomin Lane, Dongcheng District, Beijing, 100730, China.

出版信息

Graefes Arch Clin Exp Ophthalmol. 2023 Dec;261(12):3549-3558. doi: 10.1007/s00417-023-06158-2. Epub 2023 Jun 30.

Abstract

PURPOSE

To investigate the differentially expressed proteins (DEP) between high myopia and moderate myopia on the anterior corneal stroma.

METHODS

Tandem mass tag (TMT) quantitative proteomics was utilized to reveal proteins. DEPs were screened by the multiple change of more than 1.2 times or less than 0.83 and the P value < 0.05. The DEPs were functional annotated by Gene Ontology (GO) terms. Proteins and protein interaction (PPI) networks were conducted with String online tool. Parallel reaction monitoring (PRM) data processing was used to verify the TMT proteomics results.

RESULTS

There are 36 DEPs between high myopia and moderate myopia on the anterior corneal stroma, of which 11 proteins are upregulated, 25 proteins are downregulated. The GO analysis demonstrated keratinocyte migration and structural constituent of cytoskeleton that are significantly changed with most of the proteins decreased in high myopic corneas. Keratin 16 (KRT16) and erythrocyte membrane protein band 4.1-like protein 4B are the only two proteins involved in both functions. The PPI analysis showed keratin type II cytoskeletal 6A (KRT6A) and KRT16 that have strong connections. Immunoglobulin lambda variable 8-61(IGLV8-61) and nicotinamide phosphoribosyl transferase (NAMPT) have consistent results with the TMT.

CONCLUSIONS

The high myopic corneas have 36 DEPs compared to the moderate myopic corneas on the anterior corneal stroma. Keratinocyte migrations and structural constituent of cytoskeleton are weakened in high myopic corneas, which may partly account for the lower corneal biomechanics in high myopic eyes. The lower expressed KRT16 plays important roles in high myopic corneas.

摘要

目的

研究前角膜基质中高度近视和中度近视之间差异表达的蛋白质(DEP)。

方法

采用串联质量标签(TMT)定量蛋白质组学技术揭示蛋白质。通过变化倍数大于 1.2 倍或小于 0.83 倍且 P 值<0.05 筛选差异表达蛋白。通过基因本体论(GO)术语对差异表达蛋白进行功能注释。使用 String 在线工具进行蛋白质和蛋白质相互作用(PPI)网络分析。使用平行反应监测(PRM)数据处理来验证 TMT 蛋白质组学结果。

结果

在前角膜基质中,高度近视和中度近视之间有 36 个 DEP,其中 11 个蛋白上调,25 个蛋白下调。GO 分析表明,角蛋白细胞迁移和细胞骨架的结构成分发生了显著变化,大多数蛋白质在高度近视眼角膜中减少。角蛋白 16(KRT16)和红细胞膜蛋白带 4.1 样蛋白 4B 是仅有的两个参与这两个功能的蛋白。PPI 分析表明角蛋白 II 细胞骨架 6A(KRT6A)和 KRT16 具有较强的联系。免疫球蛋白轻链可变 8-61(IGLV8-61)和烟酰胺磷酸核糖转移酶(NAMPT)与 TMT 具有一致的结果。

结论

与中度近视眼角膜相比,高度近视眼角膜前角膜基质中有 36 个 DEP。角蛋白细胞迁移和细胞骨架的结构成分在高度近视眼角膜中减弱,这可能部分解释了高度近视眼中较低的角膜生物力学。低表达的 KRT16 在高度近视眼角膜中发挥重要作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验