Mok Jeong-Hun, Park Do Young, Han Jong Chul
Department of Medical Device Management and Research, SAIHST, Sungkyunkwan University, Seoul, Korea.
Department of Ophthalmology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Biofactors. 2024 Nov-Dec;50(6):1220-1235. doi: 10.1002/biof.2079. Epub 2024 May 31.
Various substances within the aqueous humor (AH) can directly or indirectly impact intraocular tissues associated with intraocular pressure (IOP), a critical factor in glaucoma development. This study aims to investigate individual changes in these AH substances and the interactions among altered components through a multi-omics approach. LC/MS analysis was conducted on AH samples from patients with exfoliation syndrome (XFS, n = 5), exfoliation glaucoma (XFG, n = 4), primary open-angle glaucoma (POAG, n = 11), and cataracts (control group, n = 7). Subsequently, differentially expressed proteins and metabolites among groups, alterations in their network interactions, and their biological functions were examined. Both data-independent acquisition and data-dependent acquisition methods were employed to analyze the AH proteome and metabolome, and the results were integrated for a comprehensive analysis. In the proteomics analysis, proteins upregulated in both the XFG and POAG groups were associated with lipid metabolism, complement activation, and extracellular matrix regulation. Metabolomic analysis highlighted significant changes in amino acids related to antioxidant processes in the glaucoma groups. Notably, VTN, APOA1, C6, and L-phenylalanine exhibited significant alterations in the glaucoma groups. Integration of individual omics analyses demonstrated that substances associated with inflammation and lipid metabolism, altered in the glaucoma groups, showed robust interactions within a complex network involving PLG, APOA1, and L-phenylalanine or C3, APOD, and L-valine. These findings offer valuable insights into the molecular mechanisms governing IOP regulation and may contribute to the development of new biomarkers for managing glaucoma.
房水(AH)中的各种物质可直接或间接影响与眼压(IOP)相关的眼内组织,眼压是青光眼发展的关键因素。本研究旨在通过多组学方法研究这些房水物质的个体变化以及改变的成分之间的相互作用。对剥脱综合征(XFS,n = 5)、剥脱性青光眼(XFG,n = 4)、原发性开角型青光眼(POAG,n = 11)和白内障患者(对照组,n = 7)的房水样本进行了液相色谱/质谱(LC/MS)分析。随后,研究了各组之间差异表达的蛋白质和代谢物、它们网络相互作用的改变以及它们的生物学功能。采用数据非依赖采集和数据依赖采集方法分析房水蛋白质组和代谢组,并将结果整合进行综合分析。在蛋白质组学分析中,XFG组和POAG组中上调的蛋白质与脂质代谢、补体激活和细胞外基质调节有关。代谢组学分析突出了青光眼组中与抗氧化过程相关的氨基酸的显著变化。值得注意的是,VTN、APOA1、C6和L-苯丙氨酸在青光眼组中表现出显著改变。个体组学分析的整合表明,青光眼组中与炎症和脂质代谢相关的物质在涉及PLG、APOA1和L-苯丙氨酸或C3、APOD和L-缬氨酸的复杂网络中表现出强烈的相互作用。这些发现为眼压调节的分子机制提供了有价值的见解,并可能有助于开发用于管理青光眼的新生物标志物。