Integrating mass spectrometry imaging and data-driven segmentation for spatial metabolic mapping of diabetic eye disease.

IF 8.9
Journal of pharmaceutical analysis Pub Date : 2026-08-01 Epub Date: 2026-03-02 DOI:10.1016/j.jpha.2026.101596
Shuohan Cheng, Shuo Wang, Tianfang Lan, Hongtao Jin, Zhi Zhou, Zhonghua Wang, Zeper Abliz
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Abstract

Diabetic eye disease (DED) is a leading cause of vision impairment worldwide, yet the molecular mechanisms underlying its progression remain incompletely understood. In this study, we applied a dual-platform spatial metabolomics strategy integrating air flow-assisted desorption electrospray ionization mass spectrometry imaging (AFADESI-MSI) and matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI-MSI) to characterize spatial metabolic alterations in the eyes of diabetic rats. Data-driven segmentation of retinal micro-regions using SCiLS Lab software enabled fine-scale mapping of metabolic heterogeneity. Physiological, biochemical, and histopathological analyses were combined with spatial metabolite mapping to construct a metabolic atlas and evaluate the regulatory effects of ferulic acid. We established a comprehensive spatial metabolome atlas of the rat eye, identifying 135 annotated metabolites and revealing significant region-specific metabolic heterogeneity. Unsupervised k-means clustering was further applied to the high-resolution MALDI-MSI data, successfully delineating distinct functional micro-regions of the retina solely based on endogenous metabolic profiles, demonstrating the power of data-driven tissue segmentation. In diabetic eyes, 39 metabolites were significantly dysregulated, involving amino acid, glucose, lipid, and redox metabolism. Notably, lysine, arginine, carnitine, and glutathione (GSH) were depleted, while glucose-6-phosphate (G6P), glycerol-3-phosphate (G3P), and pro-inflammatory lipids were elevated, highlighting profound metabolic reprogramming across ocular compartments. Ferulic acid treatment restored nine key metabolites, alleviated oxidative stress, normalized lipid and glucose metabolism, and improved retinal structural integrity in a dose-dependent manner. This study shows that integrating mass spectrometry imaging with data-driven tissue segmentation reveals spatial metabolic reprogramming in DED and highlights ferulic acid as a promising therapeutic candidate.

整合质谱成像和数据驱动分割用于糖尿病眼病的空间代谢制图。
糖尿病性眼病(DED)是世界范围内视力损害的主要原因,但其发展的分子机制仍不完全清楚。在这项研究中,我们采用双平台空间代谢组学策略,结合气流辅助解吸电喷雾质谱成像(AFADESI-MSI)和基质辅助激光解吸电离质谱成像(MALDI-MSI)来表征糖尿病大鼠眼睛的空间代谢变化。使用SCiLS Lab软件对视网膜微区域进行数据驱动的分割,实现了代谢异质性的精细映射。将生理、生化和组织病理学分析与空间代谢物图谱相结合,构建代谢图谱并评估阿魏酸的调节作用。我们建立了大鼠眼睛的综合空间代谢组图谱,鉴定了135种带注释的代谢物,并揭示了显著的区域特异性代谢异质性。无监督k-means聚类进一步应用于高分辨率MALDI-MSI数据,仅基于内源性代谢谱就成功描绘了视网膜的不同功能微区域,证明了数据驱动的组织分割的力量。在糖尿病眼睛中,39种代谢物明显失调,涉及氨基酸、葡萄糖、脂质和氧化还原代谢。值得注意的是,赖氨酸、精氨酸、肉碱和谷胱甘肽(GSH)被消耗,而葡萄糖-6-磷酸(G6P)、甘油-3-磷酸(G3P)和促炎脂质升高,突出了眼部间室深刻的代谢重编程。阿魏酸治疗恢复了九种关键代谢物,减轻了氧化应激,使脂质和葡萄糖代谢正常化,并以剂量依赖的方式改善了视网膜结构的完整性。该研究表明,将质谱成像与数据驱动的组织分割相结合,揭示了DED的空间代谢重编程,并强调阿魏酸是一种有前景的治疗候选药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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