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空间组学揭示的心肌缺血/再灌注中的蛋白质改变

Protein Alterations in Cardiac Ischemia/Reperfusion Revealed by Spatial-Omics.

机构信息

Maastricht MultiModal Molecular Imaging (M4i) Institute, Division of Imaging Mass Spectrometry, Maastricht University, Universiteitssingel 50, 6229 ER Maastricht, The Netherlands.

Central Diagnostic Laboratory, Maastricht University Medical Center, P.O. Box 5800, 6202 AZ Maastricht, The Netherlands.

出版信息

Int J Mol Sci. 2022 Nov 10;23(22):13847. doi: 10.3390/ijms232213847.

Abstract

Myocardial infarction is the most common cause of death worldwide. An understanding of the alterations in protein pathways is needed in order to develop strategies that minimize myocardial damage. To identify the protein signature of cardiac ischemia/reperfusion (I/R) injury in rats, we combined, for the first time, protein matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) and label-free proteomics on the same tissue section placed on a conductive slide. Wistar rats were subjected to I/R surgery and sacrificed after 24 h. Protein MALDI-MSI data revealed ischemia specific regions, and distinct profiles for the infarct core and border. Firstly, the infarct core, compared to histologically unaffected tissue, showed a significant downregulation of cardiac biomarkers, while an upregulation was seen for coagulation and immune response proteins. Interestingly, within the infarct tissue, alterations in the cytoskeleton reorganization and inflammation were found. This work demonstrates that a single tissue section can be used for protein-based spatial-omics, combining MALDI-MSI and label-free proteomics. Our workflow offers a new methodology to investigate the mechanisms of cardiac I/R injury at the protein level for new strategies to minimize damage after MI.

摘要

心肌梗死是全球最常见的死亡原因。为了制定最大限度减少心肌损伤的策略,需要了解蛋白质途径的改变。为了确定大鼠心脏缺血/再灌注(I/R)损伤的蛋白质特征,我们首次将蛋白质基质辅助激光解吸/电离质谱成像(MALDI-MSI)和无标记蛋白质组学结合在放置在导电载玻片上的同一组织切片上。Wistar 大鼠接受 I/R 手术,24 小时后处死。蛋白质 MALDI-MSI 数据显示出缺血特异性区域,以及梗塞核心和边界的不同特征。首先,与组织学上未受影响的组织相比,梗塞核心显著下调了心脏生物标志物,而凝血和免疫反应蛋白则上调。有趣的是,在梗塞组织中,发现细胞骨架重组和炎症的改变。这项工作表明,单个组织切片可用于基于蛋白质的空间组学,结合 MALDI-MSI 和无标记蛋白质组学。我们的工作流程为在蛋白质水平上研究心脏 I/R 损伤的机制提供了一种新的方法,以制定新的策略来最大限度地减少 MI 后的损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ff5/9692276/72354f3337ac/ijms-23-13847-g001.jpg

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