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用于异质组织结构蛋白质组描绘的基质辅助激光解吸/电离成像技术

MALDI Imaging for Proteomic Painting of Heterogeneous Tissue Structures.

作者信息

Kriegsmann Jörg, Kriegsmann Mark, Kriegsmann Katharina, Longuespée Rémi, Deininger Sören-Oliver, Casadonte Rita

机构信息

Proteopath GmbH, Trier 54296, Germany.

MVZ for Histology, Cytology and Molecular Diagnostics, Trier 54296, Germany.

出版信息

Proteomics Clin Appl. 2019 Jan;13(1):e1800045. doi: 10.1002/prca.201800045. Epub 2018 Nov 30.

Abstract

PURPOSE

To present matrix-assisted laser desorption/ionization (MALDI) imaging as a powerful method to highlight various tissue compartments.

EXPERIMENTAL DESIGN

Formalin-fixed paraffin-embedded (FFPE) tissue of a uterine cervix, a pancreas, a duodenum, a teratoma, and a breast cancer tissue microarray (TMA) are analyzed by MALDI imaging and by immunohistochemistry (IHC). Peptide images are visualized and analyzed using FlexImaging and SCiLS Lab software. Different histological compartments are compared by hierarchical cluster analysis.

RESULTS

MALDI imaging highlights tissue compartments comparable to IHC. In cervical tissue, normal epithelium can be discerned from intraepithelial neoplasia. In pancreatic and duodenal tissues, m/z signals from lymph follicles, vessels, duodenal mucosa, normal pancreas, and smooth muscle structures can be visualized. In teratoma, specific m/z signals to discriminate squamous epithelium, sebaceous glands, and soft tissue are detected. Additionally, tumor tissue can be discerned from the surrounding stroma in small tissue cores of TMAs. Proteomic data acquisition of complex tissue compartments in FFPE tissue requires less than 1 h with recent mass spectrometers.

CONCLUSION AND CLINICAL RELEVANCE

The simultaneous characterization of morphological and proteomic features in the same tissue section adds proteomic information for histopathological diagnostics, which relies at present on conventional hematoxylin and eosin staining, histochemical, IHC and molecular methods.

摘要

目的

介绍基质辅助激光解吸/电离(MALDI)成像作为一种突出显示各种组织成分的强大方法。

实验设计

通过MALDI成像和免疫组织化学(IHC)分析子宫颈、胰腺、十二指肠、畸胎瘤和乳腺癌组织微阵列(TMA)的福尔马林固定石蜡包埋(FFPE)组织。使用FlexImaging和SCiLS Lab软件对肽图像进行可视化和分析。通过层次聚类分析比较不同的组织学成分。

结果

MALDI成像突出显示的组织成分与IHC相当。在宫颈组织中,可将正常上皮与上皮内瘤变区分开来。在胰腺和十二指肠组织中,可可视化来自淋巴滤泡、血管、十二指肠黏膜、正常胰腺和平滑肌结构的m/z信号。在畸胎瘤中,检测到用于区分鳞状上皮、皮脂腺和软组织的特定m/z信号。此外,在TMA的小组织芯中,可将肿瘤组织与周围基质区分开来。使用最新的质谱仪,获取FFPE组织中复杂组织成分的蛋白质组数据所需时间不到1小时。

结论及临床意义

在同一组织切片中同时表征形态学和蛋白质组学特征,为目前依赖传统苏木精和伊红染色、组织化学、IHC和分子方法的组织病理学诊断增加了蛋白质组学信息。

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