淀粉样变性
淀粉样蛋白(真菌学)
病理
马尔迪成像
激光捕获显微切割
单克隆
淀粉样变性
免疫球蛋白轻链
医学
化学
基质辅助激光解吸/电离
单克隆抗体
免疫学
生物化学
抗体
有机化学
解吸
吸附
基因表达
基因
作者
Greta Bindi,Andrew Smith,Glenda Oliveira,Albino Eccher,Simona Vatrano,Federico Alberici,Giorgio Cazzaniga,Stefania Galimberti,Giulia Capitoli,Fulvio Magni,Fabio Pagni,Vincenzo L’Imperio
标识
DOI:10.1136/jcp-2023-208790
摘要
Aims Identification and characterisation of monoclonal gammopathies of renal significance (MGRS) is critical for therapeutic purposes. Amyloidosis represents one of the most common forms of MGRS, and renal biopsy remains the gold standard for their classification, although mass spectrometry has shown greater sensitivity in this area. Methods In the present study, a new in situ proteomic technique, matrix-assisted laser desorption/ionisation mass spectrometry imaging (MALDI-MSI), is investigated as an alternative to conventional laser capture microdissection MS for the characterisation of amyloids. MALDI-MSI was performed on 16 cases (3 lambda light chain amyloidosis (AL), 3 AL kappa, 3 serum amyloid A amyloidosis (SAA), 2 lambda light chain deposition disease (LCDD), 2 challenging amyloid cases and 3 controls). Analysis began with regions of interest labelled by the pathologist, and then automatic segmentation was performed. Results MALDI-MSI correctly identified and typed cases with known amyloid type (AL kappa, AL lambda and SAA). A ‘restricted fingerprint’ for amyloid detection composed of apolipoprotein E, serum amyloid protein and apolipoprotein A1 showed the best automatic segmentation performance (area under the curve >0.7). Conclusions MALDI-MSI correctly assigned minimal/challenging cases of amyloidosis to the correct type (AL lambda) and identified lambda light chains in LCDD cases, highlighting the promising role of MALDI-MSI for amyloid typing.
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