In situ mass spectrometry of autoimmune liver diseases

被引:11
|
作者
Bowlus, Christopher L. [1 ]
Seeley, Erin H. [2 ]
Roder, Joanna [3 ]
Grigorieva, Julia [3 ]
Roder, Heinrich [3 ]
Caprioli, Richard M. [2 ]
Gershwin, M. Eric [4 ]
机构
[1] Univ Calif Davis, Div Gastroenterol & Hepatol, Davis, CA 95616 USA
[2] Vanderbilt Univ, Sch Med, Mass Spectrometry Res Ctr, Nashville, TN 37212 USA
[3] Biodesix, Steamboat Springs, CO USA
[4] Univ Calif Davis, Div Clin Immunol Allergy & Rheumatol, Davis, CA 95616 USA
关键词
autoimmune hepatitis; mass spectrometry; primary biliary cirrhosis; primary sclerosing cholangitis; PRIMARY BILIARY-CIRRHOSIS; GENE-EXPRESSION PROFILES; TISSUE-SECTIONS; BREAST-CANCER; LUNG-CANCER; MALDI-MS; HEPATITIS; PROTEINS; CELLS;
D O I
10.1038/cmi.2010.72
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Primary biliary cirrhosis (PBC), primary sclerosing cholangitis (PSC) and autoimmune hepatitis (AIH) are the major forms of autoimmune liver diseases each characterized by the destruction of a specific liver cell type and the presence of differing auto-antibodies. We took a proteomic approach utilizing in situ matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS) to obtain profiles directly from liver samples of patients with PBC, PSC, AIH and controls. The ability to precisely localize the region for acquisition of MALDI MS allowed us to obtain profiles from bile ducts, inflammatory infiltrates and hepatocytes from each biopsy sample. Analysis tools developed to identify peaks and compare peaks across diseases and cell types were used to develop models to classify the samples. Using an initial set of testing samples from PBC patients and controls, we identified unique peaks present in bile ducts, inflammatory infiltrates and hepatocytes that could classify samples in a validation cohort with 88-91% accuracy. Interestingly, profiles of PSC and AIH did not differ significantly from PBC. Identification of proteins in these peaks may represent novel autoantigens or effector molecules. These findings illustrate the potential of a proteomic approach to autoimmune diseases with in situ MALDI MS. © 2011 CSI and USTC. All rights reserved.
引用
收藏
页码:237 / 242
页数:6
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