In situ mass spectrometry of autoimmune liver diseases

被引:13
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
相关论文
共 20 条
[1]   Selective profiling of proteins in lung cancer cells from fine-needle aspirates by matrix-assisted laser desorption ionization time-of-flight mass spectrometry [J].
Amann, Joseph M. ;
Chaurand, Pierre ;
Gonzalez, Adriana ;
Mobley, James A. ;
Massion, Pierre P. ;
Carbone, David P. ;
Caprioli, Richard M. .
CLINICAL CANCER RESEARCH, 2006, 12 (17) :5142-5150
[2]   A comparison of selected mRNA and protein abundances in human liver [J].
Anderson, L ;
Seilhamer, J .
ELECTROPHORESIS, 1997, 18 (3-4) :533-537
[3]  
[Anonymous], 2003, Statistical pattern recognition
[4]   Gene expression by PBMC in primary sclerosing cholangitis: Evidence for dysregulation of immune mediated genes [J].
Aoki, Christopher A. ;
Dawson, Kevin ;
Kenny, Thomas P. ;
Gershwin, M. Eric ;
Bowlus, Christopher L. .
CLINICAL & DEVELOPMENTAL IMMUNOLOGY, 2006, 13 (2-4) :265-271
[5]   The immunobiology of primary sclerosing cholangitis [J].
Aron, Jonathan H. ;
Bowlus, Christopher L. .
SEMINARS IN IMMUNOPATHOLOGY, 2009, 31 (03) :383-397
[6]   Identification of Markers of Taxane Sensitivity Using Proteomic and Genomic Analyses of Breast Tumors from Patients Receiving Neoadjuvant Paclitaxel and Radiation [J].
Bauer, Joshua A. ;
Chakravarthy, A. Bapsi ;
Rosenbluth, Jennifer M. ;
Mi, Deming ;
Seeley, Erin H. ;
Granja-Ingram, Nara De Matos ;
Olivares, Maria G. ;
Kelley, Mark C. ;
Mayer, Ingrid A. ;
Meszoely, Ingrid M. ;
Means-Powell, Julie A. ;
Johnson, Kimberly N. ;
Tsai, Chiaojung Jillian ;
Ayers, Gregory D. ;
Sanders, Melinda E. ;
Schneider, Robert J. ;
Formenti, Silvia C. ;
Caprioli, Richard M. ;
Pietenpol, Jennifer A. .
CLINICAL CANCER RESEARCH, 2010, 16 (02) :681-690
[7]   New developments in profiling and imaging of proteins from tissue sections by MALDI mass spectrometry [J].
Chaurand, Pierre ;
Norris, Jeremy L. ;
Cornett, D. Shannon ;
Mobley, James A. ;
Caprioli, Richard M. .
JOURNAL OF PROTEOME RESEARCH, 2006, 5 (11) :2889-2900
[8]   Molecular imaging of thin mammalian tissue sections by mass spectrometry [J].
Chaurand, Pierre ;
Cornett, D. Shannon ;
Caprioli, Richard M. .
CURRENT OPINION IN BIOTECHNOLOGY, 2006, 17 (04) :431-436
[9]   Gene expression profiling of early primary biliary cirrhosis: possible insights into the mechanism of action of ursodeoxycholic acid [J].
Chen, Limin ;
Borozan, Ivan ;
Milkiewicz, Piotr ;
Sun, Jing ;
Meng, Xiangbin ;
Coltescu, Catalina ;
Edwards, Aled M. ;
Ostrowski, Mario A. ;
Guindi, Maha ;
Heathcote, Elizabeth J. ;
McGilvray, Ian D. .
LIVER INTERNATIONAL, 2008, 28 (07) :997-1010
[10]   A novel histology-directed strategy for MALDI-MS tissue profiling that improves throughput and cellular specificity in human breast cancer [J].
Cornett, Dale S. ;
Mobley, James A. ;
Dias, Eduardo C. ;
Andersson, Malin ;
Arteaga, Carlos L. ;
Sanders, Melinda E. ;
Caprioli, Richard M. .
MOLECULAR & CELLULAR PROTEOMICS, 2006, 5 (10) :1975-1983