Proteomic profiling in an animal model of acute pancreatitis

被引:25
作者
Fetaud, Vanessa [2 ]
Frossard, Jean-Louis [3 ]
Farina, Annarita [2 ]
Pastot, Catherine M. [3 ]
Buehler, Leo [4 ]
Dumonceau, Jean-Marc [3 ]
Hadengue, Antoine [3 ]
Hochstrasser, Denis F. [2 ]
Lescuyer, Pierre [1 ,2 ]
机构
[1] Univ Hosp Geneva, SML DMGL, Dept Genet & Lab Med, Clin Prote Lab, CH-1211 Geneva 14, Switzerland
[2] Geneva Fac Med, Dept Bioinformat & Struct Biol, Biomed Prote Res Grp, Geneva, Switzerland
[3] Univ Hosp Geneva, Div Gastroenterol & Hepatol, CH-1211 Geneva, Switzerland
[4] Univ Hosp Geneva, Surg Res Unit, Dept Surg, CH-1211 Geneva 14, Switzerland
基金
瑞士国家科学基金会;
关键词
acute pancreatitis; apoptosis; biomarker; inflammation; oxidative stress;
D O I
10.1002/pmic.200800066
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Acute pancreatitis (AP) is an inflammatory disease of the pancreas, which evolves in approximately 20% of the patients to a severe illness associated with a high mortality rate. In this study, we performed a comparative proteomic analysis of pancreatic tissue extracts from rats with AP and healthy rodent controls in order to identify changes in protein expression related to the pathobiological processes of this disease. Pancreatic extracts from diseased and controls rats were analyzed by 2-DE and MS/MS. A total of 125 proteins were identified from both samples. Comparative analysis allowed the detection of 42 proteins or protein fragments differentially expressed between diseased and control pancreas, some of them being newly described in AP. Interestingly, these changes were representative of the main pathobiological pathways involved in this disease. We observed activation of digestive proteases and increased expression of various inflammatory markers, including several members of the a-macroglobulin family. We also detected changes related to oxidative and cell stress responses. Finally, we highlighted modifications of 14-3-3 proteins that could be related to apoptosis regulation. These results showed the interest of proteomic analysis to identify changes characterizing pancreatic tissue damage and, therefore, to highlight new potential biomarkers of AP.
引用
收藏
页码:3621 / 3631
页数:11
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