TY - JOUR
T1 - Proteome analysis of diseased joints from mice suffering from collagen-induced arthritis
AU - Lorenz, Peter
AU - Bantscheff, Marcus
AU - Ibrahim, Saleh M.
AU - Thiesen, Hans Jürgen
AU - Glocker, Michael O.
N1 - Funding Information:
The authors would like to thank I. Klamfuss and M. Sieb for excellent technical assistance, Dr. H. Kreutzer and Prof. Dr. H. Nizze for histopathological analysis, and all the colleagues, particularly Dr. S. Mikkat and Dr. B. Ringel, at the Proteome Center Rostock for their support. This work was supported by grants from the German Federal Ministry for Research (BMBF, FKZ: 01GG9831) to HJT and to MOG, the Deutsche For-schungsgemeinschaft (DFG) and EU (QLRT-2000-01407) to SMI and the FORUN program of the Medical Faculty of the University of Rostock to PL and SMI.
PY - 2003
Y1 - 2003
N2 - Strains of mice that are susceptible to autoimmunity have provided experimental models to analyze the molecular basis for the complex multifactorial inheritance of human autoimmune disease. In this study proteins associated with collagen-induced arthritis (CIA) in mice were experimentally identified using a global proteomics approach. Two-dimensional gels of proteins from inflamed and non-inflamed joints showed a distinguished protein profile visualizing about 530 Coomassie-stained protein spots in the pH 4-7 range. A total of 76 spots were identified by peptide mass fingerprinting with good confidence. They included proteins of cytoskeletal origin, chaperones, enzymes and also some signal transduction molecules. Comparison to gels from non-inflamed paws pointed to proteins that were differentially expressed between the control and diseased state. Ferritin light chain and antioxidant protein 2 were slightly more abundant, lymphoid enhancer binding factor 1 slightly, but significantly, less abundant in inflamed paws. Fourteen of the identified proteins were the products of genes that had increased transcript levels in the diseased state. However, on the protein level no significant differences were found in comparison to the controls. This study provides us with the framework for more detailed approaches to understanding the complex disease arthritis that go beyond global proteomics.
AB - Strains of mice that are susceptible to autoimmunity have provided experimental models to analyze the molecular basis for the complex multifactorial inheritance of human autoimmune disease. In this study proteins associated with collagen-induced arthritis (CIA) in mice were experimentally identified using a global proteomics approach. Two-dimensional gels of proteins from inflamed and non-inflamed joints showed a distinguished protein profile visualizing about 530 Coomassie-stained protein spots in the pH 4-7 range. A total of 76 spots were identified by peptide mass fingerprinting with good confidence. They included proteins of cytoskeletal origin, chaperones, enzymes and also some signal transduction molecules. Comparison to gels from non-inflamed paws pointed to proteins that were differentially expressed between the control and diseased state. Ferritin light chain and antioxidant protein 2 were slightly more abundant, lymphoid enhancer binding factor 1 slightly, but significantly, less abundant in inflamed paws. Fourteen of the identified proteins were the products of genes that had increased transcript levels in the diseased state. However, on the protein level no significant differences were found in comparison to the controls. This study provides us with the framework for more detailed approaches to understanding the complex disease arthritis that go beyond global proteomics.
UR - http://www.scopus.com/inward/record.url?scp=0346097946&partnerID=8YFLogxK
U2 - 10.1515/CCLM.2003.246
DO - 10.1515/CCLM.2003.246
M3 - Journal articles
C2 - 14708887
AN - SCOPUS:0346097946
SN - 1434-6621
VL - 41
SP - 1622
EP - 1632
JO - Clinical Chemistry and Laboratory Medicine
JF - Clinical Chemistry and Laboratory Medicine
IS - 12
ER -