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Proteome analysis of diseased joints from mice suffering from collagen-induced arthritis

Peter Lorenz, Marcus Bantscheff, Saleh M. Ibrahim, Hans Jürgen Thiesen, Michael O. Glocker*

*Korrespondierende/r Autor/-in für diese Arbeit

Abstract

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.

OriginalspracheEnglisch
ZeitschriftClinical Chemistry and Laboratory Medicine
Jahrgang41
Ausgabenummer12
Seiten (von - bis)1622-1632
Seitenumfang11
ISSN1434-6621
DOIs
PublikationsstatusVeröffentlicht - 2003

Fördermittel

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.

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

  1. SDG 3 – Gesundheit und Wohlergehen
    SDG 3 – Gesundheit und Wohlergehen

Strategische Forschungsbereiche und Zentren

  • Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)

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