Metabolomics
In a disease state different proteins are newly synthesized while the expression of other proteins is repressed. However, not only the protein composition and levels are changed during a disease, there are also changes in metabolite concentrations. The usage of metabolic profiles in an “omics” setting is emerging since a few years. In a clinical setting it is used for improved diagnosis and for prediction of therapy outcome. In basic research it allows identification of pathways that are involved in or influenced by a certain (organismal) state. This will provide clues to diagnosis as well as to a deeper understanding of the disease itself.
Our group used NMR spectroscopy for metabolic investigations. We have determined metabolic changes in a mouse model of an inflammatory autoimmune skin disease [1] and identified a metabolic marker for cellular senescence in human fibroblasts [2] and skin melanocytes [3].
We participate with a project on metabolomics in the research training group GRK1727/2 "Modulation of Autoimmunity".
Literature
- Schönig S, Recke A, Hirose M, Ludwig R, Seeger K. Metabolite analysis distinguishes between mice with epidermolysis bullosa acquisita and healthy mice. Orphanet Journal of Rare Diseases 2013, 8(1):93. DOI: 10.1186/1750-1172-8-93
- Gey C, Seeger K. Metabolic changes during cellular senescence investigated by proton NMR-spectroscopy. Mech Ageing Dev 2013, 134(3-4): 130-138. DOI: 10.1016/j.mad.2013.02.002
- Windler C, Gey C, Seeger K.: Skin melanocytes and fibroblasts show different changes in choline metabolism during cellular senescence. Mech Ageing Dev 2017 164:82-90. DOI: 10.1016/j.mad.2017.05.001
review articles/book chapters
- Seeger K.: Metabolic changes in autoimmune diseases. In Curr. Drug Discov. Technol. 6 (2009), 256-261. DOI: 10.2174/157016309789869074
- Gey, C. and Seeger, K., 2017. Metabolic changes investigated by proton NMR spectroscopy in cells undergoing oncogene-induced senescence, in: Nikiforov, M.A. (Ed.), Oncogene-Induced Senescence: Methods and Protocols. Springer New York, New York, NY, pp. 155-163. DOI: 10.1007/978-1-4939-6670-7_15
Prof. Dr. Karsten Seeger
Gebäude 61,
Raum 323
Email: | karsten.seeger(at)uni-luebeck.de |
Phone: | +49 451 3101-3334 |