Metabolomic analysis of Shiga toxin 2a-induced injury in conditionally immortalized glomerular endothelial cells
Language English Country United States Media electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
31576432
DOI
10.1007/s11306-019-1594-2
PII: 10.1007/s11306-019-1594-2
Knihovny.cz E-resources
- Keywords
- Conditionally immortalized glomerular endothelial cells, Hemolytic uremic syndrome, Metabolomics, Shiga toxin,
- MeSH
- Endothelial Cells cytology drug effects metabolism MeSH
- Kidney Glomerulus cytology MeSH
- Cells, Cultured MeSH
- Humans MeSH
- Lipopolysaccharides MeSH
- Metabolomics * MeSH
- Multivariate Analysis MeSH
- Cell Count MeSH
- Shiga Toxin 2 metabolism pharmacology MeSH
- Cell Survival drug effects MeSH
- Inflammation chemically induced metabolism pathology MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Lipopolysaccharides MeSH
- Shiga Toxin 2 MeSH
INTRODUCTION: Shiga toxin 2a (Stx2a) induces hemolytic uremic syndrome (STEC HUS) by targeting glomerular endothelial cells (GEC). OBJECTIVES: We investigated in a metabolomic analysis the response of a conditionally immortalized, stable glomerular endothelial cell line (ciGEnC) to Stx2a stimulation as a cell culture model for STEC HUS. METHODS: CiGEnC were treated with tumor necrosis factor-(TNF)α, Stx2a or sequentially with TNFα and Stx2a. We performed a metabolomic high-throughput screening by lipid- or gas chromatography and subsequent mass spectrometry. Metabolite fold changes in stimulated ciGEnC compared to untreated cells were calculated. RESULTS: 320 metabolites were identified and investigated. In response to TNFα + Stx2a, there was a predominant increase in intracellular free fatty acids and amino acids. Furthermore, lipid- and protein derived pro-inflammatory mediators, oxidative stress and an augmented intracellular energy turnover were increased in ciGEnC. Levels of most biochemicals related to carbohydrate metabolism remained unchanged. CONCLUSION: Stimulation of ciGEnC with TNFα + Stx2a is associated with profound metabolic changes indicative of increased inflammation, oxidative stress and energy turnover.
Department of Pediatrics 1 University Children's Hospital Heidelberg 69120 Heidelberg Germany
Department of Pharmaceutical Sciences Bahá'í Institute of Higher Education Teheran Iran
Division of Functional Genome Analysis German Cancer Research Center 69120 Heidelberg Germany
Institute for Hygiene University of Münster 48149 Münster Germany
Learning and Research Southmead Hospital Bristol University of Bristol Bristol BS8 1TH UK
Metabolon Inc 617 Davis Drive Suite 400 Durham NC 27713 USA
The Principal's Office University of Edinburgh Edinburgh EH8 9YL UK
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