1. Academic Validation
  2. A proteomic approach for the identification of immunotoxic properties of Tulipalin A

A proteomic approach for the identification of immunotoxic properties of Tulipalin A

  • Proteomics. 2016 Dec;16(23):2997-3008. doi: 10.1002/pmic.201600130.
Paula Zwicker 1 Nadin Schultze 1 Sarah Niehs 2 Karen Methling 2 Martina Wurster 2 Dirk Albrecht 3 Jörg Bernhardt 3 Gerhild Wachlin 3 Michael Lalk 2 Ulrike Lindequist 1 Beate Haertel 1
Affiliations

Affiliations

  • 1 Institute of Pharmacy, Pharmaceutical Biology, Ernst-Moritz-Arndt-University, Greifswald, Germany.
  • 2 Institute of Biochemistry, Biochemistry of Metabolism/Metabolomics, Ernst-Moritz-Arndt-University, Greifswald, Germany.
  • 3 Institute of Microbiology, Microbial Physiology and Molecular Biology, Ernst-Moritz-Arndt-University, Greifswald, Germany.
Abstract

The immune system is permanently exposed to several environmental influences that can have adverse effects on immune cells or organs leading to immunosuppression or inappropriate immunostimulation, called direct immunotoxicity. The natural compound Tulipalin A (TUPA), a lactone with α-methylene-γ-butyrolactone moiety, can influence the immune system and lead to allergic contact dermatitis. This in vitro study focused on effects of TUPA using two immune cell lines (Jurkat T cells and THP-1 monocytes). To evaluate the immunotoxic potential of the compound, a proteomic approach applying 2D gel electrophoresis and MALDI-TOF/TOF-MS in combination with metabolomic analysis was used after exposure of the cells to IC10 of TUPA. THP-1 cells showed a strong robustness to TUPA treatment since only five proteins were altered. In contrast, in Jurkat T cells an increase in the abundance of 66 proteins and a decrease of six proteins was determined. These intracellular proteins were mapped to biological processes. Especially an accumulation of chaperones and an influence on the purine synthesis were observed. The changes in purine synthesis were confirmed by metabolomic analysis. In conclusion, the data indicate possible target processes of low doses of TUPA in Jurkat T cells and provides knowledge of how TUPA affects the functionality of immune cells.

Keywords

Cell biology; Immunotoxicity; Metabolomics; OMICS; Toxicoproteomics; Tulipalin A.

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