Abstract

The chemosensory transient receptor potential ankyrin 1 (TRPA1) ion channel perceives different sensory stimuli. It also interacts with reactive exogenous compounds including the chemical warfare agent sulfur mustard (SM). Activation of TRPA1 by SM results in elevation of intracellular calcium levels but the cellular consequences are not understood so far. In the present study we analyzed SM-induced and TRPA1-mediated effects in human TRPA1-overexpressing HEK cells (HEKA1) and human lung epithelial cells (A549) that endogenously exhibit TRPA1. The specific TRPA1 inhibitor AP18 was used to distinguish between SM-induced and TRPA1-mediated or TRPA1-independent effects. Cells were exposed to 600 µM SM and proteome changes were investigated 24 h afterwards by 2D gel electrophoresis. Protein spots with differential staining levels were analyzed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and nano liquid chromatography electrospray ionization tandem mass spectrometry. Results were verified by RT-qPCR experiments in both HEKA1 or A549 cells. Heat shock 70 kDa protein 6 (HSPA6) was identified as an SM-induced and TRPA1-mediated protein. AP18 pre-treatment diminished the up-regulation. RT-qPCR measurements verified these results and further revealed a time-dependent regulation. Our results demonstrate that SM-mediated activation of TRPA1 influences the protein expression and confirm the important role of TRPA1 ion channels in the molecular toxicology of SM.

Highlights

  • The chemical warfare agent sulfur mustard (SM) causes severe damage to the skin, eyes, and the respiratory system [1,2]

  • Analysis of HEKA1 cells exposed to SM and investigated after 24 h revealed differential detection of 22 protein spots compared to the control group (Figure 1A) in CBB-stained 2D gels

  • Dependency on transient receptor potential ankyrin 1 cation channels (TRPA1) was proven as pre-incubation with AP18 prevented SM-induced effects

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Summary

Introduction

The chemical warfare agent sulfur mustard (SM) causes severe damage to the skin, eyes, and the respiratory system [1,2]. Stenger et al demonstrated that the alkylating substances CEES (2-chloroethyl-ethyl sulfide, a mono-functional SM analogue) and SM activate transient receptor potential ankyrin 1 cation channels (TRPA1) in vitro, thereby affecting cell viability [4]

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