Visualization of cyclooxygenase-2 using a 2,3-diarylsubstituted indole-based inhibitor and confocal laser induced cryofluorescence microscopy at 20K in melanoma cells in vitro

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Christoph Tondera - , Faculty of Chemistry and Food Chemistry, Helmholtz-Zentrum Dresden-Rossendorf (Author)
  • Markus Laube - , Helmholtz-Zentrum Dresden-Rossendorf, TUD Dresden University of Technology (Author)
  • Christin Wimmer - , Faculty of Chemistry and Food Chemistry, Helmholtz-Zentrum Dresden-Rossendorf (Author)
  • Torsten Kniess - , Helmholtz-Zentrum Dresden-Rossendorf (Author)
  • Birgit Mosch - , Helmholtz-Zentrum Dresden-Rossendorf (Author)
  • Kay Großmann - , Helmholtz-Zentrum Dresden-Rossendorf (Author)
  • Jens Pietzsch - , Helmholtz-Zentrum Dresden-Rossendorf, TUD Dresden University of Technology (Author)

Abstract

This study aimed at visualization of cyclooxygenase-2 (COX-2) protein expression in melanoma cells by confocal laser induced cryofluorescence microscopy using 4-(3-(4-methoxyphenyl)-1H-indol-2-yl)benzene-sulfonamide (C1) representative for a novel class of autofluorescent 2,3-diarylsubstituted indole-based selective COX-2 inhibitors.COX-2 expression was measured in human melanoma cell lines A2058 and MelJuso by immunocytochemistry and immunoblotting. Cellular uptake experiments using varying C1 concentrations down to 0.1. nM (with/without molar excess of celecoxib as control) were performed at 37°C. Cryofluorescence microscopy was conducted at 20. K.COX-2 protein expression was successfully visualized by C1 in A2058 cells. COX-2-negative MelJuso cells showed no specific accumulation of C1. Control experiments using celecoxib and, additionally, implemented fluorescence spectroscopy confirmed specificity of both cellular uptake and intracellular association of C1.Cryofluorescence microscopy in combination with spectroscopy allowed for visualization of COX-2 protein expression in melanoma cells in vitro using a selective COX-2 inhibitor at very low concentrations. © 2012 Elsevier Inc.

Details

Original languageEnglish
Pages (from-to)301-306
Number of pages6
JournalBiochemical and biophysical research communications
Volume430
Issue number1
Publication statusPublished - 4 Jan 2013
Peer-reviewedYes

External IDs

PubMed 23146632
Scopus 84872398584

Keywords

Keywords

  • Coxibs, Fluorescence imaging, Pigment cells, Tumor inflammogenesis