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. 2018 May 28;37(13):e98354. doi: 10.15252/embj.201798354

Figure 6. Cytotoxicity of HRP‐dependent DAB polymerization occurring at the Golgi apparatus.

Figure 6

  • A, B
    Two clones of U2OS cells that stably express HRP were stained for the GA marker GALT (A) showing extensive colocalization as determined by the Pearson correlation coefficient (B). Scale bar: 10 μm.
  • C–E
    Cytotoxicity and DAB polymerization observed in U2OS‐GA‐HRP cells after treatment with DAB/H2O2 for 24 h at 37°C (C). Percentage of cells with DAB aggregates (D) and quantification of dead cells (PI+ cells) (E). DAB precipitates were observed by transmitted light microscopy, whereas cell viability was assessed by fluorescence microscopy upon double staining with PI and Hoechst. Scale bar: 20 μm.
Data information: Bars indicate means ± SD of triplicates of one representative experiment out of two repeats. Asterisks indicate significant differences with respect to untreated cells, whereas hashes indicate significant differences between WT cells and GA‐HRP clones, ***P < 0.001; ### P < 0.001 (two‐way ANOVA).