Figure 7
Actin reorganization in metallothionein-stimulated cells. Jurkat T cells were treated with metallothionein at 2 μM and then harvested and fixed at various times after stimulation. Cells were stained with rhodamine phalloidin and F-actin fluorescence quantified using a plate fluorimeter. (RFU = relative fluorescent units). Values reported represent the average of 3 replicates ± standard deviation. *** represents significant difference from the medium alone control (p < 0.001). This data is representative of 3 independent experiments.