Skip to main content
. 2013 Apr 24;41(12):6109–6118. doi: 10.1093/nar/gkt304

Figure 1.

Figure 1.

Pan-nuclear H2AX phosphorylation after localized IR-induced DNA damage to the nucleus. Different types of cell lines were fixed 1 h after ion irradiation and immunostained for γH2AX (green) and DNA (ToPro-3, red). Cells were irradiated (IR) at low angle with gold (A–C) or xenon ions (E), or with 40 carbon ions in 1 spot at the microprobe (D). (F) Nuclei of confluent human fibroblasts were detected by Hoechst staining and marked for irradiation (red crosses) to target either the cytoplasm (top) or the nucleus (bottom). Cells were irradiated with one gold ion. The mean pan-nuclear γH2AX signal was measured in unirradiated cells (ctrl) and after irradiation of the cytoplasm (Cy) or the nucleus (Nu) (right) (number of analyzed cells: 327, 193 and 53). Scale bar: 20 µm. (G) Exemplary intensity profiles of the γH2AX (green) and DNA (red) signal (relative value) are shown for a human fibroblast hit by a gold ion at low angle (top) and an unirradiated nucleus (bottom) fixed at 1 h. Error bars denote SD (**P < 0.01, n.s. = not significant, using two-sided U-test).