Skip to main content
. 2001 Jan 9;98(2):473–478. doi: 10.1073/pnas.011417098

Figure 2.

Figure 2

(A) Western analysis of p21Waf1 expression in α-particle-irradiated AG1522 human fibroblasts in the presence or absence of lindane (40 μM), DDT, or dieldrin. At 10 cGy, by which about 50–60% of the cells' nuclei are traversed by an α-particle track, p21Waf1 is induced in the presence or absence of the inhibitors. At 1 cGy, by which only 7% of the cells in the culture would have their nuclei traversed by an α-particle, p21Waf1 induction is not detected in the presence of any of the inhibitors. (B). In situ immunofluorescence detection of p21Waf1 expression in nonirradiated lindane-treated (40 μM), and irradiated AG1522 cultures exposed to 0.3 cGy α-particles in the presence or absence of lindane. The absence of induced aggregates of cells in the irradiated and lindane-pretreated cultures indicates that GJIC contributes to the bystander response. (C) In situ immunofluorescence detection of p21Waf1 expression in AG1522 cultures exposed to 10 cGy in the presence or absence of lindane.