Skip to main content
. Author manuscript; available in PMC: 2018 Dec 1.
Published in final edited form as: Reprod Toxicol. 2017 Oct 3;74:181–188. doi: 10.1016/j.reprotox.2017.09.010

Fig. 5.

Fig. 5

Effects of AhR siRNA on the ITE-inhibited proliferation and viability of HUVECs and HUAECs as well as migration of HUAECs. Cells were treated with the vehicle control or transfected with the scrambled (ssiRNA) or AhR siRNA (siRNA) for 2 days. After transfection, cells were treated with ITE (1 μM) for 4 days for cell proliferation (A and B) and for cell viability (C and D), or for 2 days for cell migration (E) with a daily change of ITE, followed by the cell proliferation, viability, and migration assays. Data are expressed as means ± SEM% of the vehicle (Veh; n = 5–6) in the absence of ITE. One-way ANOVA was conducted followed by comparisons verse the respective Veh in the absence of ITE. *Differ from Veh in the absence of ITE (p < 0.05).