Anti-apoptotic signaling by HGF in NIH 3T3 cells transfected
with WT-Met. (A) Cells were serum starved
overnight, and after treatment with UV irradiation, fresh serum-free
medium, supplemented with (Left) or without
(Right) HGF, was added to the cells. Cells were
incubated for another 24 h and harvested for evaluation of
apoptosis by Hoechst 33342 staining. Normal nuclei show faint
delicate chromatin staining, nuclei at the early stage of
apoptosis display increased condensation and brightness, and
nuclei at the late stage of apoptosis exhibit chromatin
condensation and nuclear fragmentation. (B)
Apoptotic cells with characteristic chromatin condensation and
nuclear fragmentation were counted and expressed as a percentage of
the total cell number. Bar = mean ± SD of three
independent experiments. *, P < 0.01.