Aluminum-induced cell death was investigated in root-tip cells of barley (H
ordeum vulgare). The growth of roots in 0.1-50 mM Al treatments was inhibit
ed after 8 h treatments, and could not be recovered after 24 h recovery cul
ture without Al. Viable detection with fluorescein diacetate-propidium iodi
de (FDA-PI) staining shows that most of the root-tip cells have lost viabil
ity. These results suggest that the irreversible inhibition of root growth
after 8 h Al treatments or 24 h recovery culture is mainly caused by cell d
eath. DNA ladders occurred in root tips only after 8 h Al treatments (0.1-1
.0 mM), but no apoptotic bodies in root tips were observed. Thus, the cell
death caused by Al stress is likely to be Al-induced programmed cell death
(PCD). The reactive oxygen species (ROS) in root-tip cells measured by ultr
aweak luminescence indicated that the oxidation status in root-tip cells ba
sically ceased after exposure to 10-50 mM Al for 24 h, but was very violent
in the root-tip cells treated with 0.1-1.0 mM for 24 h. Exposure to 0.1-1.
0 mM Al for 3-12 h led to ROS burst. Therefore, our results suggest that 0.
1-1.0 mM Al treatments for 8 h induce cell death (Al-induced PCD) possibly
via a ROS-activated signal transduction pathway, whereas 10-50 mM Al treatm
ents may cause necrosis in the root-tip cells. These results have an import
ant role for further studies on the mechanism of Al toxicity in plants. (C)
2001 Elsevier Science B.V. All rights reserved.