Dl. Jones et al., ALUMINUM INDUCES A DECREASE IN CYTOSOLIC CALCIUM-CONCENTRATION IN BY-2 TOBACCO CELL-CULTURES, Plant physiology, 116(1), 1998, pp. 81-89
Al toxicity is a major problem that limits crop productivity on acid s
oils. It has been suggested that Al toxicity is linked to changes in c
ellular Ca homeostasis and the blockage of plasma membrane Ca2+-permea
ble channels. BY-2 suspension-cultured cells of tobacco (Nicotiana tab
acum L.) exhibit rapid cell expansion that is sensitive to Al. Therefo
re, the effect of Al on changes in cytoplasmic free Ca concentration (
[Ca2+](cyt)) was followed in BY-2 cells to assess whether Al perturbed
cellular Ca homeostasis. Al exposure resulted in a prolonged reductio
n in [Ca2+](cyt) and inhibition of growth that was similar to the effe
ct of the Ca2+ channel blocker La3+ and the Ca2+ chelator ethyleneglyc
ol-bis(beta-aminoethyl ether)-N,N'-tetraacetic acid. The Ca2+ channel
blockers verapamil and nifedipine did not induce a decrease in [Ca2+](
cyt) in these cells and also failed to inhibit growth. Al and La3+, bu
t not verapamil or nifedipine, reduced the rate of Mn2+ quenching of I
ndo-1 fluorescence, which is consistent with the blockage of Ca2+- and
Mn2+-permeable channels. These results suggest that Al may act to blo
ck Ca2+ channels at the plasma membrane of plant cells and this action
may play a crucial role in the phytotoxic activity of the Al ion.