TY - JOUR
T1 - Mechanism of blue-light-induced plasma-membrane depolarization in etiolated cucumber hypocotyls
AU - Spalding, Edgar P.
AU - Cosgrove, Daniel J.
PY - 1992/9
Y1 - 1992/9
N2 - A large, transient depolarization of the plasma membrane precedes the rapid blue-light (BL)-induced growth suppression in etiolated seedlings of Cucumis sativus L. The mechanism of this voltage transient was investigated by applying inhibitors of ion channels and the plasma-membrane H+-ATPase, by manipulating extracellular ion concentrations, and by measuring cell input resistance and ATP levels. The depolarizing phase was not affected by Ca2+-channel blockers (verapamil, La3+) or by reducing extracellular free Ca2+ by treatment with ethylene glycol-bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid (EGTA). However, these treatments did reduce the rate of repolarization, indicating an inward movement of Ca2+ is involved. No effects of the K+-channel blocker tetraethylammonium (TEA+) were detected. Vanadate and KCN, used to inhibit the H+-ATPase, reduced or completely inhibited the BL-induced depolarization. Levels of ATP increased by 11-26% after 1-2 min of BL. Input resistance of trichome cells, measured with double-barreled microelectrodes, remained constant during the onset of the depolarization but decreased as the membrane voltage became more positive than -90 mV. The results indicate that the depolarization mechanism initially involves inactivation of the H+-ATPase with subsequent transient activation of one or more types of ion channels.
AB - A large, transient depolarization of the plasma membrane precedes the rapid blue-light (BL)-induced growth suppression in etiolated seedlings of Cucumis sativus L. The mechanism of this voltage transient was investigated by applying inhibitors of ion channels and the plasma-membrane H+-ATPase, by manipulating extracellular ion concentrations, and by measuring cell input resistance and ATP levels. The depolarizing phase was not affected by Ca2+-channel blockers (verapamil, La3+) or by reducing extracellular free Ca2+ by treatment with ethylene glycol-bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid (EGTA). However, these treatments did reduce the rate of repolarization, indicating an inward movement of Ca2+ is involved. No effects of the K+-channel blocker tetraethylammonium (TEA+) were detected. Vanadate and KCN, used to inhibit the H+-ATPase, reduced or completely inhibited the BL-induced depolarization. Levels of ATP increased by 11-26% after 1-2 min of BL. Input resistance of trichome cells, measured with double-barreled microelectrodes, remained constant during the onset of the depolarization but decreased as the membrane voltage became more positive than -90 mV. The results indicate that the depolarization mechanism initially involves inactivation of the H+-ATPase with subsequent transient activation of one or more types of ion channels.
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U2 - 10.1007/BF00216814
DO - 10.1007/BF00216814
M3 - Article
C2 - 11540069
AN - SCOPUS:0026928672
SN - 0032-0935
VL - 188
SP - 199
EP - 205
JO - Planta
JF - Planta
IS - 2
ER -