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脱落酸激活非选择性钙离子通透通道使保卫细胞胞质钙离子浓度反复升高。

Repetitive increases in cytosolic Ca2+ of guard cells by abscisic acid activation of nonselective Ca2+ permeable channels.

作者信息

Schroeder J I, Hagiwara S

机构信息

Department of Physiology, Jerry Lewis Neuromuscular Research Center, University of California, Los Angeles School of Medicine 90024.

出版信息

Proc Natl Acad Sci U S A. 1990 Dec;87(23):9305-9. doi: 10.1073/pnas.87.23.9305.

Abstract

Many signal-transduction processes in higher plant cells have been suggested to be triggered by signal-induced opening of Ca2+ channels in the plasma membrane. However, direct evidence for activation of plasma-membrane Ca2+ channels by physiological signals in higher plants has not yet been obtained. In this context, several lines of evidence suggest that Ca2+ flux into the cytosol of guard cells is a major factor in the induction of stomatal closing by abscisic acid (ABA). ABA closes stomatal pores, thereby reducing transpirational loss of water by plants under drought conditions. To directly investigate initial events in ABA-induced signal transduction in guard cells, we devised an experimental approach that allows simultaneous photometric measurements of cytosolic Ca2+ and patch-clamp recordings of ion currents across the plasma membrane of single Vicia faba guard cells. Using this approach, we found that the resting cytosolic Ca2+ concentration was 0.19 +/- 0.09 microM (n = 19). In responsive guard cells, external exposure to ABA produced transient repetitive increases in the cytosolic free Ca2+ concentration. These Ca2+ transients were accompanied by concomitantly occurring increases in an inward-directed ion current. Depolarization of the membrane terminated both repetitive elevations in cytosolic Ca2+ and inward-directed ion currents, suggesting that ABA-mediated Ca2+ transients were produced by passive influx of Ca2+ from the extracellular space through Ca2(+)-permeable channels. Detailed voltage-clamp measurements revealed that ABA-activated ion currents could be reversed by depolarizations more positive than -10 mV. Interestingly, reversal potentials of ABA-induced currents show that these currents are not highly Ca2(+)-selective, thereby permitting permeation of both Ca2+ and K+. These results provide direct evidence for ABA activation of Ca2(+)-permeable ion channels in the plasma membrane of guard cells. ABA-activated ion channels allow repetitive elevations in the cytosolic Ca2+ concentration, which, in turn, can modulate cellular responses promoting stomatal closure.

摘要

高等植物细胞中的许多信号转导过程被认为是由信号诱导质膜上Ca2+通道开放所触发的。然而,尚未获得高等植物中生理信号激活质膜Ca2+通道的直接证据。在此背景下,有几条证据表明,Ca2+流入保卫细胞的细胞质是脱落酸(ABA)诱导气孔关闭的主要因素。ABA关闭气孔孔道,从而减少干旱条件下植物的蒸腾失水。为了直接研究保卫细胞中ABA诱导的信号转导的初始事件,我们设计了一种实验方法,该方法允许同时对单个蚕豆保卫细胞质中的Ca2+进行光度测量,并对质膜上的离子电流进行膜片钳记录。使用这种方法,我们发现静息细胞质Ca2+浓度为0.19±0.09微摩尔(n = 19)。在有反应的保卫细胞中,外部施加ABA会使细胞质游离Ca2+浓度产生瞬时重复性增加。这些Ca2+瞬变伴随着同时出现的内向离子电流增加。膜去极化终止了细胞质Ca2+的重复性升高和内向离子电流,这表明ABA介导的Ca2+瞬变是由Ca2+从细胞外空间通过Ca2(+)渗透通道被动内流产生的。详细的电压钳测量表明,ABA激活的离子电流可以被超过 -10 mV的去极化所逆转。有趣的是,ABA诱导电流的逆转电位表明这些电流对Ca2+的选择性不高,从而允许Ca2+和K+都能通透。这些结果为ABA激活保卫细胞质膜上的Ca2(+)渗透离子通道提供了直接证据。ABA激活的离子通道允许细胞质Ca2+浓度重复性升高,进而可以调节促进气孔关闭的细胞反应。

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