首页> 美国卫生研究院文献>The Plant Cell >Calcium-Activated K+ Channels and Calcium-Induced Calcium Release by Slow Vacuolar Ion Channels in Guard Cell Vacuoles Implicated in the Control of Stomatal Closure.
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Calcium-Activated K+ Channels and Calcium-Induced Calcium Release by Slow Vacuolar Ion Channels in Guard Cell Vacuoles Implicated in the Control of Stomatal Closure.

机译:保卫细胞液泡中钙激活的K +通道和钙离子通过缓慢的液泡离子通道释放的钙诱导的钙释放参与了气孔闭合的控制。

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摘要

Stomatal closing requires the efflux of K+ from the large vacuolar organelle into the cytosol and across the plasma membrane of guard cells. More than 90% of the K+ released from guard cells during stomatal closure originates from the guard cell vacuole. However, the corresponding molecular mechanisms for the release of K+ from guard cell vacuoles have remained unknown. Rises in the cytoplasmic Ca2+ concentration have been shown to trigger ion efflux from guard cells, resulting in stomatal closure. Here, we report a novel type of largely voltage-independent K+-selective ion channel in the vacuolar membrane of guard cells that is activated by physiological increases in the cytoplasmic Ca2+ concentration. These vacuolar K+ (VK) channels had a single channel conductance of 70 pS with 100 mM KCI on both sides of the membrane and were highly selective for K+ over NH4+ and Rb+. Na+, Li+, and Cs+ were not measurably permeant. The Ca2+, voltage, and pH dependences, high selectivity for K+, and high density of VK channels in the vacuolar membrane of guard cells suggest a central role for these K+ channels in the initiation and control of K+ release from the vacuole to the cytoplasm required for stomatal closure. The activation of K+-selective VK channels can shift the vacuolar membrane to more positive potentials on the cytoplasmic side, sufficient to activate previously described slow vacuolar cation channels (SV-type). Analysis of the ionic selectivity of SV channels demonstrated a Ca2+ over K+ selectivity (permeability ratio for Ca2+ to K+ of ~3:1) of these channels in broad bean guard cells and red beet vacuoles, suggesting that SV channels play an important role in Ca2+-induced Ca2+ release from the vacuole during stomatal closure. A model is presented suggesting that the interaction of VK and SV channel activities is crucial in regulating vacuolar K+ and Ca2+ release during stomatal closure. Furthermore, the possibility that the ubiquitous SV channels may represent a general mechanism for Ca2+-induced Ca2+ release from higher plant vacuoles is discussed.
机译:气孔关闭需要钾离子从大的液泡细胞器流出到细胞质中,并穿过保卫细胞的质膜。气孔关闭期间从保卫细胞释放的K +的90%以上来自保卫细胞液泡。然而,从保卫细胞液泡释放K +的相应分子机制仍然未知。业已证明,细胞质Ca2 +浓度升高会触发保卫细胞的离子流出,从而导致气孔关闭。在这里,我们报告了新型的类型的保卫细胞的液泡膜中的很大程度上不依赖电压的K +选择性离子通道,该通道被细胞质Ca2 +浓度的生理增加所激活。这些液泡的K +(VK)通道在膜的两侧均具有100 mM KCI的单通道电导为70 pS,并且对NH4 +和Rb +的K +具有高度选择性。 Na +,Li +和Cs +的渗透性不明显。 Ca2 +,电压和pH依赖性,对K +的高选择性以及保卫细胞液泡膜中VK通道的高密度表明,这些K +通道在引发和控制K +从液泡向所需细胞质的释放中起着核心作用。用于气孔闭合。 K +选择性VK通道的激活可以将液泡膜转移到细胞质侧更多的正电位,足以激活先前描述的缓慢液泡阳离子通道(SV型)。对SV通道离子选择性的分析表明,在蚕豆保卫细胞和红甜菜液泡中这些通道的Ca2 +相对于K +选择性(Ca2 +与K +的渗透比为〜3:1),表明SV通道在Ca2 +中起重要作用气孔关闭期间,诱导的Ca2 +从液泡释放。提出了一个模型,表明在气孔关闭过程中,VK和SV通道活性的相互作用对于调节液泡K +和Ca2 +的释放至关重要。此外,讨论了普遍存在的SV通道可能代表从较高的植物液泡释放Ca2 +诱导的Ca2 +的一般机制的可能性。

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