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Extracellular Ca2+ Ameliorates NaCl-Induced K+ Loss from Arabidopsis Root and Leaf Cells by Controlling Plasma Membrane K+-Permeable Channels1

机译:细胞外Ca2 +通过控制质膜K +-可渗透通道1缓解拟南芥根和叶细胞中NaCl诱导的K +损失1。

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摘要

Calcium can ameliorate Na+ toxicity in plants by decreasing Na+ influx through nonselective cation channels. Here, we show that elevated external [Ca2+] also inhibits Na+-induced K+ efflux through outwardly directed, K+-permeable channels. Noninvasive ion flux measuring and patch-clamp techniques were used to characterize K+ fluxes from Arabidopsis (Arabidopsis thaliana) root mature epidermis and leaf mesophyll under various Ca2+ to Na+ ratios. NaCl-induced K+ efflux was not related to the osmotic component of the salt stress, was inhibited by the K+ channel blocker TEA+, was not mediated by inwardly directed K+ channels (tested in the akt1 mutant), and resulted in a significant decrease in cytosolic K+ content. NaCl-induced K+ efflux was partially inhibited by 1 mm Ca2+ and fully prevented by 10 mm Ca2+. This ameliorative effect was at least partially attributed to a less dramatic NaCl-induced membrane depolarization under high Ca2+ conditions. Patch-clamp experiments (whole-cell mode) have demonstrated that two populations of Ca2+-sensitive K+ efflux channels exist in protoplasts isolated from the mature epidermis of Arabidopsis root and leaf mesophyll cells. The instantaneously activating K+ efflux channels showed weak voltage dependence and insensitivity to external and internal Na+. Another population of K+ efflux channels was slowly activating, steeply rectifying, and highly sensitive to Na+. K+ efflux channels in roots and leaves showed different Ca2+ and Na+ sensitivities, suggesting that these organs may employ different strategies to withstand salinity. Our results suggest an additional mechanism of Ca2+ action on salt toxicity in plants: the amelioration of K+ loss from the cell by regulating (both directly and indirectly) K+ efflux channels.
机译:钙可通过减少通过非选择性阳离子通道的Na +流入量来改善植物中的Na +毒性。在这里,我们显示升高的外部[Ca2 +]还通过向外定向的K +渗透通道抑制Na +诱导的K +外排。使用非侵入式离子通量测量和膜片钳技术来表征在各种Ca2 +与Na +比下来自拟南芥(Arabidopsis thaliana)根成熟表皮和叶肉叶的K +通量。 NaCl诱导的K +流出与盐胁迫的渗透成分无关,被K +通道阻滞剂TEA +抑制,不被内向型K +通道介导(在akt1突变体中进行了测试),并导致胞浆的显着减少K +内容。 NaCl诱导的K +外流被1 mm Ca2 +部分抑制,而被10 mm Ca2 +完全阻止。这种改善作用至少部分归因于在高Ca2 +条件下不太明显的NaCl诱导的膜去极化。膜片钳实验(全细胞模式)表明,从拟南芥根和叶肉细胞成熟的表皮中分离出的原生质体中存在两个Ca2 +敏感的K +外排通道。瞬时激活的K +外排通道显示出较弱的电压依赖性以及对外部和内部Na +的不敏感性。另一群K +外排通道正在缓慢激活,陡峭整流并对Na +高度敏感。根和叶中的K +外排通道显示出不同的Ca2 +和Na +敏感性,表明这些器官可能采用不同的策略来承受盐度。我们的结果表明,Ca2 +作用于植物的盐毒性的另一种机制是:通过调节(直接和间接地)K +外排通道来改善细胞中K +的损失。

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