Sieve Element Ca2+ Channels as Relay Stations between Remote Stimuli and Sieve Tube Occlusion in Vicia faba
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Sieve Element Ca2+ Channels as Relay Stations between Remote Stimuli and Sieve Tube Occlusion in Vicia faba

机译:蚕豆蚕丝中Ca2 +通道作为远程刺激和筛管阻塞之间的中继站

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nnnDamage induces remote occlusion of sieve tubes in Vicia faba by forisome dispersion, triggered during the passage of an electropotential wave (EPW). This study addresses the role of Ca2+ channels and cytosolic Ca2+ elevation as a link between EPWs and forisome dispersion. Ca2+ channel antagonists affect the initial phase of the EPW as well as the prolonged plateau phase. Resting levels of sieve tube Ca2+ of ~50 nM were independently estimated using Ca2+-selective electrodes and a Ca2+-sensitive dye. Transient changes in cytosolic Ca2+ were observed in phloem tissue in response to remote stimuli and showed profiles similar to those of EPWs. The measured elevation of Ca2+ in sieve tubes was below the threshold necessary for forisome dispersion. Therefore, forisomes need to be associated with Ca2+ release sites. We found an association between forisomes and endoplasmic reticulum (ER) at sieve plates and pore-plasmodesma units where high-affinity binding of a fluorescent Ca2+ channel blocker mapped an increased density of Ca2+ channels. In conclusion, propagation of EPWs in response to remote stimuli is linked to forisome dispersion through transiently high levels of parietal Ca2+, release of which depends on both plasma membrane and ER Ca2+ channels.
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nnnDamage导致蚕豆 中的筛管远程阻塞由电势 波(EPW)通过时触发的分散。这项研究探讨了Ca 2 + 通道和 胞质Ca 2 + 升高作为EPW与主要 分散。 Ca 2 + 通道拮抗剂会影响EPW的初始阶段 以及延长的高原期。 “〜” 50 nM的筛管Ca 2 + 的静置水平 独立使用 Ca 2 + 选择电极和Ca 2 + 敏感染料进行估算。在韧皮部组织中, 对远程刺激的反应中,细胞质中Ca 2 + 的瞬时 发生了变化,并且与 EPW。在筛管中测得的Ca 2 + 的高度低于 分散所需的阈值。因此, 异构体需要与Ca 2 + 释放位点相关。我们 在筛板和孔-等离子胞浆单元处发现了形态和内质网 (ER)之间的关联,其中荧光Ca的高亲和力 结合 2 + 通道阻滞剂映射了Ca 2 + 通道增加的 密度。综上所述,EPWs 的繁殖是通过瞬时高水平的顶叶Ca 2 + ,释放< SUP> 取决于质膜和ER Ca 2 + 通道。

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  • 来源
    《THE PLANT CELL》 |2009年第7期|2118-2132|共15页
  • 作者单位

    Plant Cell Biology Research Group, Institute of General Botany, Justus-Liebig-University, D-35390 Giessen, Germany;

    Plant Cell Biology Research Group, Institute of General Botany, Justus-Liebig-University, D-35390 Giessen, Germany;

    Department of Plant Sciences, University of Oxford, Oxford, OX1 3RB, United Kingdom;

    Institute of General Botany, Justus-Liebig-University, D-35390 Giessen, Germany;

    Plant Cell Biology Research Group, Institute of General Botany, Justus-Liebig-University, D-35390 Giessen, Germany;

    Plant Cell Biology Research Group, Institute of General Botany, Justus-Liebig-University, D-35390 Giessen, Germany;

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