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首页> 外文期刊>Protoplasma: An International Journal of Cell Biology >Stringent control of cytoplasmic Ca2+ in guard cells of intact plants compared to their counterparts in epidermal strips or guard cell protoplasts
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Stringent control of cytoplasmic Ca2+ in guard cells of intact plants compared to their counterparts in epidermal strips or guard cell protoplasts

机译:与表皮条或保卫细胞原生质体中相应植物相比,完整植物保卫细胞中细胞质Ca2 +的严格控制

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Cytoplasmic calcium elevations, transients, and oscillations are thought to encode information that triggers a variety of physiological responses in plant cells. Yet Ca2+ signals induced by a single stimulus vary, depending on the physiological state of the cell and experimental conditions. We compared Ca2+ homeostasis and stimulus-induced Ca2+ signals in guard cells of intact plants, epidermal strips, and isolated protoplasts. Single-cell ratiometric imaging with the Ca2+-sensitive dye Fura 2 was applied in combination with electrophysiological recordings. Guard cell protoplasts were loaded with Fura 2 via a patch pipette, revealing a cytoplasmic free Ca2+ concentration of around 80 nM at -47 mV. Upon hyperpolarization of the plasma membrane to -107 mV, the Ca2+ concentration increased to levels exceeding 400 nM. Intact guard cells were able to maintain much lower cytoplasmic free Ca2+ concentrations at hyperpolarized potentials, the average concentration at -100 mV was 183 and 90 nM in epidermal strips and intact plants, respectively. Further hyperpolarization of the plasma membrane to -160 mV induced a sustained rise of the guard cell cytoplasmic Ca2+ concentration, which slowly returned to the prestimulus level in intact plants but not in epidermal strips. Our results show that cytoplasmic Ca2+ concentrations are stringently controlled in guard cells of intact plants but become increasingly more sensitive to changes in the plasma membrane potential in epidermal strips and isolated protoplasts.
机译:细胞质钙的升高,瞬变和振荡被认为编码了触发植物细胞中各种生理反应的信息。然而,由单个刺激诱导的Ca2 +信号会根据细胞的生理状态和实验条件而变化。我们在完整植物,表皮条和分离的原生质体的保卫细胞中比较了Ca2 +稳态和刺激诱导的Ca2 +信号。结合使用Ca2 +敏感染料Fura 2的单细胞比例成像与电生理记录相结合。通过贴片移液器将Fura 2加载到保卫细胞原生质体中,显示在-47 mV时约80 nM的细胞质游离Ca2 +浓度。当质膜超极化至-107 mV时,Ca2 +浓度增加至超过400 nM的水平。完整的保卫细胞能够在超极化电势下维持低得多的胞质游离Ca2 +浓度,在表皮条和完整植物中,-100 mV的平均浓度分别为183和90 nM。质膜进一步超极化至-160 mV导致保卫细胞胞质Ca2 +浓度持续升高,在完整植株中缓慢返回到刺激前水平,但在表皮条中则没有。我们的结果表明,完整植物的保卫细胞中细胞质Ca2 +的浓度受到严格控制,但对表皮条和分离的原生质体中质膜电位的变化变得越来越敏感。

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