Amtmann A, Gradmann D
Pflanzenphysiologisches Institut der Universität, Göttingen, Germany.
J Membr Biol. 1994 Apr;139(2):117-25. doi: 10.1007/BF00232430.
Na(+)-selective microelectrodes with the sensor ETH 227 have been used to measure the cytoplasmic Na+ concentration, [Na+]c, in Acetabularia. In the steady-state, [Na+]c is about 60 mM (external 460 mM). Steps in external Na+ concentration, [Na+]o, cause biexponential relaxations of [Na+]c which have formally been described by a serial three-compartment model (outside<==>compartment 1<==>compartment 2). From the initial slopes (some mMsec-1) net uptake and release of about 3 mumolm-2sec-1 Na+ are determined. Surprisingly, but consistent with previous tracer flux measurements (Mummert, H., Gradmann, D. 1991. J. Membrane Biol, 124:255-263), these Na+ fluxes are not accompanied by corresponding changes of the transplasmalemma voltage. [Na+]c is neither affected by the membrane voltage, nor by electrochemical gradients of H+ or Cl- across the plasmalemma, nor by cytoplasmic ATP. The results suggest a powerful vesicular transport system for ions which bypasses the conductance of the plasmalemma. In addition, transient increases of [Na+]c have been observed to take place facultatively during action potentials. The exponential distribution of the amplitudes of these transients (many small and few large peaks) points to local events in the more ore less close vicinity of the Na+ recording electrode. These events are suggested to consist of disruption of endoplasmic vesicles due to a loss of pressure in the cytoplasm.
带有传感器ETH 227的钠选择性微电极已被用于测量伞藻细胞内的钠离子浓度[Na⁺]c。在稳态下,[Na⁺]c约为60 mM(胞外为460 mM)。胞外钠离子浓度[Na⁺]o的变化会导致[Na⁺]c呈双指数松弛,这一过程已用串联三室模型(外部⇔室1⇔室2)进行了形式上的描述。根据初始斜率(约为几mM·sec⁻¹)可确定钠离子的净摄取和释放速率约为3 μmol·m⁻²·sec⁻¹。令人惊讶的是,但与之前的示踪剂通量测量结果一致(Mummert, H., Gradmann, D. 1991. J. Membrane Biol, 124:255 - 263),这些钠离子通量并未伴随跨质膜电压的相应变化。[Na⁺]c既不受膜电压影响,也不受跨质膜的氢离子或氯离子电化学梯度影响,也不受细胞质ATP的影响。结果表明存在一个强大的离子囊泡运输系统,该系统绕过了质膜的电导。此外,在动作电位期间偶尔会观察到[Na⁺]c的短暂升高。这些瞬变幅度的指数分布(许多小峰和少数大峰)表明在钠离子记录电极或多或少的近距离内发生了局部事件。这些事件被认为是由于细胞质压力丧失导致内质囊泡破裂所致。