Lacaz-Vieira F
Department of Physiology and Biophysics, University of São Paulo, Brazil.
J Membr Biol. 1995 Nov;148(1):1-11. doi: 10.1007/BF00234151.
The present study focuses on two closely related topics on ion conductance in toad skins: (i) the interaction of apical protons with the apical voltage-dependent Cl(-)-activated channels of the mitochondria-rich cells, and (ii) the description and characterization of a novel subject, a voltage-dependent H(+)-activated conductance. The Cl- conductance (GCl) is activated by tissue hyperpolarization (which leads to apical membrane depolarization) and the presence of Cl- ions in the apical solution. Increasing apical proton concentration (from pH 8 to pH 4) impairs the process of activation of the Cl- conductive pathway, slowing the kinetics of It activation and reducing the steady-stage values of Gt and It. This effect is markedly voltage-dependent since no effect is seen at Vt = -100 mv and is fully present at -50 mV. The voltage-dependence of the pH effect suggests that the critical protonation sites of the apical Cl- channels are not freely exposed to the apical solution but dwell within the membrane electric field. An also coherent interpretation is that titration of apical proton binding sites affects the gating of the voltage-dependent Cl- channels, shifting the conductance-vs.-voltage curve to more negative clamping potentials. Tissue conductance in the absence of apical Cl- ions can be importantly affected by the pH of the apical solution (pHa), the effect being markedly dependent on the clamping potential. Generally speaking, the effect of rising apical proton concentration can be conspicuous at negative clamping potentials, while at positive potentials changes in tissue conductance were never observed. For a clamping potential of -100 mV, a turning point somewhere between pHa = 4 and pHa = 3 was observed. Apical acidification to pH 4 has no effect upon tissue conductance while apical acidification to pH 3 leads to a marked, slow and reversible increase of tissue conductance. A striking similitude exists between the voltage-dependent Cl(-)-gated conductance and the voltage-dependent proton-gated conductance regarding: (i) slow time courses of activation and deactivation, (ii) requirement for a negative clamping potential and the presence of a specific ion species in the apical solution for activation to take place, (iv) instantaneous ohmic behavior, and (v) steady-state rectification. However, so far the results do not permit one to conclude definitely that the voltage-dependent Cl(-)-gated conductance and the voltage-dependent proton-gated conductance share a common pathway.
(i)顶端质子与富含线粒体细胞的顶端电压依赖性Cl⁻激活通道的相互作用,以及(ii)一个新主题——电压依赖性H⁺激活电导的描述与特征。Cl⁻电导(GCl)由组织超极化(导致顶端膜去极化)以及顶端溶液中Cl⁻离子的存在所激活。增加顶端质子浓度(从pH 8到pH 4)会损害Cl⁻传导途径的激活过程,减缓其激活动力学并降低Gt和It的稳态值。这种效应显著依赖于电压,因为在Vt = -100 mV时未观察到效应,而在-50 mV时则完全显现。pH效应的电压依赖性表明,顶端Cl⁻通道的关键质子化位点并非自由暴露于顶端溶液中,而是处于膜电场内。另一种合理的解释是,顶端质子结合位点的滴定影响了电压依赖性Cl⁻通道的门控,使电导-电压曲线向更负的钳制电位移动。在没有顶端Cl⁻离子的情况下,组织电导会受到顶端溶液pH(pHa)的重要影响,这种效应显著依赖于钳制电位。一般来说,顶端质子浓度升高的效应在负钳制电位下可能很明显,而在正电位下从未观察到组织电导的变化。对于-100 mV的钳制电位,在pHa = 4和pHa = 3之间的某个位置观察到了一个转折点。顶端酸化至pH 4对组织电导没有影响,而顶端酸化至pH 3会导致组织电导显著、缓慢且可逆地增加。在电压依赖性Cl⁻门控电导和电压依赖性质子门控电导之间存在显著相似之处,具体体现在:(i)激活和失活的缓慢时间进程,(ii)对负钳制电位的要求以及顶端溶液中特定离子种类的存在以实现激活,(iv)瞬时欧姆行为,以及(v)稳态整流。然而,到目前为止,结果还不允许明确得出电压依赖性Cl⁻门控电导和电压依赖性质子门控电导共享共同途径的结论。