pH-dependent inhibition of voltage-gated H+ currents in rat alveolar epithelial cells by Zn2+ and other divalent cations

被引:147
作者
Cherny, VV [1 ]
DeCoursey, TE [1 ]
机构
[1] Rush Presbyterian St Lukes Med Ctr, Dept Mol Physiol & Biophys, Chicago, IL 60612 USA
关键词
metal binding constants; cadmium; pH; hydrogen ion; ion channels;
D O I
10.1085/jgp.114.6.819
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Inhibition by polyvalent cations is a defining characteristic of voltage-gated proton channels. The mechanism of this inhibition was studied in rat alveolar epithelial cells using tight-seal voltage clamp techniques. Metal concentrations were corrected for measured binding to buffers. Externally applied ZnCl2 reduced the H+ current, shifted die voltage-activation curve toward positive potentials, and slowed the turn-on of H+ current upon depolarization more than could be accounted for by a simple voltage shift, with minimal effects on the closing rate. The effects of Zn2+ were inconsistent with classical voltage-dependent block in which Zn2+ binds within the membrane voltage field. Instead, Zn2+ binds to superficial sites on the channel and modulates gating. The effects of extracellular Zn2+ were strongly pH(o) dependent but were insensitive to pH(i), suggesting that protons and Zn2+ compete for external sites on H+ channels. The apparent potency of Zn2+ in slowing activation was similar to 10X greater at pH(o) 7 than at pH(o) 6, and similar to 100X greater at pH(o) 6 than at pH(o) 5. The pH(o) dependence suggests that Zn2+, not ZnOH+, is the active species. Evidently, the Zn2+ receptor is formed by multiple groups, protonation of any of which inhibits Zn2+ binding. The external receptor bound H+ and Zn2+ with pk(a) 6.2-6.6 and pK(m) 6.5, as described by several models. Zn2+ effects on the proton chord conductance-voltage (g(H)-V) relationship indicated higher affinities, pk(a) 7 and pk(m) 8. CdCl2 had similar effects as ZnCl2 and competed with H+, but had lower affinity. Zn2+ applied internally via the pipette solution or to inside-out patches had comparatively small effects, but at high concentrations reduced H+ currents and slowed channel closing. Thus, external and internal zinc-binding sites are different. The external Zn2+ receptor may be the same modulatory protonation site(s) at which pH(o) regulates H+ channel gating.
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页码:819 / 838
页数:20
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