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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 117 (1990), S. 285-298 
    ISSN: 1432-1424
    Keywords: lens epithelium ; whole-cell recording ; cell culture ; K+ current ; Na+ current ; ion channel
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary The lens epithelial K+ conductance plays a key role in maintaining the lens ionic steady state. The specific channels responsible for this conductance are unknown. We used cultured lens epithelia and patch-clamp technology to address this problem. Human lens epithelial explants were cultured and after 1–4 passages were dissociated and used in this study. The cells from which we measured had a mean diameter of 31±1 μm (sem,n=26). The resting voltage was −19±4 mV (sem,n=10) and the input resistance was 2.5±0.5 GΩ (sem,n=17) at −60 mV. Two currents were prominent in whole-cell recordings. An outwardly rectifying current was seen in nearly every cell. The magnitude of this current was a function of K+ concentration and was blocked by 3mm tetraethylammonium. The instantaneous current-voltage relationship was linear in symmetric K+, implying that the outward rectificiation was due to gating. The current showed complex activation and inactivation kinetics. The second current seen was a transient inward current. This current had kinetics very similar to the traditional Na+ current of excitable cells and was blocked by 0.1 μm tetrodotoxin. In single-channel recordings, a 150-pS K+ channel and a 35-pS nonselective cation channel were seen but neither account for the macroscopic currents measured.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 114 (1990), S. 29-36 
    ISSN: 1432-1424
    Keywords: cornea ; endothelium ; potassium channel ; HCO 3 − ; Cl− ; anions ; patch clamp ; rabbit
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary The apical membrane of the rabbit corneal endothelium contains a potassium-selective ionic channel. In patch-clamp recordings, the probability of finding the channel in the open state (P o) depends on the presence of either HCO 3 − or Cl− in the bathing medium. In a methane sulfonate-containing bath,P o is 〈0.05 at all physiologically relevant transmembrane voltages. With 0mm [HCO 3 − ] o at +60 mV,P o was 0.085 and increased to 0.40 when [HCO 3 − ] o was 15mm. With 4mm [Cl−] o at +60 mV,P o was 0.083 and with 150mm Cl−,P o increased to 0.36. LowP o's are also found when propionate, sulphate, bromide, and nitrate are the primary bath anions. The mechanism of action of the anion-stimulated K+ channel gating is not yet known, but a direct action of pH seems unlikely. The alkalinization of cytoplasm associated with the addition of 10mm (NH4)2SO4 to the bath and the acidification accompanying its removal do not result in channel activation nor does the use of Nigericin to equilibrate intracellular pH with that of the bath over the pH range of 6.8 to 7.8. Channel gating also is not affected by bathing the internal surface of the patch with cAMP, cGMP, GTP-γ-s, Mg2+ or ATP. Blockers of Na/H+ exchange, Na+−HCO 3 − cotransport, Na+−K+ ATPase and carbonic anhydrase do not block the HCO 3 − stimulation ofP o. Several of the properties of the channel could explain some of the previously reported voltage changes that occur in corneal endothelial cells stimulated by extracellular anions.
    Type of Medium: Electronic Resource
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