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豚鼠膀胱肌细胞中牵张激活通道的特性

Properties of stretch-activated channels in myocytes from the guinea-pig urinary bladder.

作者信息

Wellner M C, Isenberg G

机构信息

Department of Physiology, University of Cologne, Germany.

出版信息

J Physiol. 1993 Jul;466:213-27.

PMID:7692040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1175475/
Abstract
  1. Stretch-activated channels (SACs) were analysed on patches attached to myocytes isolated from the guinea-pig urinary bladder. At 22 degrees C application of -2 to -4 kPa to the patch electrode induced SACs at a density of one to two per patch (3-5 M omega electrodes). 2. With electrodes containing 145 mM K+, 20 mM TEA and 2 mM Mg2+, the single channel current followed a linear I-V curve with a slope conductance of 39 +/- 5 pS (mean +/- S.D.) and a reversal potential of 2 +/- 6 mV. Substitution of chloride by aspartate ions left both parameters unchanged suggesting that the anions do not contribute to the currents. 3. Hyperpolarization from -30 to -80 mV did not open channels by itself but increased channel activity (NPo; where N is the number of channels in the patch and Po is the probability of the channel being open) twofold. The hyperpolarization-induced increase in NPo can be attributed to a reduction of long closures. At positive patch potentials numerous blank records strongly diminished NPo. 4. Inward currents through SACs can be carried by a variety of cations. In the presence of 2 mM Mg2+, the respective channel conductance was 40 +/- 4 pS for 140 mM K+ > 34 +/- 2 pS for 140 mM Na+ > or = 33 +/- 6 pS for 140 mM Cs+ > 19 +/- 2 pS for 110 mM Ba2+ > 17 +/- 2 pS for 110 mM Ca2+. 5. Reduction of CaCl2 from 110 to 10 mM did not change the conductance but shifted the reversal potential from +7 to -7 mV; the reversal potentials suggest that SACs are slightly more permeable for Ca2+ than for K+. 6. In the absence of divalent cations, the conductance of K+ was 82 +/- 4 pS for inward but 45 pS for outward currents. Addition of either 2 mM Ca2+ or 2 mM Mg2+ reduced the conductance for inward currents to 40 pS. 7. The change from 140 to 14 mM KCl plus 136 mM Tris-Cl reduced the conductance from 82 to 56 pS whereas the reversal potential shifted only from -4 to -9 mV. When 20 mM K+ and 300 mM sucrose were applied, the conductance fell to 39 pS and the reversal potential shifted by -30 mV. The results suggest that Tris+ can permeate through SACs when extracellular divalent cations are absent.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 在与从豚鼠膀胱分离的心肌细胞相连的膜片上分析牵张激活通道(SACs)。在22℃时,向膜片电极施加-2至-4kPa的压力可诱导SACs,每个膜片的密度为1至2个(3-5MΩ电极)。2. 使用含有145mM K⁺、20mM四乙铵(TEA)和2mM Mg²⁺的电极时,单通道电流遵循线性I-V曲线,斜率电导为39±5pS(平均值±标准差),反转电位为2±6mV。用天冬氨酸离子替代氯离子后,这两个参数均未改变,表明阴离子对电流无贡献。3. 从-30mV超极化至-80mV本身不会打开通道,但会使通道活性(NPo;其中N是膜片中通道的数量,Po是通道开放的概率)增加两倍。超极化诱导的NPo增加可归因于长关闭时间的减少。在正的膜片电位下,大量空白记录显著降低了NPo。4. 通过SACs的内向电流可由多种阳离子携带。在存在2mM Mg²⁺的情况下,对于140mM K⁺,相应的通道电导为40±4pS;对于140mM Na⁺,为34±2pS;对于140mM Cs⁺,≥33±6pS;对于110mM Ba²⁺,为19±2pS;对于110mM Ca²⁺,为17±2pS。5. 将CaCl₂从110mM降至10mM不会改变电导,但会使反转电位从+7mV变为-7mV;反转电位表明SACs对Ca²⁺的通透性略高于对K⁺的通透性。6. 在不存在二价阳离子的情况下,K⁺的内向电导为82±4pS,外向电导为45pS。添加2mM Ca²⁺或2mM Mg²⁺均可将内向电流的电导降低至40pS。7. 将140mM KCl变为14mM KCl加136mM Tris-Cl会使电导从82pS降至56pS,而反转电位仅从-4mV变为-9mV。当施加20mM K⁺和300mM蔗糖时,电导降至39pS,反转电位偏移-30mV。结果表明,当细胞外不存在二价阳离子时,Tris⁺可透过SACs。(摘要截断于400字)

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