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大鼠胃肠嗜铬样细胞中的电压门控性Ca2+电流

Voltage-gated Ca2+ currents in rat gastric enterochromaffin-like cells.

作者信息

Bufler J, Choi G C, Franke C, Schepp W, Prinz C

机构信息

Department of Neurology, Technical University of Munich, Germany.

出版信息

Am J Physiol. 1998 Feb;274(2):C424-9. doi: 10.1152/ajpcell.1998.274.2.C424.

Abstract

Enterochromaffin-like (ECL) cells are histamine-containing endocrine cells in the gastric mucosa that maintain a negative membrane potential of about -50 mV, largely due to voltage-gated K+ currents [D. F. Loo, G. Sachs, and C. Prinz. Am. J. Physiol. 270 (Gastrointest Liver Physiol. 33): G739-G745, 1996]. The current study investigated the presence of voltage-gated Ca2+ channels in single ECL cells. ECL cells were isolated from rat fundic mucosa by elutriation, density gradient centrifugation, and primary culture to a purity > 90%. Voltage-gated Ca2+ currents were measured in single ECL cells using the whole cell configuration of the patch-clamp technique. Depolarization-activated currents were recorded in the presence of Na+ or K+ blocking solutions and addition of 20 mM extracellular Ca2+. ECL cells showed inward currents in response to voltage steps that were activated at a test potential of around -20 mV with maximal inward currents observed at +20 mV and 20 mM extracellular Ca2+. The inactivation rate of the current decreased with increasingly negative holding potentials and was totally abolished at a holding potential of -30 mV. Addition of extracellular 20 mM Ba2+ instead of 20 mM Ca2+ increased the depolarization-induced current and decreased the inactivation rate. The inward current was fully inhibited by the specific L-type Ca2+ channel inhibitor verapamil (0.2 mM) and was augmented by the L-type Ca2+ channel activator BAY K 8644 (0.07 mM). We conclude that depolarization activates high-voltage-activated Ca2+ channels in ECL cells. Activation characteristics, Ba2+ effects, and pharmacological results imply the presence of L-type Ca2+ channels, whereas inactivation kinetics suggest the presence of additional N-type channels in rat gastric ECL cells.

摘要

肠嗜铬样(ECL)细胞是胃黏膜中含组胺的内分泌细胞,其维持约-50 mV的负膜电位,这主要归因于电压门控钾离子电流[D. F. 卢、G. 萨克斯和C. 普林兹。《美国生理学杂志》270卷(胃肠肝脏生理学33):G739 - G745,1996年]。当前研究调查了单个ECL细胞中电压门控钙通道的存在情况。通过淘洗、密度梯度离心和原代培养从大鼠胃底黏膜分离出ECL细胞,使其纯度>90%。使用膜片钳技术的全细胞配置在单个ECL细胞中测量电压门控钙电流。在存在钠或钾阻断溶液并添加20 mM细胞外钙的情况下记录去极化激活电流。ECL细胞在约-20 mV的测试电位时对电压阶跃产生内向电流,在+20 mV和20 mM细胞外钙时观察到最大内向电流。电流的失活速率随着保持电位越来越负而降低,在-30 mV的保持电位时完全消除。添加细胞外20 mM钡离子而非20 mM钙离子可增加去极化诱导的电流并降低失活速率。内向电流被特异性L型钙通道抑制剂维拉帕米(0.2 mM)完全抑制,并被L型钙通道激活剂BAY K 8644(0.07 mM)增强。我们得出结论,去极化激活ECL细胞中的高电压激活钙通道。激活特性、钡离子效应和药理学结果表明存在L型钙通道,而失活动力学表明大鼠胃ECL细胞中存在额外的N型通道。

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