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功能不同的αβγεGABA(A)受体形成的证据。

Evidence for the formation of functionally distinct alphabetagammaepsilon GABA(A) receptors.

作者信息

Davies P A, Kirkness E F, Hales T G

机构信息

Department of Pharmacology, The George Washington University Medical Center, 2300 Eye Street NW, Washington DC 20037, USA.

出版信息

J Physiol. 2001 Nov 15;537(Pt 1):101-13. doi: 10.1111/j.1469-7793.2001.0101k.x.

DOI:10.1111/j.1469-7793.2001.0101k.x
PMID:11711565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2278943/
Abstract
  1. We transiently introduced the human GABA(A) receptor epsilon subunit cDNA into a human embryonic kidney (HEK) cell line stably expressing alpha1beta3gamma2 receptors (WSS-1 cells) to establish whether the subunit competes with the gamma2 subunit for assembly into receptors. GABA-evoked currents were recorded using the patch-clamp technique from cells transfected with cDNA encoding green fluorescent protein (GFP) alone or in combination with the epsilon subunit cDNA. 2. The epsilon subunit did not change the potency of GABA: the GABA EC(50) was 34 +/- 6 microM in control WSS-1 cells and 37 +/- 6 microM in cells expressing the epsilon subunit. The introduction of the epsilon subunit reduced the peak current amplitude activated by GABA (1 mM) from 1.8 +/- 0.2 nA in control cells to 0.9 +/- 0.2 nA in cells expressing the epsilon subunit (P < 0.05). 3. The epsilon subunit caused the appearance of leak currents recorded in the absence of GABA. Outside-out patches excised from epsilon subunit-containing WSS-1 cells exhibited spontaneously opening GABA(A) channels not seen in patches excised from control GFP-expressing WSS-1 cells. Introduction of the epsilon subunit did not alter the GABA-evoked single-channel cord conductance. 4. The anaesthetic 2,6-diisopropylphenol (propofol, 3 microM) and the benzodiazepine flunitrazepam (1 microM) potentiated GABA-evoked currents recorded from control cells labelled with GFP. The epsilon subunit reduced potentiation by both agents 48-96 h after transfection. 5. The introduction of the epsilon subunit had no effect on the ability of propofol (3-30 microM) relative to GABA (1 mM) to activate GABA(A) receptors in WSS-1 cells. High concentrations of propofol (> or = 100 microM) produced a more marked desensitization of GABA(A) receptor activity in WSS-1 cells transfected with cDNA for the epsilon subunit than in control cells. 6. There was no difference in the potency of Zn(2+) as an inhibitor of currents recorded from control cells (IC(50) = 165 +/- 34 microM) or cells expressing the epsilon subunit (IC(50) = 179 +/- 11 microM). 7. GABA-activated currents recorded both from control cells and cells expressing the epsilon subunit reversed in sign at the Cl- equilibrium potential and exhibited outward rectification. 8. The introduction of the epsilon subunit changes the functional properties of GABA(A) receptors in WSS-1 cells. The resulting receptors have a unique combination of properties indicative of the co-assembly of alpha, beta, gamma and epsilon subunits.
摘要
  1. 我们将人γ-氨基丁酸A(GABA(A))受体ε亚基的互补DNA(cDNA)瞬时导入稳定表达α1β3γ2受体的人胚肾(HEK)细胞系(WSS-1细胞),以确定该亚基是否与γ2亚基竞争组装成受体。使用膜片钳技术记录单独转染编码绿色荧光蛋白(GFP)的cDNA或同时转染ε亚基cDNA的细胞中GABA诱发的电流。2. ε亚基不改变GABA的效价:在对照WSS-1细胞中GABA的半数有效浓度(EC(50))为34±6微摩尔,在表达ε亚基的细胞中为37±6微摩尔。ε亚基的导入使GABA(1毫摩尔)激活的峰值电流幅度从对照细胞中的1.8±0.2纳安降低到表达ε亚基细胞中的0.9±0.2纳安(P<0.05)。3. ε亚基导致在无GABA时记录到泄漏电流。从含ε亚基的WSS-1细胞上切下的外向型膜片显示出自发性开放的GABA(A)通道,而在从表达对照GFP的WSS-1细胞上切下的膜片中未见到。ε亚基的导入未改变GABA诱发的单通道弦电导。4. 麻醉剂2,6-二异丙基苯酚(丙泊酚,3微摩尔)和苯二氮䓬类药物氟硝西泮(1微摩尔)增强了从用GFP标记的对照细胞中记录到的GABA诱发的电流。转染后48 - 96小时,ε亚基降低了两种药物的增强作用。5. ε亚基的导入对丙泊酚(3 - 30微摩尔)相对于GABA(1毫摩尔)激活WSS-1细胞中GABA(A)受体的能力没有影响。高浓度丙泊酚(≥100微摩尔)在转染了ε亚基cDNA的WSS-1细胞中比在对照细胞中对GABA(A)受体活性产生更明显的脱敏作用。6. 锌离子(Zn(2+))作为对照细胞(半数抑制浓度(IC(50))= 165±34微摩尔)或表达ε亚基细胞(IC(50) = 179±11微摩尔)中电流抑制剂的效价没有差异。7. 从对照细胞和表达ε亚基的细胞中记录到的GABA激活电流在氯离子平衡电位处反转符号,并表现出外向整流。8. ε亚基的导入改变了WSS-1细胞中GABA(A)受体的功能特性。产生的受体具有独特的特性组合,表明α、β、γ和ε亚基共同组装。

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