首页> 美国卫生研究院文献>The Journal of Physiology >Calcium-dependent inactivation of heteromeric NMDA receptor-channels expressed in human embryonic kidney cells.
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Calcium-dependent inactivation of heteromeric NMDA receptor-channels expressed in human embryonic kidney cells.

机译:钙依赖性失活的人类胚胎肾细胞中表达的异聚NMDA受体通道。

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摘要

1. Whole-cell current through heteromeric NR1-NR2A and NR1-NR2B subunit combinations of NMDA channels transiently expressed in human embryonic kidney cells (HEK 293) were studied using the patch-clamp technique. 2. With 4 mM Mg-ATP in the internal pipette solution, the responses of cells expressing NR1-NR2A channels to glutamate application gradually decreased, reaching 50% of control during the first 20 min of recording. This process was accompanied by acceleration of desensitization. 3. Conditioning (5-15 s) applications of glutamate (100 microM) induced a transient inactivation of NR1-NR2A and NR1-NR2B channels (20-40%) with a slow time course of recovery (tau r = 10-60 s). Both the degree of inactivation and the time constant of recovery increased with the duration of conditioning applications of glutamate, and with an elevation of Ca2+ in the external solution. 4. These results show that both NR1-NR2A and NR1-NR2B recombinant NMDA receptor-channels expressed in HEK 293 cells can be transiently inhibited by Ca2+ ions in a similar way to that described for hippocampal neurones.
机译:1.使用膜片钳技术研究了在人胚胎肾细胞(HEK 293)中瞬时表达的NMDA通道的异源NR1-NR2A和NR1-NR2B亚基组合的全细胞电流。 2.在内部移液器中使用4 mM Mg-ATP时,表达NR1-NR2A通道的细胞对谷氨酸施加的反应逐渐降低,在记录的前20分钟达到对照的50%。这个过程伴随着脱敏的加速。 3.谷氨酸(100 microM)的条件处理(5-15 s)引起NR1-NR2A和NR1-NR2B通道(20-40%)的瞬时失活,恢复过程缓慢(tau r = 10-60 s) )。灭活的程度和恢复的时间常数都随着调配谷氨酸的时间以及外部溶液中Ca2 +的升高而增加。 4.这些结果表明,HEK 293细胞中表达的NR1-NR2A和NR1-NR2B重组NMDA受体通道均可被Ca2 +离子以与海马神经元类似的方式瞬时抑制。

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