Dravid Shashank M, Prakash Anand, Traynelis Stephen F
Department of Pharmacology, Emory University, Atlanta, GA 30322, USA.
J Physiol. 2008 Sep 15;586(18):4425-39. doi: 10.1113/jphysiol.2008.158634. Epub 2008 Jul 17.
The N-methyl-d-aspartate (NMDA) subtype of ionotropic glutamate receptors comprises both NR1 and NR2 subunits, and plays numerous roles in both physiological and pathophysiological processes in the central nervous system (CNS). NR2C-containing NMDA receptors are most abundant in cerebellum, thalamus and olfactory bulb, and are also expressed in oligodendrocytes and hippocampal interneurons. We have used patch clamp recording to explore the activation properties of recombinant NR1/NR2C receptors expressed in HEK293 cells. NR1/NR2C receptors activated by a maximally effective concentration of glutamate and glycine had two main conductance levels of 45 pS and 28 pS when the extracellular Ca(2+) concentration was 0.5 mm and the holding potential was -80 mV. The occurrence of the lower subconductance state was reduced in the absence of extracellular Ca(2+). The distribution of closed durations recorded from patches with a high probability of containing only one active channel were best fitted by five exponential functions; the apparent open duration histogram could be fitted by two exponential functions (n = 10 patches). The apparent mean open time of NR1/NR2C receptors was brief (0.52 +/- 0.04 ms), suggesting that the stability of the open state of the NR1/NR2C receptors is lower than other NR2-containing receptors. NR1/NR2C open probability was exceptionally low, being 0.011 +/- 0.002 in patches containing a single active receptor (n = 8). Fast agonist concentration jumps were performed on outside out patches with multiple NR1/NR2C channels, which activated with a 10-90% rise time of 3.9 +/- 0.4 ms, faster than other NR2-containing receptors. The deactivation time constant after a brief (5-8 ms) application of a maximally effective concentration of agonists was 319 +/- 34 ms. The majority of the patches also showed a modest level of desensitization that could be described by either a single or a double exponential time course with the fastest time constant between 15 and 47 ms. Conceptual models of activation were fitted using the maximum interval likelihood (MIL) method to the sequence of open and closed durations recorded from outside-out patches that contained one active NR1/NR2C channel. NR1/NR2C receptor properties including modest desensitization and low open probability could be described by gating schemes similar to those previously proposed for other NMDA receptor subunit combinations.
离子型谷氨酸受体的N-甲基-D-天冬氨酸(NMDA)亚型由NR1和NR2亚基组成,在中枢神经系统(CNS)的生理和病理生理过程中发挥着多种作用。含NR2C的NMDA受体在小脑、丘脑和嗅球中最为丰富,在少突胶质细胞和海马中间神经元中也有表达。我们利用膜片钳记录技术研究了在HEK293细胞中表达的重组NR1/NR2C受体的激活特性。当细胞外Ca(2+)浓度为0.5 mM且钳制电位为-80 mV时,由最大有效浓度的谷氨酸和甘氨酸激活的NR1/NR2C受体有两个主要电导水平,分别为45 pS和28 pS。在没有细胞外Ca(2+)的情况下,较低亚电导状态的出现减少。从很可能只包含一个活性通道的膜片记录的关闭持续时间分布最适合用五个指数函数拟合;表观开放持续时间直方图可以用两个指数函数拟合(n = 10个膜片)。NR1/NR2C受体的表观平均开放时间很短(0.52 +/- 0.04 ms),表明NR1/NR2C受体开放状态的稳定性低于其他含NR2的受体。NR1/NR2C的开放概率极低,在包含单个活性受体的膜片中为0.011 +/- 0.002(n = 8)。对具有多个NR1/NR2C通道的外侧向外膜片进行快速激动剂浓度阶跃,其激活的10-90%上升时间为3.9 +/- 0.4 ms,比其他含NR2的受体更快。在短暂(5-8 ms)施加最大有效浓度的激动剂后,失活时间常数为319 +/- 34 ms。大多数膜片还表现出适度的脱敏水平,可用单指数或双指数时间进程描述,最快时间常数在15至47 ms之间。使用最大间隔似然(MIL)方法将激活的概念模型拟合到从包含一个活性NR1/NR2C通道的外侧向外膜片记录的开放和关闭持续时间序列。NR1/NR2C受体的特性,包括适度的脱敏和低开放概率,可以用与先前为其他NMDA受体亚基组合提出的门控方案类似的方案来描述。