Margiotta J F, Berg D K, Dionne V E
Department of Pharmacology, University of California, San Diego, La Jolla 92093.
J Neurosci. 1987 Nov;7(11):3612-22. doi: 10.1523/JNEUROSCI.07-11-03612.1987.
The properties of acetylcholine receptor (AChR) channels on chick ciliary ganglion neurons in culture were examined using patch-clamp recording techniques. Acetylcholine (ACh) was applied by rapid microperfusion. Whole-cell current noise analysis revealed a single class of functional receptors on the neurons. Dose-response studies indicated a Kd of about 36 microM and a Hill coefficient of 1.5-1.7, predicting 2 ACh binding sites per receptor. Both fast and slow components of receptor desensitization were observed. Single-channel recordings from excised outside-out patches of soma membrane exposed to 2-5 microM ACh indicated a single-channel conductance of 40 pS, a reversal potential of -9 mV, a mean open duration of 1 msec, and an opening probability of 0.34. The kinetic behavior of the channels was provisionally described by a 3-closed, 1-open state model for receptor activation. In all of these properties, AChRs of ciliary ganglion neurons resemble those on skeletal muscle fibers. Growing the neurons in an elevated K+ concentration produced a 2-3-fold decrease in peak whole-cell currents induced by ACh under standard test conditions, without altering any of the single-channel properties described above. Neither changes in cholinesterase activity nor receptor distribution accounted for the decrease. Instead, calculations indicated that elevated K+ reduced the ACh response by decreasing the number of functional AChRs on the neurons. No K+-dependent decrease is observed, however, in the number of total receptors on the neurons detected either by a monoclonal antibody specific for the receptor or by an alpha-neurotoxin that binds to the receptor and blocks its function. Moreover, the number of receptors detected by the 2 probes is at least 10-fold greater than the calculated number of functional receptors. The findings suggest that only a small fraction of the AChRs on the neuronal surface is functional and that the cell can alter the ratio of functional and nonfunctional receptors in response to growth conditions.
利用膜片钳记录技术,对培养的鸡睫状神经节神经元上乙酰胆碱受体(AChR)通道的特性进行了研究。通过快速微量灌注施加乙酰胆碱(ACh)。全细胞电流噪声分析揭示了神经元上存在单一类型的功能性受体。剂量反应研究表明,解离常数(Kd)约为36微摩尔,希尔系数为1.5 - 1.7,预测每个受体有2个ACh结合位点。观察到了受体脱敏的快速和慢速成分。对暴露于2 - 5微摩尔ACh的胞体膜外向膜片进行单通道记录,结果显示单通道电导为40皮西门子,反转电位为 - 9毫伏,平均开放持续时间为1毫秒,开放概率为0.34。通道的动力学行为初步用受体激活的三关闭、一开放状态模型进行描述。在所有这些特性方面,睫状神经节神经元的AChR与骨骼肌纤维上的AChR相似。在升高的钾离子浓度下培养神经元,在标准测试条件下,由ACh诱导的全细胞峰值电流降低了2 - 3倍,而上述任何单通道特性均未改变。胆碱酯酶活性的变化和受体分布均不能解释这种降低。相反,计算表明升高的钾离子通过减少神经元上功能性AChR的数量来降低ACh反应。然而,无论是用对该受体特异的单克隆抗体,还是用与该受体结合并阻断其功能的α - 神经毒素检测,均未观察到神经元上总受体数量有钾离子依赖性减少。此外,这两种探针检测到的受体数量至少比计算出的功能性受体数量大10倍。这些发现表明,神经元表面只有一小部分AChR具有功能,并且细胞能够根据生长条件改变功能性和非功能性受体的比例。