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鸡睫状神经节神经元上功能性乙酰胆碱受体的特性与调节

The properties and regulation of functional acetylcholine receptors on chick ciliary ganglion neurons.

作者信息

Margiotta J F, Berg D K, Dionne V E

机构信息

Department of Pharmacology, University of California, San Diego, La Jolla 92093.

出版信息

J Neurosci. 1987 Nov;7(11):3612-22. doi: 10.1523/JNEUROSCI.07-11-03612.1987.

Abstract

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.

摘要

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。

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