Buckley N J, Burnstock G
J Neurosci. 1986 Feb;6(2):531-40. doi: 10.1523/JNEUROSCI.06-02-00531.1986.
In order to localize the distribution of muscarinic receptors over the surface of cultured myenteric neurons, an autoradiographic procedure for detecting muscarinic receptors (using [3H]propylbenzilylcholine mustard; [3H]PrBCM) has been combined with an immunofluorescence procedure visualizing neuronal morphology (using an antibody raised against rat brain synaptosomes; anti-CTX). Using this technique, muscarinic receptors were localized over discrete areas of the neuronal cell surface. Receptors were seen to be widely distributed over the somata and neurites of 10-20% of cultured myenteric neurons. The greatest concentration of receptors occurred over the cell somata and proximal neurites. Receptors appeared evenly distributed over labeled cell somata, where their density was estimated to be between 30 and 100 receptors/micron2. Distal regions of neurites were labeled intermittently with some varicosities and intervaricosities being labeled while others were unlabeled. Growth cones and nerve endings of labeled neurites were consistently labeled. The ability to localize muscarinic receptors on a subpopulation of immunocytochemically identified neurons enhances our understanding of muscarinic neurotransmission in myenteric neurons and provides an experimental system for the investigation of regulatory influences on neuronal neurotransmitter receptor expression and distribution.
为了定位毒蕈碱受体在培养的肠肌间神经元表面的分布,一种检测毒蕈碱受体的放射自显影方法(使用[3H]丙基苄基胆碱氮芥;[3H]PrBCM)已与一种可视化神经元形态的免疫荧光方法(使用针对大鼠脑突触体产生的抗体;抗CTX)相结合。利用这种技术,毒蕈碱受体被定位在神经元细胞表面的离散区域。在10%-20%的培养肠肌间神经元的胞体和神经突上观察到受体分布广泛。受体的最大浓度出现在细胞胞体和近端神经突上。受体在标记的细胞胞体上分布均匀,据估计其密度在30至100个受体/微米2之间。神经突的远端区域被间歇性标记,一些膨体和膨体间区域被标记,而其他区域未被标记。标记神经突的生长锥和神经末梢始终被标记。在免疫细胞化学鉴定的神经元亚群上定位毒蕈碱受体的能力增强了我们对肠肌间神经元中毒蕈碱神经传递的理解,并为研究对神经元神经递质受体表达和分布的调节影响提供了一个实验系统。