Stephenson D T, Kushner P D
ALS and Neuromuscular Research Foundation, Pacific Presbyterian Medical Center, San Francisco, California 94115.
J Neurosci. 1988 Aug;8(8):3035-56. doi: 10.1523/JNEUROSCI.08-08-03035.1988.
The mature nervous system contains functional synaptic networks composed of neuronal sets and subsets whose identity and maintenance may rely on external surface molecules specific for these neuronal subdivisions. Such molecules may reside permanently on specific neurons, serving to identify those neurons within a complex population. From a collection of monoclonal antibodies made to the Torpedo cholinergic synaptosome preparation, we have identified several antibodies that bind the surface of some, but not all, neurons of the mature rat brain (Kushner and Stephenson, 1983; Kushner, 1984). In the present study we catalog which neurons of the entire rat brain and spinal cord are immunopositive for one of these antibodies, Tor 23. The atlas we have compiled can be used (1) on a practical level to guide affinity purifications and neuronal cell sorting, and (2) more esoterically to address whether surface antigenic sets of neurons share or define a common functional property. In the forebrain, Tor 23-positive neurons predominate as a rare cell type of the inner cortical laminae. In the midbrain, few cells stain. In the hindbrain, labeled neurons are dispersed among several nuclei. The exceptions to these observations, areas that almost exclusively contain Tor 23-immunopositive neurons, are the spinal cord ventral horn, the deep cerebellar nuclei, some cerebellar-related nuclei, selected auditory nuclei, the supraoptic and paraventricular nuclei of the hypothalamus, and the CA2 pyramidal neurons of the hippocampus. The neurons that bind Tor 23 are related biochemically by virtue of that shared epitope alone. Whether they are related in a functional manner is a separate issue. Tor 23 demarks many motor-related structures, specifically, the ventral horn motor lamina, the orofacial motor nuclei 5 and 7, the ambiguus nucleus, the deep cerebellar nuclei, the pontine reticulotegmental nucleus, the lateral reticular nucleus, the gigantocellular reticular nucleus, the red nucleus, and neurons within the motor and somatosensory cortices. The overlap of Tor 23 with motor structures suggests that Tor 23 is a motor system marker.
成熟的神经系统包含由神经元集和亚集组成的功能性突触网络,这些神经元集和亚集的特性及维持可能依赖于这些神经元亚群特有的细胞表面分子。此类分子可能永久存在于特定神经元上,用于在复杂的神经元群体中识别这些神经元。从针对电鳐胆碱能突触体制剂制备的一系列单克隆抗体中,我们鉴定出了几种能与成熟大鼠脑内部分而非全部神经元表面结合的抗体(库什纳和斯蒂芬森,1983年;库什纳,1984年)。在本研究中,我们梳理了整个大鼠脑和脊髓中哪些神经元对其中一种抗体Tor 23呈免疫阳性。我们编制的图谱可用于:(1)在实际层面指导亲和纯化和神经元细胞分选;(2)更深入地探讨神经元的表面抗原集是否共享或定义了一种共同的功能特性。在前脑,Tor 23阳性神经元作为内皮质板层中一种罕见的细胞类型占主导地位。在中脑,很少有细胞染色。在后脑,标记的神经元分散在几个核中。这些观察结果的例外情况,即几乎完全由Tor 23免疫阳性神经元组成的区域,是脊髓腹角、小脑深部核团、一些与小脑相关的核团、特定的听觉核团、下丘脑的视上核和室旁核以及海马体的CA2锥体神经元。仅凭借共享的表位,与Tor 23结合的神经元在生化上相关。它们在功能上是否相关则是另一个问题。Tor 23标记了许多与运动相关的结构,具体来说,包括腹角运动板层、口面部运动核团5和7、疑核、小脑深部核团、脑桥网状被盖核、外侧网状核、巨细胞网状核、红核以及运动和躯体感觉皮层内的神经元。Tor 23与运动结构的重叠表明Tor 23是一种运动系统标志物。