Suzue T, Kaprielian Z, Patterson P H
Division of Biology, California Institute of Technology, Pasadena 91125.
Neuron. 1990 Oct;5(4):421-31. doi: 10.1016/0896-6273(90)90081-p.
Spinal cord axons display a rostrocaudal, positional bias in their innervation of sympathetic ganglia and intercostal skeletal muscles. In an effort to examine the molecular basis of this positional specificity, we used the cyclophosphamide immunosuppression method to produce monoclonal antibodies that bind preferentially to rostral ganglia. The staining distribution of one of these antibodies, ROCA1, has been analyzed using a novel histological method. A graded decline in binding is observed along the chain of adult rat sympathetic ganglia, as well as in the nerves innervating intercostal muscles. The antigen is identified on immunoblots as a 65 kd protein, whose distribution corresponds to the pattern found histologically. Surprisingly, ROCA1 appears to bind to glial cells, implying rostrocaudal, molecular differences in their surfaces.
脊髓轴突在其对交感神经节和肋间骨骼肌的神经支配中表现出一种从尾到头的位置偏向性。为了研究这种位置特异性的分子基础,我们使用环磷酰胺免疫抑制方法制备了优先结合头端神经节的单克隆抗体。其中一种抗体ROCA1的染色分布已通过一种新的组织学方法进行了分析。在成年大鼠交感神经节链以及支配肋间肌的神经中,观察到结合力呈梯度下降。在免疫印迹上,该抗原被鉴定为一种65千道尔顿的蛋白质,其分布与组织学上发现的模式相对应。令人惊讶的是,ROCA1似乎与神经胶质细胞结合,这意味着它们表面存在从尾到头的分子差异。