DiFiglia M, Roberts R C, Benowitz L I
Laboratory of Cellular Neurobiology, Massachusetts General Hospital, Boston 02129.
J Comp Neurol. 1990 Dec 22;302(4):992-1001. doi: 10.1002/cne.903020421.
GAP-43 is a neuron-specific phosphoprotein that has been implicated in neuronal development, axonal regeneration, and synaptic plasticity. Although in mammals the caudate-putamen is among those brain areas that retain a high content of GAP-43 throughout life, the role of the phosphoprotein in the neostriatum is unknown. In order to understand better the possible function(s) of GAP-43 in the adult striatum, its cellular localization was examined with immunohistochemistry at the light and electron microscopic levels by using a sheep polyclonal antibody. At the light microscopic level immunoreactive GAP-43 was abundant throughout the neostriatal neuropil but was absent from neuronal somata. At the ultrastructural level, labeling was most prevalent in small unmyelinated axons (0.12-0.15 microns diameter). Reaction product was distributed along fibers in discrete patches about 1 micron apart and in preterminal sites from which vesicle-filled boutons arose. Staining was also present in small (0.35 microns) axon terminals that contained round vesicles and formed asymmetric synapses, mostly with thin spines. Following unilateral cortical lesions, some degenerating cortical axons in the neostriatum exhibited GAP-43 labeling. Unexpectedly, in normal striatum, GAP-43 was also occasionally found in the heads of dendritic protrusions and in thin spines that received asymmetric contacts. We speculate that in the adult neostriatum, the protein may be important in the remodeling of synapses onto medium spiny neurons that involve, in part, the corticostriatal pathway.
生长相关蛋白43(GAP - 43)是一种神经元特异性磷蛋白,与神经元发育、轴突再生和突触可塑性有关。尽管在哺乳动物中,尾状核 - 壳核是终生保留高含量GAP - 43的脑区之一,但该磷蛋白在新纹状体中的作用尚不清楚。为了更好地理解GAP - 43在成年纹状体中可能的功能,我们使用绵羊多克隆抗体,通过免疫组织化学在光镜和电镜水平上检测了其细胞定位。在光镜水平,免疫反应性GAP - 43在整个新纹状体神经毡中丰富,但在神经元胞体中不存在。在超微结构水平,标记最常见于小的无髓轴突(直径0.12 - 0.15微米)。反应产物沿着纤维分布在相距约1微米的离散斑块中以及囊泡填充的终扣出现的终末前位点。染色也存在于小的(0.35微米)轴突终末,这些终末含有圆形囊泡并形成不对称突触,主要与细棘突形成突触。单侧皮质损伤后,新纹状体中一些退化的皮质轴突显示出GAP - 43标记。出乎意料的是,在正常纹状体中,偶尔也能在树突突起的头部和接受不对称接触的细棘突中发现GAP - 43。我们推测,在成年新纹状体中,该蛋白可能在涉及部分皮质 - 纹状体通路的中等棘状神经元突触重塑中起重要作用。