Departments of Paediatrics, Pathology (Neuropathology) and Clinical Neurosciences (Neurology and Neurosurgery), University of Calgary Faculty of Medicine and Alberta Children's Hospital Research Institute, Calgary, Alta., Canada.
Dev Neurosci. 2013;35(4):317-25. doi: 10.1159/000351031. Epub 2013 Jun 20.
Precise temporal and spatial sequences of synaptogenesis were demonstrated in 172 human foetuses and neonates post-mortem in transverse paraffin sections of pons and cerebellar vermis and hemispheres, using synaptophysin immunoreactivity of this protein of synaptic vesicular walls. The pontine nuclei exhibit a transitory patchy pattern not predicted from the uniform histology and reminiscent of the corpus striatum; synaptic vesicle reactivity appears at 20 weeks and is uniform by 34 weeks. In the cerebellar cortex, the vermis matures sooner than the cerebellar hemispheres and the paravermal portions earlier than the lateral folia. The earliest synapses occur around the somata of Purkinje neurons and later in the internal granular layer, but synaptic glomeruli are not well formed until after 26 weeks. The normal patterns here shown, together with earlier data of the Guillain-Mollaret triangle, provide controls for the interpretation of synaptic delay or precociousness and other pathological patterns in malformations, genetic/metabolic conditions and prenatal acquired insults affecting the human foetus.
使用突触小泡膜上这种蛋白质的突触小泡蛋白免疫反应,在死后横切石蜡切片的脑桥和小脑蚓部和半球中,对 172 个人胎和新生儿进行了研究,展示了突触发生的精确时间和空间顺序。脑桥核呈现出一种非均匀组织学所不能预测的、短暂的斑片状模式,使人联想到纹状体;突触小泡反应性在 20 周时出现,到 34 周时变得均匀。在小脑皮质中,蚓部比半球成熟得更早,蚓旁部比外侧叶更早。最早的突触发生在浦肯野神经元的胞体周围,然后在内颗粒层中出现,但突触小球直到 26 周后才形成良好。这里显示的正常模式,以及更早的 Guillain-Mollaret 三角的数据,为解释突触延迟或早熟以及其他影响人类胎儿的畸形、遗传/代谢状况和产前获得性损伤的病理性模式提供了对照。