Selçuki M, Manning S, Bernfield M
Department of Neurosurgery, University of Celal Bayar, School of Medicine, Manisa, Turkey.
Childs Nerv Syst. 2001 Jan;17(1-2):19-23. doi: 10.1007/s003810000401.
The paralysis associated with lumbosacral meningomyelocele has been attributed both to myelodysplasia and to degeneration of the exposed neural tissue. Surgically created dysraphism shows that exposure of an intact spinal cord in a genetically normal animal results in degeneration of the normal nervous tissue and subsequent paralysis. Our objective was to study neuronal differentiation in the curly tail mouse mutant model, which develops lumbosacral meningomyelocele naturally and is a phenocopy of nonsyndromic human neural tube defects. Prenatal repair of meningomyelocele assumes that the normal neuronal differentiation program occurs despite failure of neurulation. Here we demonstrate that this most suitable animal model has normal differentiation of neuronal structures at the level of the meningomyelocele. TuJ1, an antibody to neuronal specific class III beta-tubulin, an early marker of neuronal differentiation, was used to stain paraffin-embedded sections of curly tail mouse embryo meningomyelocele. Embryos were examined at embryonic day 13.5 (E13.5). The inbred mouse strain, C57BL6/J, which is genetically similar to the curly tail mouse, was used as a control in these studies. We show that early neuronal differentiation appears intact within the meningomyelocele. TuJ stains structures within the open neural tube. Motor neurons are present in the ventral horn and ventral roots. Dorsal root ganglia are present and of similar size to controls. The staining pattern is similar to that seen in the C57BL/6J control mouse, although dorsal structures are laterally displaced in the curly tail meningomyelocele. Based on this model, fetal surgery to repair human meningomyelocele may preserve neurological function in those cases where there is not an inherent genetic defect of the neural tissue.
与腰骶部脊髓脊膜膨出相关的瘫痪一直被归因于脊髓发育异常和暴露的神经组织变性。手术造成的脊柱裂显示,在基因正常的动物中暴露完整的脊髓会导致正常神经组织变性及随后的瘫痪。我们的目的是研究卷尾小鼠突变模型中的神经元分化,该模型自然发生腰骶部脊髓脊膜膨出,是人类非综合征性神经管缺陷的拟表型。脊髓脊膜膨出的产前修复假定,尽管神经形成失败,但正常的神经元分化程序仍会发生。在此,我们证明这个最合适的动物模型在脊髓脊膜膨出水平具有正常的神经元结构分化。TuJ1是一种针对神经元特异性III类β微管蛋白的抗体,它是神经元分化的早期标志物,用于对卷尾小鼠胚胎脊髓脊膜膨出的石蜡包埋切片进行染色。在胚胎第13.5天(E13.5)对胚胎进行检查。近交系小鼠品系C57BL6/J与卷尾小鼠基因相似,在这些研究中用作对照。我们表明,脊髓脊膜膨出内早期神经元分化似乎完整。TuJ对开放神经管内的结构进行染色。运动神经元存在于腹角和腹根中。背根神经节存在,且大小与对照相似。染色模式与C57BL/6J对照小鼠相似,尽管在卷尾脊髓脊膜膨出中背侧结构向外侧移位。基于这个模型,在那些不存在神经组织固有遗传缺陷的病例中,修复人类脊髓脊膜膨出的胎儿手术可能会保留神经功能。