Department of Neurology, Division of Neuroscience and INSPE, Neuropathology Unit, Milan, Italy.
Glia. 2010 Dec;58(16):2005-16. doi: 10.1002/glia.21069.
Numerous transgenic and knockout mouse models of human hereditary neuropathies have become available over the past decade. We describe a simple, reproducible, and safe biopsy of mouse skin for histopathological evaluation of the peripheral nervous system (PNS) in models of hereditary neuropathies. We compared the diagnostic outcome between sciatic nerve and dermal nerves found in skin biopsy (SB) from the hind foot. A total of five animal models of different Charcot-Marie-Tooth neuropathies, and one model of congenital muscular dystrophy associated neuropathy were examined. In wild type mice, dermal nerve fibers were readily identified by immunohistochemistry, light, and electron microscopy and they appeared similar to myelinated fibers in sciatic nerve. In mutant mice, SB manifested myelin abnormalities similar to those observed in sciatic nerves, including hypomyelination, onion bulbs, myelin outfolding, redundant loops, and tomacula. In many strains, however, SB showed additional abnormalities--fiber loss, dense neurofilament packing with lower phosphorylation status, and axonal degeneration-undetected in sciatic nerve, possibly because SB samples distal nerves. SB, a reliable technique to investigate peripheral neuropathies in human beings, is also useful to investigate animal models of hereditary neuropathies. Our data indicate that SB may reveal distal axonal pathology in mouse models and permits sequential follow-up of the neuropathy in an individual mouse, thereby reducing the number of mice necessary to document pathology of the PNS.
在过去的十年中,已经出现了许多用于研究人类遗传性神经病的转基因和基因敲除小鼠模型。我们描述了一种简单、可重复且安全的方法,用于从小鼠皮肤活检中获取组织病理学评估遗传性神经病模型中周围神经系统(PNS)的方法。我们比较了后脚皮肤活检(SB)中的坐骨神经和真皮神经的诊断结果。共检查了五种不同的腓骨肌萎缩症(Charcot-Marie-Tooth neuropathy)的动物模型和一种先天性肌营养不良症相关神经病的模型。在野生型小鼠中,真皮神经纤维通过免疫组织化学、光镜和电镜很容易被识别,并且它们与坐骨神经中的有髓纤维相似。在突变型小鼠中,SB 表现出类似于在坐骨神经中观察到的髓鞘异常,包括少突胶质细胞减少、洋葱球、髓鞘折叠、冗余环和 tomacula。然而,在许多品系中,SB 显示出额外的异常——纤维丢失、神经丝致密包装且磷酸化状态较低,以及轴突变性——在坐骨神经中未检测到,这可能是因为 SB 样本取自末梢神经。SB 是一种研究人类周围神经病的可靠技术,也可用于研究遗传性神经病的动物模型。我们的数据表明,SB 可能会揭示小鼠模型中的远端轴突病理学,并允许对单个小鼠的神经病进行连续随访,从而减少记录 PNS 病理学所需的小鼠数量。