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来自1A型夏科-马里-图斯病大鼠模型的长期背根神经节培养物中的轴突损伤和脱髓鞘

Axonal damage and demyelination in long-term dorsal root ganglia cultures from a rat model of Charcot-Marie-Tooth type 1A disease.

作者信息

Nobbio Lucilla, Gherardi Gianfranco, Vigo Tiziana, Passalacqua Mario, Melloni Edon, Abbruzzese Michele, Mancardi Gianluigi, Nave Klaus-Armin, Schenone Angelo

机构信息

Department of Neurosciences, Ophthalmology and Genetics, University of Genoa, Italy, Via De Toni, 5, 16132, Genoa, Italy.

出版信息

Eur J Neurosci. 2006 Mar;23(6):1445-52. doi: 10.1111/j.1460-9568.2006.04666.x.

Abstract

Clinical progression in hereditary and acquired demyelinating disorders of both the central and peripheral nervous system is mainly due to a time-dependent axonal impairment. We established 90-day dorsal root ganglia (DRG) cultures from a rat model of Charcot-Marie-Tooth type 1A (CMT1A) neuropathy to evaluate the structure of myelin and axons, and the expression of myelin-related proteins and cytoskeletal components, by morphological and molecular techniques. Both wild-type and CMT1A cultures were rich in myelinated fibres. Affected cultures showed dysmyelinated internodes and focal myelin swellings. Furthermore, uncompacted myelin and smaller axons with increased neurofilament (NF) density were found by electron microscopy, and Western blots showed higher levels of nonphosphorylated NF. Confocal microscopy demonstrated an abnormal distribution of the myelin-associated glycoprotein which, instead of being expressed at the noncompact myelin level, showed focal accumulation along the internodes while other myelin proteins were normally distributed. These findings suggest that CMT1A DRG cultures, similarly to the animal model and human disease, undergo axonal atrophy over a period of time. This model may be utilized to study the molecular changes underlying demyelination and secondary axonal impairment. As axonal damage may occur after just 3 months and tissue cultures represent a strictly controlled environment, this model may be ideal for testing neuroprotective therapies.

摘要

中枢和周围神经系统遗传性及获得性脱髓鞘疾病的临床进展主要归因于时间依赖性轴突损伤。我们从1A型腓骨肌萎缩症(CMT1A)神经病大鼠模型建立了90天的背根神经节(DRG)培养物,通过形态学和分子技术评估髓鞘和轴突的结构,以及髓鞘相关蛋白和细胞骨架成分的表达。野生型和CMT1A培养物中均富含髓鞘化纤维。受影响的培养物显示节间髓鞘形成异常和局灶性髓鞘肿胀。此外,通过电子显微镜发现了疏松的髓鞘和神经丝(NF)密度增加的较小轴突,蛋白质免疫印迹显示非磷酸化NF水平较高。共聚焦显微镜显示髓鞘相关糖蛋白分布异常,其并非在疏松髓鞘水平表达,而是沿节间呈局灶性积聚,而其他髓鞘蛋白分布正常。这些发现表明,CMT1A DRG培养物与动物模型和人类疾病相似,在一段时间内会发生轴突萎缩。该模型可用于研究脱髓鞘和继发性轴突损伤的潜在分子变化。由于仅3个月后就可能发生轴突损伤,且组织培养代表了一个严格受控的环境,因此该模型可能是测试神经保护疗法的理想选择。

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