成年蛙脊髓背根轴突的再生。脊椎动物中枢神经系统再生模型。

F J Liuzzi, R J Lasek
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引用次数: 9

摘要

蛙背根为研究成年脊椎动物中枢神经系统轴突再生提供了一个有用的模型。我们使用该模型比较了在相同中枢神经系统环境下两种非常不同类型的轴突的再生,发现再生的背根和运动神经元轴突在脊髓中表现出相似的生长模式。感觉轴突和运动轴突在某些区域优先生长,而在其他区域则不优先生长。它们都能在背外侧神经束(DLF)内纵向和径向有效地再生。相反,感觉轴突和运动轴突在背索(DF)纵向或径向再生较少。两种截然不同的轴突种群的这种相似的优先生长表明,这种生长模式反映了脊髓细胞环境的区域差异。DLF具有由径向胶质突分离的无髓轴突束,背根损伤后呈轻度胶质性。相比之下,DF具有非常大的髓鞘轴突,它广泛地分隔穿过该区域的径向胶质突。背根损伤后,该区域明显胶质化,含有髓磷脂、碎片、少突胶质细胞和小胶质巨噬细胞。我们的数据表明,与髓鞘碎片、少突胶质细胞和巨噬细胞相比,无髓鞘轴突和径向胶质突是轴突生长的首选基质。因此,成年哺乳动物中枢神经系统中以大髓鞘轴突为特征的区域不能支持轴突生长就不足为奇了。此外,有证据表明,成年哺乳动物中枢神经系统中以无髓鞘轴突为特征的区域支持轴突生长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dorsal root axonal regeneration in the adult frog spinal cord. A model of vertebrate CNS regeneration.

The frog dorsal root provides a useful model for the study of axonal regeneration in an adult vertebrate CNS. We have used the model to compare the regeneration of two very different types of axons within the same CNS environment and have found that regenerating dorsal root, as well as rerouted motoneuron axons, display similar growth patterns in the spinal cord. Both sensory and motor axons grow preferentially in some regions and not in others. They both regenerate effectively longitudinally as well as radially within the dorsolateral fasciculus (DLF). By contrast, fewer sensory and motor axons regenerate longitudinally or radially in the dorsal funiculus (DF). This similar preferential growth of two very different populations of axons suggests that the growth patterns reflect regional differences in the cellular environment of the cord. The DLF has fascicles of unmyelinated axons separated by radial glial processes and, after dorsal root injury, is mildly gliotic. By contrast, DF has very large myelinated axons, which widely separate the radial glial processes that traverse the region. After dorsal root injury, this region is markedly gliotic and contains myelin, debris and oligodendroglia, and microglial macrophages. Our data suggest that unmyelinated axons and radial glial processes are more preferred substrates for axonal growth than myelin debris, oligodendroglia and macrophages. It is not surprising, then, that regions of the adult mammalian CNS that are characterized by large myelinated axons fail to support axonal growth. Moreover, there is some evidence that regions of the adult mammalian CNS that are characterized by unmyelinated axons support axonal growth.

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