Involvement of neurofilaments in the radial growth of axons.

D W Cleveland, M J Monteiro, P C Wong, S R Gill, J D Gearhart, P N Hoffman
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引用次数: 82

Abstract

The control of radial growth of axons is of functional importance because caliber is a principal determinant of conduction velocity in myelinated nerve fibers. Neurofilaments, the major cytoskeletal protein in myelinated nerves, appear to be intrinsic determinants of caliber. Evidence supporting this derives first from the linear relationship between neurofilament content and axonal diameter. Further, following distal axonal injury in a peripheral nerve, caliber is reduced in the proximal axonal stumps. This reduction in caliber is itself due to selective suppression of neurofilament gene expression, thereby leading to lower levels of newly synthesized neurofilament subunits transported into the axon and a consequent decrease in axonal neurofilament content. To demonstrate directly the physiological consequence of altering normal neurofilament accumulation, we have elevated neurofilament expression by introducing additional genes into transgenic mice. The clear result is that increases in NF-L content alone are not sufficient to increase axonal caliber. To test the consequence of disruption of normal filament accumulation, we have identified dominant assembly-disrupting mutants in NF-L and NF-M and have used these to produce transgenic animals in which neurofilament assembly should be disrupted.

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神经丝参与轴突的径向生长。
轴突径向生长的控制具有重要的功能,因为直径是髓鞘神经纤维传导速度的主要决定因素。神经丝是髓鞘神经中主要的细胞骨架蛋白,似乎是直径的内在决定因素。支持这一观点的证据首先来自于神经丝含量和轴突直径之间的线性关系。此外,外周神经远端轴突损伤后,近端轴突残端直径减小。这种口径的减少本身是由于神经丝基因表达的选择性抑制,从而导致新合成的神经丝亚基转运到轴突的水平降低,从而导致轴突神经丝含量的减少。为了直接证明改变正常神经丝积累的生理后果,我们通过向转基因小鼠中引入额外的基因来提高神经丝的表达。明确的结果是,单纯增加NF-L含量不足以增加轴突口径。为了测试破坏正常纤维积累的后果,我们在NF-L和NF-M中确定了显性组装破坏突变体,并利用这些突变体生产了神经丝组装应该被破坏的转基因动物。
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Studies of DNA methylation in animals. Characterization of the execution phase of apoptosis in vitro using extracts from condemned-phase cells. Analysis of the temporal program of replication initiation in yeast chromosomes. On the structure of replication and transcription factories. Stepwise assembly of initiation complexes at budding yeast replication origins during the cell cycle.
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