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转基因小鼠中髓鞘形成不足的施万细胞对轴突直径和神经丝的调节作用。

Modulation of axon diameter and neurofilaments by hypomyelinating Schwann cells in transgenic mice.

作者信息

Cole J S, Messing A, Trojanowski J Q, Lee V M

机构信息

Department of Pathology and Laboratory Medicine, University of Pennsylvania Medical School, Philadelphia 19104.

出版信息

J Neurosci. 1994 Nov;14(11 Pt 2):6956-66. doi: 10.1523/JNEUROSCI.14-11-06956.1994.

Abstract

Studies of peripheral nerves in two different lines of hypomyelinating transgenic mice support the hypothesis that myelinating Schwann cells exert a significant influence on key biological properties of axons. The mice contain transgenes combining the peripheral myelin protein zero gene (P0) promoter and either the diphtheria toxin A chain gene product or the SV40 (simian virus 40) large T antigen. The consequences of peripheral nerve hypomyelination on axon diameter, neurofilament (NF) density, and NF phosphorylation were analyzed. The sciatic nerves of the P0 diphtheria toxin A transgenic mice (DT) evidenced the most severe hypomyelination, and this was associated with a dramatic decrease in NF phosphorylation plus a marked increase in NF density. In contrast, the sciatic nerves in the P0 SV40 large T antigen transgenic mice (SV40) were not as severely hypomyelinated and there was a milder decrease in NF phosphorylation plus a more modest increase in NF density. Further, the sciatic nerves in both lines evidenced a decrease in axonal caliber without any change in NF content. Taken together, these studies provide strong evidence indicating that myelinating Schwann cells exert a significant influence on axon caliber by modulating NF phosphorylation and NF packing density in the axons of peripheral nerves. Thus, key biological properties of axons are modulated by signals transmitted from myelinating Schwann cells to axons of peripheral nerves.

摘要

对两种不同品系的少髓鞘转基因小鼠的外周神经研究支持了这样一种假说,即形成髓鞘的施万细胞对轴突的关键生物学特性有重大影响。这些小鼠含有将外周髓鞘蛋白零基因(P0)启动子与白喉毒素A链基因产物或猴病毒40(SV40)大T抗原相结合的转基因。分析了外周神经少髓鞘对轴突直径、神经丝(NF)密度和NF磷酸化的影响。P0白喉毒素A转基因小鼠(DT)的坐骨神经表现出最严重的少髓鞘,这与NF磷酸化的显著降低以及NF密度的显著增加有关。相比之下,P0 SV40大T抗原转基因小鼠(SV40)的坐骨神经少髓鞘程度没有那么严重,NF磷酸化的降低较轻微,NF密度的增加也较适度。此外,两个品系的坐骨神经都显示轴突管径减小,而NF含量没有任何变化。综上所述,这些研究提供了有力证据,表明形成髓鞘的施万细胞通过调节外周神经轴突中的NF磷酸化和NF堆积密度,对轴突管径有重大影响。因此,轴突的关键生物学特性受到从形成髓鞘的施万细胞传递到外周神经轴突的信号的调节。

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