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施万细胞在去神经支配的运动终板和大鼠面神经横断后运动神经元中 B-50/GAP-43 的上调。

Upregulation of B-50/GAP-43 in Schwann cells at denervated motor endplates and in motoneurons after rat facial nerve crush.

机构信息

Laboratory for Neuromuscular Diseases, University of Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.

出版信息

Restor Neurol Neurosci. 1993 Jan 1;6(1):35-47. doi: 10.3233/RNN-1993-6104.

Abstract

Crush or transection of peripheral nerves of the adult rat is accompanied by changes in protein expression, including the growth associated protein (GAP-43) B-50. Following peripheral nerve crush in rat enhanced B-50 immunoreactivity was observed in regenerating nerve fibres and in newly formed axon terminals. However, before reinnervation was apparent, an unexpected transient increase in B-50 immunoreactivity was observed at denervated motor endplates [J. Neurosci. 8 (1988) 1759]. This study was performed to clarify this observation. Four days following facial nerve crush B-50 immunoreactivity was detected by double immunofluorescence microscopy in Sl00-positive Schwann cells covering the denervated endplates. Using diluted polyclonal and monoclonal B-50 antibodies we found that B-50 immunoreactivity at the denervated motor endplates was strongly increased in comparison to innervated motor endplates in which B-50 immunoreactivity was hardly detectable. However, when a high concentration of B-50 antibodies was applied the normal innervated motor endplates were also B-50 immunoreactive. Muscle fibres did not display B-50 immunoreactivity. Northern blot analysis revealed elevated B-50 mRNA in denervated muscle and in degenerating nerve with respect to the controls. The B-50 mRNA levels in these non-neuronal tissues were very low compared to the intact and injured facial nucleus containing the neuronal cell bodies. Electron microscopy demonstrated that the B-50 protein was localized in the processes of Schwann cells covering axon terminals of intact and vacant motor endplates and in axon varicosities of sympathetic nerves. This study has confirmed that prior to reinnervation B-50 immunoreactivity is increased at denervated motor endplates and shows that B-50 is co-localized with S100 in Schwann cells. Therefore, upregulation of B-50 expression in Schwann cells may explain the early occurrence of B-50 immunoreactivity at the motor endplate.

摘要

成年大鼠周围神经的挤压或横断伴随着蛋白质表达的变化,包括生长相关蛋白(GAP-43)B-50。在大鼠周围神经挤压后,再生神经纤维和新形成的轴突末端观察到 B-50 免疫反应性增强。然而,在重新支配之前,在去神经支配的运动终板上观察到 B-50 免疫反应性的意外短暂增加[J. Neurosci. 8(1988)1759]。本研究旨在阐明这一观察结果。面神经挤压后 4 天,通过 Sl00 阳性施万细胞覆盖的去神经运动终板上的双免疫荧光显微镜检测到 B-50 免疫反应性。使用稀释的多克隆和单克隆 B-50 抗体,我们发现与几乎检测不到 B-50 免疫反应性的神经支配运动终板相比,去神经运动终板上的 B-50 免疫反应性显著增加。然而,当应用高浓度的 B-50 抗体时,正常神经支配的运动终板也具有 B-50 免疫反应性。肌肉纤维不显示 B-50 免疫反应性。Northern blot 分析显示,与对照组相比,去神经支配的肌肉和退化神经中的 B-50 mRNA 升高。这些非神经组织中的 B-50 mRNA 水平与包含神经元细胞体的完整和损伤的面神经核相比非常低。电子显微镜显示 B-50 蛋白定位于覆盖完整和空的运动终板轴突末端的施万细胞的过程中和交感神经的轴突膨体中。本研究证实,在重新支配之前,去神经支配的运动终板上 B-50 免疫反应性增加,并表明 B-50 与施万细胞中的 S100 共定位。因此,施万细胞中 B-50 表达的上调可能解释了运动终板上 B-50 免疫反应性的早期发生。

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