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泰耶普大鼠髓鞘形成缺陷的时间进程。

The temporal progression of the myelination defect in the taiep rat.

作者信息

Lunn K F, Clayton M K, Duncan I D

机构信息

Department of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison 53706, USA.

出版信息

J Neurocytol. 1997 May;26(5):267-81. doi: 10.1023/a:1018548400536.

Abstract

The Sprague Dawley myelin mutant, the taiep rat, demonstrates a defect in CNS myelination which worsens with age and which is associated with abnormal accumulations of microtubules in oligodendrocytes. Quantitative and qualitative electron microscopic studies of myelin development and oligodendrocyte morphology were used to describe the temporal development of the defect in this mutant, in three regions of the CNS. The results indicate that the time of onset of myelination is similar in mutant and control rats, however the amount of myelin formed is reduced in the mutant, compared to controls, and there is a loss of myelin from the taiep CNS as the animals age. Thus the myelination defect in taiep has features of both hypomyelination and demyelination. Oligodendrocyte microtubule abnormalities were noted in each region of the taiep CNS at the time of onset of myelination. The earliest changes seen were close associations of oligodendrocyte microtubules with endoplasmic reticulum, with marked accumulations of microtubules filling the cytoplasm of oligodendrocytes from older taiep rats. These findings suggest that the microtubule abnormality in the taiep mutant inhibits both the initial formation and the long-term maintenance of myelin by the oligodendrocyte. In addition, there is also evidence to suggest that although the microtubule abnormality is present in oligodendrocytes throughout the taiep CNS, it results in a more marked defect in the myelination of axons of small diameter.

摘要

斯普拉格-道利髓磷脂突变体——泰耶普大鼠,表现出中枢神经系统髓鞘形成缺陷,该缺陷会随着年龄增长而恶化,且与少突胶质细胞中微管的异常积聚有关。利用对髓鞘发育和少突胶质细胞形态的定量和定性电子显微镜研究,来描述该突变体在中枢神经系统三个区域中缺陷的时间发展情况。结果表明,突变大鼠和对照大鼠的髓鞘形成起始时间相似,然而,与对照相比,突变体形成的髓鞘量减少,并且随着动物年龄增长,泰耶普大鼠中枢神经系统中的髓鞘会丢失。因此,泰耶普大鼠的髓鞘形成缺陷具有髓鞘形成不足和脱髓鞘的特征。在髓鞘形成开始时,在泰耶普大鼠中枢神经系统的每个区域都观察到少突胶质细胞微管异常。最早出现的变化是少突胶质细胞微管与内质网紧密相连,来自老年泰耶普大鼠的少突胶质细胞胞质中充满了大量微管积聚。这些发现表明,泰耶普突变体中的微管异常抑制了少突胶质细胞对髓鞘的初始形成和长期维持。此外,也有证据表明,尽管整个泰耶普大鼠中枢神经系统的少突胶质细胞中都存在微管异常,但它导致小直径轴突的髓鞘形成出现更明显的缺陷。

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