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玻璃体内注射肿瘤坏死因子后完整小鼠视神经中少突胶质细胞的形态学变化

Morphological changes in oligodendrocytes in the intact mouse optic nerve following intravitreal injection of tumour necrosis factor.

作者信息

Butt A M, Jenkins H G

机构信息

Sherrington School of Physiology, UMDS, St. Thomas's Hospital, London, UK.

出版信息

J Neuroimmunol. 1994 Apr;51(1):27-33. doi: 10.1016/0165-5728(94)90125-2.

Abstract

Intracellular dye-injection was used to determine the whole-cell morphology of oligodendrocytes in intact optic nerves of mice following intravitreal injection of tumour necrosis factor-alpha (TNF alpha) or heat-inactivated TNF alpha to act as controls. Oligodendrocytes in control nerves had a stereotypic morphology, and provided an average of 20 axons with single internodal myelin segments of around 200 microns internodal length. Oligodendrocytes with abnormal morphological features were identified 8-14 days following intravitreal injection of TNF alpha. Internodal myelin segments developed swellings along their lengths, became attenuated, and in extreme cases receded completely. This study provides a new insight into the process of demyelination, especially of the early stages which are not amenable with other techniques. Furthermore, it confirms that injection of TNF alpha into the vitreous, a fluid compartment of the CNS, instigates a sequence of events which results in oligodendrocyte disruption and demyelination. The mechanism by which intravitreally injected TNF alpha mediates these changes in optic nerve oligodendrocytes are yet unknown.

摘要

采用细胞内染料注射法,在向小鼠玻璃体内注射肿瘤坏死因子-α(TNFα)或作为对照的热灭活TNFα后,确定完整视神经中少突胶质细胞的全细胞形态。对照神经中的少突胶质细胞具有刻板形态,平均为20条轴突提供单个节间髓鞘段,节间长度约为200微米。在玻璃体内注射TNFα后8 - 14天,可识别出具有异常形态特征的少突胶质细胞。节间髓鞘段沿其长度出现肿胀,变得变薄,在极端情况下完全退缩。这项研究为脱髓鞘过程,尤其是其他技术无法检测的早期阶段,提供了新的见解。此外,它证实了将TNFα注入中枢神经系统的液体腔室玻璃体中,会引发一系列导致少突胶质细胞破坏和脱髓鞘的事件。玻璃体内注射的TNFα介导视神经少突胶质细胞这些变化的机制尚不清楚。

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