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髓母细胞瘤神经胶质祖细胞延伸的细胞质突起中的微丝冠。

Crown of microfilaments in the extending cytoplasmic processes of medulloblastoma glial progenitors.

作者信息

Maria B L, Cumming R, Sukhu L

机构信息

Division of Neurology (Department of Pediatrics), University of Florida College of Medicine, Gainesville 32610-0296.

出版信息

Can J Neurol Sci. 1992 Feb;19(1):23-33.

PMID:1314124
Abstract

Microfilaments and microtubules play a part in the extension of neuronal processes but their roles in the formation of glial processes have not yet been determined. The objectives of this study were to determine the organization of microfilaments in differentiating glial progenitors (RB2 cells) and to study the effects of microfilament or microtubule disruption on process extension. Intense F-actin staining (crown of microfilaments) was observed at the leading edge of a small extending conical tip in differentiating RB2 cells, but was absent in process-bearing TE671 rhabdomyosarcoma cells. No significant difference was noted in the mean number of TE671 cells with processes treated with a microfilament disrupter from that of similarly treated controls. In contrast, a significant difference was noted in the mean number of RB2 cells with processes after microfilament disruption treatment from that of similarly treated controls. Microtubule disruption arrested extension and caused process retraction in both cell types. The results of this study demonstrate that microtubules play an equally important part in the extension and stabilization of the RB2 and TE671 processes. Moreover, the crown of microfilaments concentrated in the glial RB2 process (and not in the TE671 process) may be critical to its extension during differentiation.

摘要

微丝和微管在神经元突起的延伸中发挥作用,但它们在胶质细胞突起形成中的作用尚未确定。本研究的目的是确定分化中的胶质前体细胞(RB2细胞)中微丝的组织情况,并研究微丝或微管破坏对突起延伸的影响。在分化的RB2细胞中,在一个小的延伸锥形尖端的前沿观察到强烈的F-肌动蛋白染色(微丝冠),但在有突起的TE671横纹肌肉瘤细胞中未观察到。用微丝破坏剂处理的有突起的TE671细胞的平均数量与同样处理的对照组相比没有显著差异。相反,微丝破坏处理后有突起的RB2细胞的平均数量与同样处理的对照组相比有显著差异。微管破坏会阻止两种细胞类型的突起延伸并导致突起回缩。本研究结果表明,微管在RB2和TE671细胞突起的延伸和稳定中发挥着同样重要的作用。此外,集中在胶质RB2细胞突起(而非TE671细胞突起)中的微丝冠可能对其分化过程中的延伸至关重要。

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