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串珠状的起源与本质:神经纤维形状的可逆转变

The origin and nature of beading: a reversible transformation of the shape of nerve fibers.

作者信息

Ochs S, Pourmand R, Jersild R A, Friedman R N

机构信息

Department of Physiology and Biophysics, Indiana University School of Medicine, Indianapolis 46202, USA.

出版信息

Prog Neurobiol. 1997 Aug;52(5):391-426. doi: 10.1016/s0301-0082(97)00022-1.

Abstract

Nerve fibers which appear beaded (varicose, spindle-shaped, etc.) are often considered the result of pathology, or a preparation artifact. However, beading can be promptly elicited in fresh normal nerve by a mild stretch and revealed by fast-freezing and freeze-substitution, or by aldehyde fixating at a temperature near 0 degree C (cold-fixation). The key change in beading are the constrictions, wherein the axon is much reduced in diameter. Axoplasmic fluid and soluble components are shifted from the constrictions into the expansions leaving behind compacted microtubules and neurofilaments. Labeled cytoskeletal proteins carried down by slow axonal transport are seen to move with the soluble components and not to have been incorporated into and remain with, the cytoskeletal organelles on beading the fibers. Lipids and other components of the myelin sheath are also shifted from the constrictions into the expansions, with preservation of its fine structure and thickness. Additionally, myelin intrusions into the axons are produced and a localized bulging into the axon termed "leafing". The beading constrictions do not arise from the myelin sheath: beading occurs in the axons of unmyelinated fibers. It does not depend on the axonal cytoskeleton: exposure of nerves in vitro to beta, beta'-iminodipropionitrile (IDPN) disaggregates the cytoskeletal organelles and even augments beading. The hypothesis advanced was that the beading constrictions are due to the membrane skeleton; the subaxolemmal network comprised of spectrin/fodrin, actin, ankyrin, integrins and other transmembrane proteins. The mechanism can be activated directly by neurotoxins, metabolic changes, and by an interruption of axoplasmic transport producing Wallerian degeneration.

摘要

那些看起来呈串珠状(曲张、纺锤形等)的神经纤维通常被认为是病理结果或制备假象。然而,在新鲜的正常神经中,通过轻度拉伸可迅速引发串珠化,并通过快速冷冻和冷冻置换,或在接近0摄氏度的温度下醛固定(冷固定)来显示。串珠化的关键变化是缢缩,其中轴突直径大幅减小。轴浆流体和可溶性成分从缢缩处转移到膨大处,留下紧密排列的微管和神经丝。通过慢速轴突运输携带下来的标记细胞骨架蛋白与可溶性成分一起移动,而在串珠化纤维上并未整合到细胞骨架细胞器中并与之保留。髓鞘的脂质和其他成分也从缢缩处转移到膨大处,同时保持其精细结构和厚度。此外,还会产生髓鞘向轴突内的侵入以及向轴突内的局部膨出,称为“叶状化”。串珠化缢缩并非源于髓鞘:串珠化发生在无髓纤维的轴突中。它不依赖于轴突细胞骨架:体外将神经暴露于β,β'-亚氨基二丙腈(IDPN)会使细胞骨架细胞器解体,甚至增强串珠化。提出的假说是,串珠化缢缩是由于膜骨架;即由血影蛋白/肌动蛋白、肌动蛋白、锚蛋白、整合素和其他跨膜蛋白组成的轴膜下网络。该机制可直接由神经毒素、代谢变化以及轴浆运输中断导致华勒氏变性激活。

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