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微纤丝的结构、合成与取向。V. 关于从微管抑制剂处理中恢复独居卵囊的研究。

Structure, synthesis and orientation of microfibrils. V. On the recovery of Oocystis solitaria from microtubule inhibitor treatment.

作者信息

Quader H, Wagenbreth I, Robinson D G

出版信息

Cytobiologie. 1978 Oct;18(1):39-51.

PMID:568574
Abstract

Depending on the type of the inhibitor and its concentration one can experimentally induce two forms of aberrant microfibril orientations in O. solitaria cell walls through microtubule inhibitor application. The first form, designated "Intermediate", is characterized by the presence of cortical microtubules together with a spiral arrangement of microfibrils. The second form, designated "Parrallel", shows a wall with bundles of parallel oriented microfibrils without cortical microtubules. Taking colchicine as an example for a microtubule-inhibitor the "Parallel" form may be obtained with 10mM and the "Intermediate" with 5 to 1 mM solutions. Some microtubule-inhibitors such as methylbenzimidazole-2yl-carbamate (MBC) produce the "intermediate" form only. The recovery of normal microfibril orientation after inhibitor treatment is dependent on three factors: a) the developmental stage--young autospores just beginning to synthesize a wall are absolutely necessary; b) the application of inhibitors with the lowest effective concentration for c) the shortest possible time. Minimal concentrations for obtaining a "Full" effect range from 10 mM for colchicine to 1 micrometer for amiprophosmethyl (APM) with incubation periods from 3 to 9 hours. The return to the normal microfibril orientation has been achieved in all cases except after podophyllotoxin treatment. Since APM has been claimed to act selectively on tubulin synthesis in Chlamydomonas it was decided to compare the effects of this compound with cycloheximide (10 microgram/ml) on the recovery of microfibril orientation after colchicine treatment. In both cases no orientation recovery is possible although in the case of cycloheximide, synthesis of cellulose is drastically inhibited. This cycloheximide inhibition is fully reversible. During cycloheximide, but not APM, inhibition cortical microtubules return; however, due to the inhibition of cellulose synthesis itself, they cannot exert their orienting influence.

摘要

根据抑制剂的类型及其浓度,通过应用微管抑制剂,可在孤独小球藻细胞壁中实验性地诱导出两种形式的异常微纤丝取向。第一种形式称为“中间型”,其特征是存在皮质微管以及微纤丝的螺旋排列。第二种形式称为“平行型”,其细胞壁呈现出平行排列的微纤丝束,且没有皮质微管。以秋水仙碱作为微管抑制剂的例子,10mM的溶液可得到“平行型”,5至1mM的溶液可得到“中间型”。一些微管抑制剂,如甲基苯并咪唑 -2-基 - 氨基甲酸酯(MBC),只会产生“中间型”。抑制剂处理后正常微纤丝取向的恢复取决于三个因素:a)发育阶段——刚开始合成细胞壁的幼嫩自孢子是绝对必要的;b)以最低有效浓度应用抑制剂;c)尽可能短的时间。获得“完全”效果的最低浓度范围从秋水仙碱的10mM到胺丙畏(APM)的1微米,孵育时间为3至9小时。除鬼臼毒素处理后外,在所有情况下都已实现恢复到正常微纤丝取向。由于有人声称APM对衣藻中的微管蛋白合成有选择性作用,因此决定比较该化合物与环己酰亚胺(10微克/毫升)对秋水仙碱处理后微纤丝取向恢复的影响。在这两种情况下都不可能恢复取向,尽管在环己酰亚胺的情况下,纤维素的合成受到极大抑制。这种环己酰亚胺抑制是完全可逆的。在环己酰亚胺抑制期间,皮质微管会恢复,但由于纤维素合成本身受到抑制,它们无法发挥其定向影响,而APM抑制期间皮质微管不会恢复。

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