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

Cytobiologie Pub Date : 1978-10-01
H Quader, I Wagenbreth, D G Robinson
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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.

微原纤维的结构、合成和取向。五、微管抑制剂对孤卵囊虫的恢复作用。
根据抑制剂的类型及其浓度,可以通过微管抑制剂的应用在实验中诱导两种形式的异常微纤维取向。第一种形式被称为“中间”,其特征是皮层微管的存在以及微原纤维的螺旋排列。第二种形式,称为“平行”,显示了一束平行定向的微原纤维的壁,没有皮质微管。以秋水仙碱作为微管抑制剂为例,用10mM溶液可以得到“平行”形式,用5 ~ 1mm溶液可以得到“中间”形式。一些微管抑制剂,如甲基苯并咪唑-2酰基氨基甲酸酯(MBC)只产生“中间”形式。抑制剂处理后微原纤维的正常取向的恢复取决于三个因素:a)发育阶段——刚开始合成壁的年轻auto孢子是绝对必要的;B)使用最低有效浓度的抑制剂c)尽可能短的时间。获得“完全”效应的最小浓度范围为秋水仙碱10毫米至氨丙磷甲基(APM) 1微米,潜伏期为3至9小时。除鬼臼毒素治疗外,所有病例均可恢复到正常的微纤维取向。由于APM已被认为对衣藻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亚胺(10微克/毫升)在秋水仙碱处理后对微纤维定向恢复的影响。在这两种情况下,没有取向恢复是可能的,尽管在环己亚胺的情况下,纤维素的合成被大大抑制。这种环己亚胺抑制作用是完全可逆的。环己亚胺抑制皮质微管回流,APM不抑制;然而,由于纤维素合成本身的抑制作用,它们无法发挥定向作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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