Rudd C E, Rogers K A, Brown D L, Kaplan J G
Can J Biochem. 1979 Jun;57(6):673-83. doi: 10.1139/o79-085.
We have studied the time course of disassembly of microtubules of resting and stimulated mouse lymphocytes caused by the drug colchicine, as well as the effect of this compound on DNA and RNA synthesis of human and mouse lymphocytes. Fine-structure studies with the electron microscope showed a great increase in number of microtubules resulting from stimulation of mouse lymphocytes by the mitogenic lectin Con A. The presence of a network of microtubules was demonstrated in resting lymphocytes by use of the technique of immunofluorescence; this technique was not effective for the study of the microtubules of stimulated lymphocytes in the blast stage. The disappearance of microtubular networks in some cells (approximately 25%) was caused by the protocol of colchicine treatment used in many laboratories (30 min at 10(6) M); a 6- to 8-h treatment was required to cause all cells to lose their microtubules. It is indicated in these findings that there is need for extreme caution in implicating microtubule disruption as the cause of certain colchicine effects, such as that on the Con A-induced inhibition of receptor-ligand migration. The addition of colchicine to stimulated cells at varying times of culture caused marked inhibition of DNA synthesis provided that sufficient time (approximately 20 h for maximum inhibition) elapsed between addition of the drug to the stimulated culture and assay of DNA synthesis. Our data on the time course of inhibition of DNA synthesis by alpha-methyl mannoside (alpha MM) and by colchicine do not exclude the possibility that the latter compound may act partially by affecting the commitment of stimulated lymphocytes to DNA synthesis but they show that it can inhibit well after commitment is complete. The later the time of assay of thymidine incorporation, the more disparate were the curves relating the effects of alpha MM and colchicine to DNA synthesis of human cells. In the case of mouse splenic lymphocytes, there was no resemblance between the time course of the alpha MM and of the colchicine effects. Synthesis of RNA after 12 h of culture of stimulated human lymphocytes was also sensitive to colchicine.
我们研究了秋水仙碱对静止和受刺激的小鼠淋巴细胞微管解聚的时间进程,以及该化合物对人和小鼠淋巴细胞DNA和RNA合成的影响。用电子显微镜进行的精细结构研究表明,促有丝分裂凝集素Con A刺激小鼠淋巴细胞后,微管数量大幅增加。利用免疫荧光技术在静止淋巴细胞中证实了微管网络的存在;该技术对处于母细胞阶段的受刺激淋巴细胞的微管研究无效。许多实验室采用的秋水仙碱处理方案(10⁻⁶ M处理30分钟)导致一些细胞(约25%)的微管网络消失;需要6至8小时的处理才能使所有细胞失去微管。这些研究结果表明,在将微管破坏归咎于秋水仙碱的某些作用(如对Con A诱导的受体-配体迁移的抑制作用)时,需要极其谨慎。在培养的不同时间向受刺激细胞中添加秋水仙碱,只要在向受刺激培养物中添加药物与DNA合成检测之间经过足够的时间(最大抑制约需20小时),就会显著抑制DNA合成。我们关于α-甲基甘露糖苷(α-MM)和秋水仙碱抑制DNA合成的时间进程的数据并不排除后一种化合物可能部分通过影响受刺激淋巴细胞向DNA合成的转化起作用,但它们表明在转化完成后它仍能很好地发挥抑制作用。胸苷掺入检测的时间越晚,α-MM和秋水仙碱对人细胞DNA合成影响的曲线差异就越大。对于小鼠脾淋巴细胞,α-MM和秋水仙碱作用的时间进程没有相似之处。受刺激的人淋巴细胞培养12小时后的RNA合成也对秋水仙碱敏感。