Rudd C E, Kaplan J G
J Immunol. 1981 Apr;126(4):1640-3.
Concanavalin A (Con A) was found to induce the appearance of time-dependent and saturable thymidine transport in human peripheral lymphocytes with a Km that ranged from 200 to 500 microM and a Vmax of between 5 to 8 pmols/cell/sec; transport of thymidine could not be demonstrated in resting cultures. Colchicine was found to cause the disappearance of microtubular networks in the majority of cells in the population, whereas lumicolchicine as expected had no significant effect on the presence of microtubules. Lumicolchicine caused 50% inhibition of thymidine transport and of DNA synthesis at a concentration of about 10(-4) M; the effect of this agent on the transport of thymidine could account for its ability to inhibit DNA synthesis. Colchicine also inhibited the transport of thymidine by 50% at about 10(-4) M. However, half-maximal DNA synthesis occurred at a colchicine concentration of 5.0 X 10(-8) M; thus, the effect of this drug on transport cannot account for its effect on DNA synthesis, since the latter process is some 3 orders of magnitude more sensitive than the former. The ability of colchicine to inhibit DNA synthesis in Con A-stimulated human lymphocytes would appear to be an indirect consequence of disassembly of microtubules.
发现伴刀豆球蛋白A(Con A)可诱导人外周血淋巴细胞出现时间依赖性和可饱和的胸苷转运,其米氏常数(Km)范围为200至500微摩尔,最大反应速度(Vmax)为5至8皮摩尔/细胞/秒;在静止培养物中未检测到胸苷转运。发现秋水仙碱可导致群体中大多数细胞的微管网络消失,而光秋水仙碱正如预期的那样对微管的存在没有显著影响。光秋水仙碱在浓度约为10^(-4) M时可使胸苷转运和DNA合成受到50%的抑制;该药物对胸苷转运的影响可解释其抑制DNA合成的能力。秋水仙碱在约10^(-4) M时也可使胸苷转运受到50%的抑制。然而,DNA合成的半数最大效应发生在秋水仙碱浓度为5.0×10^(-8) M时;因此,该药物对转运的影响无法解释其对DNA合成的影响,因为后一过程比前一过程敏感约3个数量级。秋水仙碱抑制Con A刺激的人淋巴细胞中DNA合成的能力似乎是微管解聚的间接结果。