Zimmermann H P, Faulstich H, Hänsch G M, Doenges K H, Stournaras C
Institute of Cell and Tumor Biology, German Cancer Research Center, Heidelberg.
Mutat Res. 1988 Oct;201(2):293-302. doi: 10.1016/0027-5107(88)90018-8.
The impact of triethyl lead chloride was studied on: (i) the in vitro assembly and disassembly of microtubules from porcine brain by turbidometry and electron microscopy, (ii) the microtubule system of living mammalian cells using immunofluorescence microscopy, (iii) cell motility and chemotaxis employing the methods of phagokinetic track formation and the Boyden chamber assay, respectively, and (iv) thiol groups of the protein tubulin by their titration in the presence and absence of the organic lead compound. Triethyl lead chloride inhibited microtubule assembly and depolymerized preformed microtubules in vitro and in living cells. Random motility of cells was not markedly inhibited by triethyl lead chloride, whereas chemotaxis (directed cellular movement) was strongly inhibited. Triethyl lead chloride was found to interact with 2 thiol groups of the tubulin dimer. The interaction of triethyl lead chloride with the tubulin/microtubule system in vivo likely causes aneuploidy and is at least partly responsible for the cytotoxicity of the drug.
(i)通过比浊法和电子显微镜观察猪脑微管在体外的组装和解聚;(ii)使用免疫荧光显微镜观察活的哺乳动物细胞的微管系统;(iii)分别采用吞噬运动轨迹形成法和博伊登小室分析法研究细胞运动性和趋化性;(iv)通过在有和没有有机铅化合物存在的情况下对微管蛋白的滴定来研究其巯基。三乙基氯化铅在体外和活细胞中均抑制微管组装并使预先形成的微管解聚。三乙基氯化铅并未显著抑制细胞随机运动,而强烈抑制趋化性(细胞定向运动)。发现三乙基氯化铅与微管蛋白二聚体的2个巯基相互作用。三乙基氯化铅在体内与微管蛋白/微管系统的相互作用可能导致非整倍体,并且至少部分地是该药物细胞毒性的原因。