Kessel R G, Katow H
J Morphol. 1984 Mar;179(3):263-71. doi: 10.1002/jmor.1051790305.
The anterior limb bud mesenchyme cells of stage 24 chick embryos were dissociated by trypsinization followed by gentle pipetting, and placed in a tissue culture medium of F12 containing 10% fetal calf serum and antibiotics. As the cells became nearly confluent, some of them were exposed to colchicine or vinblastine sulfate for durations as long as 48 hr. The control and antitubulin-treated cells were processed for transmission electron microscopy and the ultrastructure of the cells was compared. Annulate lamellae (AL) were observed in small amounts in both control and antitubulin-treated cells. The amount of AL did not markedly differ in the control versus antitubulin-treated cells. Furthermore, few multinucleated cells were observed in antitubulin-treated cultures. These results indicate that prolonged culture of cells in antitubulins need not, in itself, lead to a condition of enhanced AL development as reported in several other studies using various cell types.
将24期鸡胚的前肢芽间充质细胞用胰蛋白酶消化,然后轻柔吹打使其解离,置于含有10%胎牛血清和抗生素的F12组织培养基中。当细胞接近汇合时,其中一些细胞暴露于秋水仙碱或硫酸长春碱中长达48小时。对对照细胞和抗微管蛋白处理的细胞进行透射电子显微镜处理,并比较细胞的超微结构。在对照细胞和抗微管蛋白处理的细胞中均观察到少量环孔板(AL)。对照细胞与抗微管蛋白处理的细胞中AL的数量没有明显差异。此外,在抗微管蛋白处理的培养物中观察到的多核细胞很少。这些结果表明,与其他几项使用各种细胞类型的研究报道不同,在抗微管蛋白中长时间培养细胞本身并不一定会导致环孔板发育增强的情况。