Hugon J S, Bennett G, Pothier P, Ngoma Z
Cell Tissue Res. 1987 Jun;248(3):653-62. doi: 10.1007/BF00216496.
Explants from mouse jejunum were cultured for 3-7 h in the absence (control) or presence of colchicine (100 micrograms/ml) or nocodazole (10 micrograms/ml). In recovery experiments, explants were cultured in fresh medium for an additional period. To label glycoproteins, 3H-fucose was added during the last 3 or 6 h of the initial culture or recovery period. Subcellular fractionation studies revealed that colchicine and nocodazole inhibited migration of labelled glycoproteins to the brush border (P2) by 40-45%. Radioautographic studies of absorptive cells showed that colchicine and nocodazole inhibited labelling of the microvillous border by 67% and 87%, while labelling of the basolateral plasma membrane increased by 114% and 275%. Immunocytochemical studies revealed that both colchicine and nocodazole caused the virtual disappearance of the microtubular network in the absorptive cells. It is possible that some glycoproteins normally destined for the microvillous border are rerouted to the basolateral membrane. The observed loss of microtubules after drug treatment suggests that microtubules may play a role in the intracellular migration of membrane glycoproteins. Additional support for this concept is provided by the fact that in recovery experiments the distribution of label returned to control values after the microtubular network became re-established.
将小鼠空肠外植体在无(对照)或有秋水仙碱(100微克/毫升)或诺考达唑(10微克/毫升)的情况下培养3 - 7小时。在恢复实验中,将外植体在新鲜培养基中再培养一段时间。为标记糖蛋白,在初始培养或恢复期的最后3或6小时加入3H - 岩藻糖。亚细胞分级分离研究表明,秋水仙碱和诺考达唑使标记糖蛋白向刷状缘(P2)的迁移受到40 - 45%的抑制。对吸收细胞的放射自显影研究显示,秋水仙碱和诺考达唑使微绒毛边缘的标记受到67%和87%的抑制,而基底外侧质膜的标记分别增加了114%和275%。免疫细胞化学研究表明,秋水仙碱和诺考达唑均导致吸收细胞中微管网络几乎消失。一些通常运往微绒毛边缘的糖蛋白可能被重新导向基底外侧膜。药物处理后观察到的微管损失表明微管可能在膜糖蛋白的细胞内迁移中起作用。恢复实验中微管网络重新建立后标记分布恢复到对照值这一事实为这一概念提供了进一步支持。