Bergeron J J, Resch L, Rachubinski R, Patel B A, Posner B I
J Cell Biol. 1983 Mar;96(3):875-86. doi: 10.1083/jcb.96.3.875.
Binding and internalization of 125I-ovine prolactin into hepatocytes of female rats was visualized by the in vivo radioautographic method (Bergeron, J. J. M., G. Levine, R. Sikstrom, D. O'Shaughnessey, B. Kopriwa, N. J. Nadler, and B. I. Posner, 1977, Proc. Natl. Acad. Sci. USA, 745:051-5055). Receptor-mediated internalization of label was observed into lipoprotein-filled vesicles in the Golgi/bile canalicular region of the hepatocyte. Colchicine treatment had no effect on the internalization of label into the lipoprotein-filled vesicles. However, the location of the radio-labeled lipoprotein-filled vesicles was altered from the Golgi/bile canalicular region to subsinusoidal. Radioactive content of hepatocytes decreased as a function of time after injection of 125I-prolactin; however, colchicine treatment markedly retarded this loss of label. Subcellular fractionation experiments indicated that colchicine treatment led to decreased levels of 125I-prolactin accumulation in microsomes but augmented the accumulation of label in the L fraction. It is concluded that in normal female rats prolactin is internalized into lipoprotein-filled vesicles in the Golgi region before degradation of the hormone. Colchicine treatment accumulates labeled lipoprotein-containing vesicles in a subsinusoidal region and retards hormone catabolism. The labeled vesicles observed after colchicine treatment may correspond to the unique vesicles previously observed in the L fraction and found to be enriched in prolactin receptors (Khan, M. N., B. I. Posner, A. K. Verma, R. J. Khan, and J. J. M. Bergeron, 1981, Proc. Natl. Acad. Sci. USA, 78:4980-4981).
采用体内放射自显影法(伯杰龙,J. J. M.,G. 莱文,R. 西克斯特伦,D. 奥肖内西,B. 科普里瓦,N. J. 纳德勒,以及B. I. 波斯纳,1977年,《美国国家科学院院刊》,745:051 - 5055)观察了125I - 绵羊催乳素在雌性大鼠肝细胞中的结合与内化情况。在肝细胞的高尔基体/胆小管区域,观察到标记物通过受体介导被内化到充满脂蛋白的囊泡中。秋水仙碱处理对标记物内化到充满脂蛋白的囊泡中没有影响。然而,放射性标记的充满脂蛋白的囊泡的位置从高尔基体/胆小管区域改变到了肝血窦周隙。注射125I - 催乳素后,肝细胞的放射性含量随时间下降;然而,秋水仙碱处理显著延缓了标记物的这种损失。亚细胞分级分离实验表明,秋水仙碱处理导致微粒体中125I - 催乳素积累水平降低,但增加了L组分中标记物的积累。结论是,在正常雌性大鼠中,催乳素在激素降解之前被内化到高尔基体区域充满脂蛋白的囊泡中。秋水仙碱处理使含有标记脂蛋白的囊泡在肝血窦周隙区域积累,并延缓激素分解代谢。秋水仙碱处理后观察到的标记囊泡可能与先前在L组分中观察到的独特囊泡相对应,并且发现这些囊泡富含催乳素受体(汗,M. N.,B. I. 波斯纳,A. K. 维尔马,R. J. 汗,以及J. J. M. 伯杰龙,1981年,《美国国家科学院院刊》,78:4980 - 4981)。