Carpentier J L, Gorden P, Freychet P, Canivet B, Orci L
Endocrinology. 1981 Sep;109(3):768-75. doi: 10.1210/endo-109-3-768.
When [125I]iodoepidermal growth factor is incubated with freshly isolated rat hepatocytes, cell-associated radioactivity reaches apparent steady state by 60 min at 20 C and by 30 min of incubation at 37 C. When the distribution of cell-associated radioactivity is studied at different times of incubation by quantitative electron microscopic autoradiography, the ligand initially associates with the plasma membrane and is progressively internalized as a function of time. The internalized ligand preferentially associates with lysosome-like structures. Qualitatively, these events are similar to those previously obtained with labeled insulin and glucagon in this cell, but quantitatively, the internalization of epidermal growth factor is much greater. The data suggest that the ligand or its specific receptor rather than the cell type is the major determinant of the rate of internalization.
当将[125I]碘表皮生长因子与新鲜分离的大鼠肝细胞一起孵育时,在20℃下60分钟以及在37℃下孵育30分钟时,细胞相关放射性达到明显的稳态。当通过定量电子显微镜放射自显影术在不同孵育时间研究细胞相关放射性的分布时,配体最初与质膜结合,并随着时间的推移逐渐内化。内化的配体优先与溶酶体样结构结合。定性地说,这些事件与之前在这种细胞中用标记的胰岛素和胰高血糖素所获得的事件相似,但定量地说,表皮生长因子的内化程度要大得多。数据表明,配体或其特异性受体而非细胞类型是内化速率的主要决定因素。