Gordon P, Carpentier J L, Van Obberghen E, Barazzone P, Roth J, Orci L
J Cell Sci. 1979 Oct;39:77-88. doi: 10.1242/jcs.39.1.77.
When cultured human lymphocytes (IM-9) are exposed to 10(-6) M procine insulin for 6 h, washed, and incubated with 125I-insulin, the ability of the cell to bind the labelled hormone is reduced by a mean of 78%. Under these experimental conditions that induce insulin-receptor loss in this cell there is a mean 95% increase in microinvaginations in the plasma membrane revealed by electron microscopy on freez-fractured replicas of the cell. At the same time, horseradish peroxidase uptake, a marker of endocytosis, is increased in the cells incubated with insulin. Coupled with our recent EM autoradiographic evidence that labelled insulin is acutely internalized by this cell, these studies are consistent with the possibility that endocytosis represents a mechanism by which receptor is removed from the cell surface.
当培养的人淋巴细胞(IM - 9)暴露于10⁻⁶ M猪胰岛素6小时,洗涤后再与¹²⁵I - 胰岛素孵育时,细胞结合标记激素的能力平均降低78%。在这些导致该细胞胰岛素受体丧失的实验条件下,通过对细胞冷冻断裂复制品进行电子显微镜观察发现,质膜中的微内陷平均增加了95%。同时,与胰岛素孵育的细胞中,作为内吞作用标志物的辣根过氧化物酶摄取增加。结合我们最近的电子显微镜放射自显影证据,即标记的胰岛素可被该细胞迅速内化,这些研究结果与内吞作用是一种将受体从细胞表面移除的机制这一可能性相一致。